63 results on '"Pennathur, Arjun"'
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2. Contributors
- Author
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Abbott, Brian G., primary, Abbott, J. Dawn, additional, Adams, David H., additional, Al-Atassi, Talal, additional, Al-Dameh, Ali, additional, Allen, Mark S., additional, Altorki, Nasser K., additional, Anand, Jatin, additional, Anderson, Robert H., additional, Anraku, Masaki, additional, Anyanwu, Anelechi C., additional, Arora, Amit, additional, Austin, Erle H., additional, Awtry, Eric H., additional, Bacha, Emile A., additional, Backhus, Leah M., additional, Bagai, Jayant, additional, Baillot, Richard, additional, Baird, Christopher W., additional, Barron, David J., additional, Bavaria, Joseph E., additional, Bernal, Jose M., additional, Bianco, Valentino J., additional, Bichell, David P., additional, Birgisson, Sigurbjorn, additional, Blackburn, Nick J.R., additional, Bonatti, Johannes, additional, Boodhwani, Munir, additional, Bove, Edward L., additional, Brawn, William J., additional, Brizard, Christian P., additional, Brothers, Julie A., additional, Brown, Lisa M., additional, Bryant, Ayesha S., additional, Burkhart, Harold M., additional, Caldarone, Christopher A., additional, Cannon, Jeremy W., additional, Carr, Justine M., additional, Castelvecchio, Serenella, additional, Castillo, Javier G., additional, Cecchin, Frank, additional, Cerfolio, Robert J., additional, Chahine, A. Alfred, additional, Chaikof, Elliot L., additional, Chan, Vincent, additional, Chaudhry, Sunit-Preet, additional, Chen, Frederick Y., additional, Chen, Stuart H., additional, Cheng, Aaron M., additional, Chien, Victor, additional, Chin, Alvin J., additional, Chin, Cynthia S., additional, Chiu, Peter, additional, Cleveland, Joseph C., additional, Cohn, Lawrence H., additional, Cohn, William E., additional, Colson, Yolonda L., additional, Colucci, Wilson S., additional, Cook, Andrew C., additional, Coselli, Joseph S., additional, Crawford, Todd C., additional, Culligan, Melissa, additional, Dagenais, François, additional, Damiano, Ralph J., additional, D'Amico, Thomas A., additional, Dartevelle, Philippe G., additional, David, Tirone E., additional, D'Cunha, Jonathan, additional, de la Cruz, Kim I., additional, Dearani, Joseph A., additional, DeArmond, Daniel T., additional, del Nido, Pedro J., additional, DeMeester, Tom R., additional, Demers, Philippe, additional, Demmy, Todd L., additional, Dexter, Elisabeth U., additional, Dhupar, Rajeev, additional, DiNardo, James A., additional, Doyle, Thomas P., additional, Ehsan, Afshin, additional, Khoury, Gebrine El, additional, Ellis, Ethan R., additional, Elmadhun, Nassrene Y., additional, Emani, Sitaram M., additional, Erasmus, Jeremy J., additional, Fauza, Dario O., additional, Fein, Adam S., additional, Fiedler, Amy G., additional, Foppa, Murilo, additional, Freeman, Rosario V., additional, Friedberg, Joseph, additional, Friscia, Michael, additional, Fynn-Thompson, Francis, additional, Gaynor, J. William, additional, Ge, Liang, additional, Geva, Tal, additional, Gheewala, Neil M., additional, Gillinov, A. Marc, additional, Glower, Donald D., additional, Goldstone, Andrew B., additional, Groth, Shawn S., additional, Grover, Frederick L., additional, Guccione, Julius, additional, Ha, Richard, additional, Hammon, John W., additional, Hanna, Jennifer M., additional, Harrison, David G., additional, Hauser, Thomas H., additional, Henn, Matthew C., additional, Hirsch-Romano, Jennifer C., additional, Hoang, Chuong D., additional, Hofstetter, Wayne L., additional, Honjo, Osami, additional, Huynh, Tam T., additional, Bravo, Carlos E., additional, Iturra, Sebastian, additional, Jacobs, Jeffrey P., additional, Jacobs, Marshall L., additional, Jaklitsch, Michael T., additional, Jamieson, Stuart W., additional, Jarrar, Doraid, additional, Jarrett, Craig M., additional, Jones, David R., additional, Josephson, Mark E., additional, Joventino, Lilian P., additional, Juraszek, Amy L., additional, Kachala, Stefan S., additional, Kaiser, Larry R., additional, Kanter, Kirk R., additional, Karamichalis, John M., additional, Kaza, Aditya K., additional, Kemp, Clinton D., additional, Kernstine, Kemp H., additional, Keshavamurthy, Suresh, additional, Keshavjee, Shaf, additional, Kozik, Deborah J., additional, Laham, Roger J., additional, Landzberg, Michael J., additional, Lawrance, Christopher P., additional, Lee, Lawrence S., additional, LeMaire, Scott A., additional, Levitsky, Sidney, additional, Levy, Jerrold H., additional, Linden, Philip A., additional, Liptay, Michael J., additional, Litle, Virginia R., additional, Rito, Mauro Lo, additional, Luketich, James D., additional, Lytle, Bruce W., additional, Madani, Michael, additional, Mahmood, Feroze, additional, Mallidi, Hari R., additional, Mangi, Abeel A., additional, Manning, Warren J., additional, Marom, Edith M., additional, Marshall, Audrey C., additional, Martinez, Mauricio Perez, additional, Mascio, Christopher E., additional, Mason, David P., additional, Mathisen, Douglas J., additional, Mattox, Kenneth L., additional, Matyal, Robina, additional, McCully, James D., additional, McKenna, Robert J., additional, McNamee, Ciaran, additional, McNeil, Jeffrey D., additional, Menicanti, Lorenzo, additional, Mestres, Carlos A., additional, Mettler, Bret A., additional, Meyers, Bryan Fitch, additional, Mick, Stephanie, additional, Mihaljevic, Tomislav, additional, Milano, Carmelo A., additional, Miller, D. Craig, additional, Miller, Daniel L., additional, Miller, Meagan M., additional, Mitchell, John D., additional, Montealegre-Gallegos, Mario, additional, Moores, Neal G., additional, Murphy, Charles E., additional, Murthy, Raghav A., additional, Murthy, Sudish C., additional, Mussot, Sacha, additional, Naka, Yoshifumi, additional, Nathan, Meena, additional, Newman, Kurt D., additional, Nwogu, Chukwumere, additional, Odegard, Kirsten C., additional, Oh, Daniel S., additional, Ohye, Richard G., additional, Onaitis, Mark W., additional, Ostojic, Aleksandra, additional, Ott, Harald C., additional, Ouzounian, Maral, additional, Owais, Khurram, additional, Padalino, Massimo, additional, Papadakis, Konstantinos, additional, Patterson, G.A., additional, Patz, Edward F., additional, Paul, Subroto, additional, Pennathur, Arjun, additional, Perry, Yaron, additional, Piana, Robert N., additional, Pigula, Frank A., additional, Pinto, Duane S., additional, Pomar, Jose L., additional, Preventza, Ourania, additional, Pua, Bradley, additional, Puri, Varun, additional, Quinonez, Luis, additional, Raja, Siva, additional, Ratcliffe, Mark, additional, Reardon, Michael J., additional, Reilly, John J., additional, Reyes, Karl G., additional, Rice, Thomas W., additional, Robbins, Robert C., additional, Rocco, Gaetano, additional, Rubens, Fraser D., additional, Ruel, Marc, additional, Rusch, Valerie W., additional, Sabe, Ashraf A., additional, Said, Sameh M., additional, Samson, Pamela P., additional, Sanders, Stephen P., additional, Sarin, Eric L., additional, Schaff, Hartzell V., additional, Schaheen, Lara W., additional, Seder, Christopher W., additional, Sellke, Frank W., additional, Sepesi, Boris, additional, Shahani, Rohit, additional, Shamberger, Robert C., additional, Shapira, Oz M., additional, Shay, Steven S., additional, Shrager, Joseph B., additional, Si, Ming-Sing, additional, Singh, Steve K., additional, Smith, Peter K., additional, Sodha, Neel R., additional, Solaro, R. John, additional, Soukiasian, Harmik J., additional, Spurlock, David, additional, Stellin, Giovanni, additional, Stiles, Brendon M., additional, Straznicka, Michaela, additional, Stump, David A., additional, Sugarbaker, David J., additional, Suuronen, Erik J., additional, Svensson, Lars G., additional, Swanson, Scott J., additional, Szeto, Wilson Y., additional, Taghavi, Sharven, additional, Takayama, Hiroo, additional, Takeda, Koji, additional, Thiagarajan, Ravi R., additional, Thistlethwaite, Patricia A., additional, Thourani, Vinod H., additional, Toeg, Hadi D., additional, Tong, Michael Z., additional, Truesdell, Alexander G., additional, Tsai, Peter I., additional, Urschel, Harold C., additional, Valente, Anne Marie, additional, Vallabhajosyula, Prashanth, additional, Velotta, Jeffrey B., additional, Vida, Vladimiro, additional, Vlahakes, Gus J., additional, Voisine, Pierre, additional, Wall, Matthew J., additional, Walsh, Garrett L., additional, Walters, Dustin M., additional, Wei, Benjamin, additional, Welsby, Ian J., additional, Westfall, Margaret V., additional, Wiener, Daniel C., additional, Wilcox, Benson R., additional, Williams, Judson B., additional, Wilson, Jay M., additional, Woo, Y. Joseph, additional, Wood, Douglas E., additional, Wylie, John V., additional, Yang, Stephen C., additional, Yendamuri, Sai, additional, Yeon, Susan B., additional, and Zimetbaum, Peter J., additional
- Published
- 2016
- Full Text
- View/download PDF
3. Transthoracic Fundoplication
- Author
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Pennathur, Arjun, primary and Luketich, James D., additional
- Published
- 2013
- Full Text
- View/download PDF
4. Contributors
- Author
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Albäck, Anders, primary, Ali, Mohamed, additional, Balaa, Fady K., additional, Beger, Hans G., additional, Belghiti, Jacques, additional, Bijelic, Lana, additional, Bismuth, Henri, additional, Blankensteijn, Jan D., additional, Briccoli, Antonio, additional, Buchwald, Henry, additional, Cadière, Guy Bernard, additional, Cahan, Mitchell A., additional, Campanacci, Laura, additional, Carlson, Grant W., additional, Cherqui, Daniel, additional, Ciancio, Gaetano, additional, Cima, Robert R., additional, Clark, Orlo H., additional, Coggia, Marc, additional, Crawford, Alvin H., additional, Dapri, Giovanni, additional, Darzi, Ara, additional, De Lorenzi, Francesca, additional, Decaluwe, Herbert, additional, Deeba, Samer S., additional, Delbridge, Leigh, additional, Ditto, Antonino, additional, Duh, Quan-Yang, additional, Eilber, Frederick R., additional, Eilber, Fritz C., additional, Elaraj, Dina M., additional, Errani, Costantino, additional, de Faria, José Carlos Marques, additional, Farmer, Diana, additional, Fernández-Cruz, Laureano, additional, Fransen, Philip, additional, Froix, Anthony J., additional, Fukagawa, Takeo, additional, Gagner, Michel, additional, Gauvin, Jeffrey M., additional, Geller, David A., additional, Gershenson, David M., additional, Gewertz, Bruce L., additional, Gigot, Jean-François, additional, Goëau-Brissonnière, Olivier, additional, Gokaslan, Ziya L., additional, Han, Ho-Seong, additional, Hanozet, Francesco, additional, Heald, Richard J., additional, Hemming, Alan W., additional, Henderson, J. Michael, additional, Hoekstra, Harald J.J., additional, Hsin, Michael K.Y., additional, Hubert, Catherine, additional, Ishiguro, Seiji, additional, Jakab, Ferenc, additional, Janetschek, Guenter, additional, Karin, Eliad, additional, Katkhouda, Namir, additional, Kavic, Stephen M., additional, Kemeny, M. Margaret, additional, Khatri, Vijay P., additional, Kitano, Seigo, additional, Klingler, H. Christoph, additional, Köckerling, Ferdinand, additional, Lee, Sang W., additional, Leo, Francesco, additional, Lepäntalo, Mauri, additional, Lerut, Toni, additional, Litwin, Demetrius E.M., additional, Lopes, Ademar, additional, Luketich, James D., additional, Lundgren, Catharina Ihre, additional, Lygidakis, N.J., additional, Mabrut, Jean-Yves, additional, Mahtabifard, Ali, additional, Makuuchi, Masatoshi, additional, Malawer, Martin M., additional, Marberger, Michael, additional, McKenna, Robert J., additional, Medina, Jesus E., additional, Mehran, Reza John, additional, Mekeel, Kristin L., additional, Mercuri, Mario, additional, Michelassi, Fabrizio, additional, Moesta, K. Thomas, additional, Moossa, A.R., additional, Moran, Brendan J., additional, Moriya, Yoshihiro, additional, Nagle, Alexander P., additional, Ng, Calvin S.H., additional, Parikh, Manish, additional, Park, Adrian E., additional, Pemberton, John H., additional, Pennathur, Arjun, additional, Peracchia, Alberto, additional, Petit, Jean Yves, additional, Poch, Bertram, additional, Pomeroy, Claire, additional, Popescu, Irinel, additional, Popovici, Zeno I., additional, Ramirez, Pedro T., additional, Raspagliesi, Francesco, additional, Roh, Mark S., additional, Rosati, Riccardo, additional, Rosato, Ernest L., additional, Roth, Jack A., additional, Sano, Keiji, additional, Sasako, Mitsuru, additional, Scatton, Olivier, additional, Scher, Richard L., additional, Schneebaum, Schlomo, additional, Schultze Kool, Leo J., additional, Shaha, Ashok R., additional, Sharma, Sandesh Kumar, additional, Shende, Manisha, additional, Shiraishi, Norio, additional, Sippel, Rebecca S., additional, Skinner, Donald G., additional, Sohn, Helen J., additional, Soloway, Mark S., additional, Soper, Nathaniel J., additional, Spaggiari, Lorenzo, additional, Stein, John P., additional, Stoppa, René, additional, Sugarbaker, Paul H., additional, Torzilli, Guido, additional, Tracey, Jacqueline Y., additional, Uehara, Keisuke, additional, Verhaeghe, Pierre, additional, Wobbes, Theo, additional, Wolf, Randall K., additional, Wolinsky, Jean-Paul, additional, Wong, Jason T., additional, Yan, Tristan D., additional, Yeo, Charles J., additional, Yim, Anthony P.C., additional, Zanon, Claudio, additional, Zarins, Christopher K., additional, and Zorron, Ricardo, additional
- Published
- 2013
- Full Text
- View/download PDF
5. Contributors
- Author
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Abbott, Brian G., primary, Adams, David H., additional, Aklog, Lishan, additional, Agnihotri, Arvind K., additional, Aquila Allen, Louise A., additional, Allen, Mark S., additional, Altorki, Nasser K., additional, Anderson, Robert H., additional, Anraku, Masaki, additional, Anyanwu, Anelechi C., additional, Ashiku, Simon K., additional, Austin, Erle H., additional, Awtry, Eric H., additional, Bacha, Emile A., additional, Baillott, Richard, additional, Baim, Donald S., additional, Balsam, Leora B., additional, Barner, Hendrick B., additional, Barron, David J., additional, Bavaria, Joseph E., additional, Bichell, David P., additional, Bove, Edward L., additional, Brawn, William J., additional, Brizard, Christian P., additional, Brothers, Julie A., additional, Brown, Morgan L., additional, Bryant, Ayesha S., additional, Burkhart, Harold M., additional, Caldarone, Christopher A., additional, Califf, Robert M., additional, Cantu, Edward, additional, Carr, Justine M., additional, Carrozza, Joseph P., additional, Cecchin, Frank, additional, Cerfolio, Robert J., additional, Chacko, Riya S., additional, Chahine, Alfred, additional, Chan, Vincent, additional, Chen, Frederick Y., additional, Chin, Alvin J., additional, Chin, Cynthia S., additional, Chikwe, Joanna, additional, Chitwood, W. Randolph, additional, Christian, Karla G., additional, Christie, Neil A., additional, Cleveland, Joseph C., additional, Cohn, Lawrence H., additional, Cohn, William E., additional, Colson, Yolanda L., additional, Colucci, Wilson S., additional, Cook, Andrew C., additional, Cooper, Joel D., additional, Copeland, Jack G., additional, Cowan, Scott, additional, Culligan, Melissa, additional, Dagenais, Francois, additional, Damiano, Ralph J., additional, D'Amico, Thomas A., additional, Daniel, Jonathan, additional, Dartevelle, Philippe G., additional, David, Tirone E., additional, D'Cunha, Jonathan, additional, Dearani, Joseph A., additional, DeArmond, Daniel T., additional, del Nido, Pedro J., additional, DeMeester, Tom R., additional, Demers, Philippe, additional, Demmy, Todd L., additional, Devaney, Eric J., additional, Dexter, Elisabeth U., additional, Di Donato, Marisa, additional, Ducko, Christopher T., additional, Duncan, Brian W., additional, Duran, Carlos M.G., additional, Edwards, Fred H., additional, Emani, Sitaram M., additional, Erasmus, Jeremy J., additional, Fauza, Dario O., additional, Fernandez, Felix G., additional, Fernando, Hiran C., additional, Filsoufi, Farzan, additional, Fischbein, Michael P., additional, Freeman, Rosario V., additional, Friedberg, Joseph, additional, Fullerton, David A., additional, Fynn-Thompson, Francis, additional, Garcia, Lawrence A., additional, Gaynor, J. William, additional, Geva, Tal, additional, Gilbert, Sébastien, additional, Gillinov, A. Marc, additional, Glower, Donald D., additional, Gopaldas, Raja R., additional, Grover, Frederick L., additional, Guccione, Julius, additional, Gutierrez, Constanza J., additional, Guyton, John R., additional, Hammon, John W., additional, Hammond, Zane T., additional, Hauser, Thomas H., additional, Hirsch, Jennifer C., additional, Hoang, Chuong D., additional, Honjo, Osami, additional, Horvath, Keith A., additional, Jacobs, Jeffrey Phillip, additional, Jacobs, Marshall L., additional, Jaklitsch, Michael T., additional, Jamieson, Stuart W., additional, Jarrar, Doraid, additional, Johnston, Douglas R., additional, Jones, David R., additional, Josephson, Mark E., additional, Joventino, Lilian P., additional, Juraszek, Amy L., additional, Kaiser, Larry R., additional, Kanter, Kirk R., additional, Kaza, Aditya K., additional, Keller, Steven M., additional, Kemp, Clinton D., additional, Kernstine, Kemp H., additional, Keshavjee, Shaf, additional, Krasna, Mark J., additional, Kucharczuk, John C., additional, Kypson, Alan P., additional, Laham, Roger J., additional, Landzberg, Michael J., additional, Laussen, Peter C., additional, Lee, Lawrence S., additional, LeMaire, Scott A., additional, Levitsky, Sidney, additional, Levy, Jerrold H., additional, Liddicoat, John R., additional, Lin, Peter H., additional, Linden, Philip A., additional, Lipham, John C., additional, Liptay, Michael J., additional, Litle, Virginia R., additional, Lytle, Bruce W., additional, Luketich, James D., additional, Madani, Michael M., additional, Maddaus, Michael A., additional, Mahmood, Feroze, additional, Mallidi, Hari R., additional, Mangi, Abeel A., additional, Manning, Warren, additional, Marom, Edith M., additional, Marshall, Audrey C., additional, Mascio, Christopher E., additional, Mason, David P., additional, Mathisen, Douglas J., additional, Mattox, Kenneth L., additional, Matyal, Robina, additional, Mayer, John E., additional, McCulley, James, additional, McElhinney, Doff, additional, McGee, Edwin C., additional, McGowan, Francis X., additional, McNamee, Ciaran, additional, Melby, Spencer J., additional, Menicanti, Lorenzo, additional, Meyers, Bryan F., additional, Milano, Carmelo A., additional, Craig Miller, D., additional, Miller, Daniel L., additional, Mitchell, John D., additional, Morgan, Jeffrey A., additional, Murthy, Sudish C., additional, Mussot, Sacha, additional, Nagji, Alykhan S., additional, Naka, Yoshifumi, additional, Newman, Kurt D., additional, Nwogu, Chukwumere, additional, Odegard, Kirsten C., additional, Ohye, Richard G., additional, Onaitis, Mark W., additional, Otto, Catherine M., additional, Oz, Mehmet C., additional, Park, Bernard J., additional, Patel, Amit N., additional, Alexander Patterson, G., additional, Patz, Edward F., additional, Paul, Subroto, additional, Pennathur, Arjun, additional, Pigula, Frank A., additional, Pinto, Duane S., additional, Pomerantz, Marvin, additional, Port, Jeffrey L., additional, Pride, Yuri B., additional, Puri, Varun, additional, Ramlawi, Basel, additional, Ratcliffe, Mark, additional, Reilly, John J., additional, Reitz, Bruce A., additional, Reyes, Karl G., additional, Rice, Thomas W., additional, Robbins, Robert C., additional, Rocco, Gaetano, additional, Rosinberg, Audrey, additional, Rubens, Fraser, additional, Ruel, Marc, additional, Rusch, Valerie W., additional, Sabik, Joseph F., additional, Schaff, Hartzell V., additional, Sellke, Frank W., additional, Shahani, Rohit, additional, Shamberger, Robert C., additional, Shay, Steven S., additional, Shrager, Joseph B., additional, Singhal, Dhruv, additional, Smith, Peter K., additional, Smith, Richard G., additional, Solaro, R. John, additional, Spurlock, David J., additional, Steiner, Marie E., additional, Steliga, Matthew A., additional, Stiles, Brendon M., additional, Straznicka, Michaela, additional, Stump, David A., additional, Sugarbaker, David J., additional, Suuronen, Erik J., additional, Svensson, Lars G., additional, Swanson, Scott J., additional, Szeto, Wilson Y., additional, Tanaka, Kenichi A., additional, Taylor, Benedict J.W., additional, Thistlethwaite, Patricia A., additional, Tsai, Peter, additional, Urschel, Harold C., additional, Valente, Anne Marie, additional, Van Natta, Timothy L., additional, Van Praagh, Richard, additional, Vasilyev, Nikolay V., additional, Velotta, Jeffrey B., additional, Vlahakes, Gus J., additional, Voisine, Pierre, additional, Wall, Matthew J., additional, Wallace, Arthur, additional, Walsh, Garrett L., additional, Weiner, Daniel C., additional, Weiser, Todd S., additional, Weksler, Benny, additional, Westfall, Margaret V., additional, Wilcox, Benson R., additional, Wilson, Jay M., additional, Wizorek, Joseph J., additional, Wood, Douglas E., additional, Wrobleskim, David, additional, Wylie, John V., additional, Yang, Stephen C., additional, Yankey, Godfred Kwame, additional, Yendamuri, Sai, additional, Yeon, Susan B., additional, Zaret, Barry L., additional, Zhang, Yan, additional, Zhao, Xiaoqin, additional, Zimetbaum, Peter J., additional, and Zimmerman, Hannah, additional
- Published
- 2010
- Full Text
- View/download PDF
6. Innovative Therapy and Technology
- Author
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Wizorek, Joseph J., primary, Pennathur, Arjun, additional, Christie, Neil A., additional, Fernando, Hiran C., additional, and Luketich, James D., additional
- Published
- 2010
- Full Text
- View/download PDF
7. EVALUATION AND SURGICAL TREATMENT OF HIATAL HERNIAS AND GASTROESOPHAGEAL REFLUX
- Author
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Irshad, Kashif, primary, Pennathur, Arjun, additional, and Luketich, James D., additional
- Published
- 2008
- Full Text
- View/download PDF
8. LAPAROSCOPIC TECHNIQUES IN REOPERATION FOR FAILED ANTIREFLUX REPAIRS
- Author
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Morse, Christopher R., primary, Pennathur, Arjun, additional, and Luketich, James D., additional
- Published
- 2008
- Full Text
- View/download PDF
9. Contributors
- Author
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Abbas, Ghulam, primary, Adelstein, David J., additional, Aigner, Clemens, additional, Alifano, Marco, additional, Allen, Mark S., additional, Altorki, Nasser K., additional, Andrade, Rafael S., additional, Andritsos, Michael J., additional, Arruda, M. Janine, additional, Ashiku, Simon K., additional, Ashrafi, Ahmad S., additional, Backer, Carl Lewis, additional, Bains, Majit S., additional, Baker, Mark E., additional, Banki, Farzaneh, additional, Bartlett, Nancy L., additional, Battafarano, Richard J., additional, Beauchamp, Gilles, additional, Bello, Ricardo A., additional, Bennett, W. Fred, additional, Bergeron, Michel G., additional, Bergeron, Yves, additional, Bhalla, Sanjeev, additional, Bizekis, Costas, additional, Boland, Brendan J., additional, Bousamra, Michael, additional, Bradley, Jeffrey D., additional, Brandolino, Mario, additional, Bredenberg, Carl E., additional, Bremner, Ross M., additional, Bronner, Mary P., additional, Bryant, Ayesha, additional, Burack, Joshua H., additional, Burgos, Raul, additional, Bussières, Jean S., additional, Campos, Javier H., additional, Cannie, Mieke, additional, Cassivi, Stephen D., additional, Casson, Alan G., additional, Castedo, Evaristo, additional, Cerfolio, Robert James, additional, Cetindag, Ibrahim Bulent, additional, Chelly, Jacques E., additional, Chiu, Priscilla, additional, Christie, Neil A., additional, Chung, Andy T.A., additional, Claytor, R. Brannon, additional, Cooper, Joel D., additional, Costantini, Mario, additional, Courcoulas, Anita P., additional, D'Amico, Thomas A., additional, Darling, Gail, additional, Dartevelle, Philippe, additional, de Hoyos, Alberto, additional, de Perrot, Marc, additional, De Wet, Charl J., additional, Debeer, Anne, additional, DeCamp, Malcolm M., additional, Dehdashti, Farrokh, additional, DeMeester, Steven R., additional, DeMeester, Tom R., additional, Deprest, Jan, additional, Deschamps, Claude, additional, Deslauriers, Jean, additional, Detterbeck, Frank C., additional, Díaz, Ismael A. Conti, additional, Doné, Elise, additional, Doody, Daniel P., additional, Downey, Gregory P., additional, Downey, Robert J., additional, Ducko, Christopher T., additional, Dumot, John A., additional, Duncan, Brian W., additional, Duranceau, André, additional, Edmundowicz, Steven A., additional, Einstein, David M., additional, Ellis, F. Henry, additional, Fadel, Elie, additional, Fell, Stanley C., additional, Fenske, Timothy S., additional, Ferguson, Mark K., additional, Fernandez, Felix G., additional, Fernando, Hiran C., additional, Ferraro, Pasquale, additional, Ferri, Lorenzo E., additional, Ferson, Peter F., additional, Finks, Jonathan F., additional, Finley, Richard J., additional, Flores, Raja M., additional, Fokin, Alexander A., additional, Fortin, Dalilah, additional, Fréchette, Éric, additional, Gaissert, Henning A., additional, Gamliel, Ziv, additional, Gandhi, Sanjiv K., additional, Ghefter, Mario C., additional, Gierada, David S., additional, Gilbert, Sebastien, additional, Goldstein, Allan M., additional, Govindan, Ramaswamy, additional, Graeber, Geoffrey M., additional, Grégoire, Jocelyn, additional, Griffin, Noreen, additional, Grillo, Hermes C., additional, Grunenwald, Dominique, additional, Gucciardo, Leonardo, additional, Gullane, Patrick J., additional, Hagen, Jeffrey A., additional, Lee Hall, Bruce, additional, Hantler, Charles, additional, Harpole, David H., additional, Harrison-Phipps, Karen, additional, Haughey, Bruce H., additional, Haustermans, Karin, additional, Hazelrigg, Stephen R., additional, Henschke, Claudia I., additional, Herridge, Margaret S., additional, Hiebert, Clement A., additional, Holinger, Lauren, additional, Hölscher, Arnulf H., additional, Hoover, Susan J., additional, Huang, Jasmine, additional, Huddleston, Charles B., additional, Hunter, John G., additional, Iannettoni, Mark D., additional, Ilson, David H., additional, Inculet, Richard I., additional, Irshad, Kashif, additional, Jacobsohn, Eric, additional, Jani, Jacques, additional, Javidan-Nejad, Cylen, additional, Jones, David R., additional, Jones, William G., additional, Jurkovich, Gregory, additional, Kaiser, Larry R., additional, Karmy-Jones, Riyad, additional, Keller, Steven M., additional, Kent, Michael S., additional, Keshavjee, Shaf, additional, Kesler, Kenneth A., additional, Klepetko, Walter, additional, Konstantakos, Anastasios, additional, Korst, Robert J., additional, Kozower, Benjamin D., additional, Krakovitz, Paul, additional, Krasna, Mark J., additional, Kreisel, Daniel, additional, Krishna, Priya D., additional, Krupnick, Alexander S., additional, Kucharczuk, John C., additional, Kwong, King F., additional, Landreneau, Rodney J., additional, Lang, Florian, additional, Langer, Jacob C., additional, Lara-Guerra, Humberto, additional, Lardinois, Didier, additional, Law, Simon, additional, Lefrak, Stephen S., additional, Leighl, Natasha B., additional, Leo, Francesco, additional, Lerut, Antoon (Toni) E.M.R., additional, Liebermann-Meffert, Dorothea, additional, Linden, Philip A., additional, Litle, Virginia R., additional, Little, Sherard, additional, Locadia, Mirjam, additional, Losso, Luis C., additional, Louie, Brian E., additional, Low, Donald E., additional, Luketich, James D., additional, Lundell, Lars, additional, Lutey, Barbara A., additional, Macchiarini, Paolo, additional, Mackinnon, Susan E., additional, Maddaus, Michael A., additional, Malthaner, Richard A., additional, Mason, David P., additional, Mathisen, Douglas J., additional, Mattioli, Sandro, additional, Mavroudis, Constantine, additional, Maziak, Donna E., additional, Mazur, Paul, additional, McLoud, Theresa, additional, McRae, Karen M., additional, Mehran, Reza John, additional, Mekhail, Tarek, additional, Merritt, Robert E., additional, Meyers, Bryan F., additional, Meyerson, Shari L., additional, Miller, Daniel L., additional, Miller, Joseph I., additional, Mineo, Tommaso C., additional, Minsky, Bruce D., additional, Moley, Jeffrey, additional, Monnier, Philippe, additional, Montano, Rachel, additional, Moreira, Andre L., additional, Morse, Christopher R., additional, Mouroux, Jérôme, additional, Müller, Nestor L., additional, Mulligan, Michael, additional, Murthy, Sudish C., additional, Naunheim, Keith, additional, Nelems, Bill, additional, Ng, Calvin S.H., additional, Nguyen, Ninh T., additional, Nichols, Francis C., additional, Novak, Christine B., additional, Odell, Michael J., additional, Ollyo, Jean-Baptiste, additional, Onaitis, Mark W., additional, Onders, Raymond P., additional, Ong, Sharon, additional, Orringer, Mark B., additional, Ouellette, Denise, additional, Pairolero, Peter C., additional, Papsin, Blake C., additional, Park, Bernard J., additional, Parsons, Alden M., additional, Partrick, David A., additional, Pasche, Philippe, additional, Pastorino, Ugo, additional, Patel, Amit N., additional, Patterson, G. Alexander, additional, Pearson, F. Griffith, additional, Peitzman, Andrew B., additional, Pennathur, Arjun, additional, Pera, Manuel, additional, Peracchia, Alberto, additional, Pereira, Sérgio Tadeu L.F., additional, Peters, Jeffrey H., additional, Pettiford, Brian, additional, Phillips, Kacy, additional, Pierre, Andrew F., additional, Pompeo, Eugenio, additional, Pop, Daniel, additional, Poylin, Vitaliy, additional, Propst, Evan J., additional, Putnam, Joe B., additional, Qadeer, Mohammed A., additional, Raghu, Ganesh, additional, Rayyan, Maissa, additional, Razzuk, Linda M., additional, Razzuk, Maruf A., additional, Rendina, Erino A., additional, Rice, Thomas W., additional, Richter, Joel E., additional, Ritter, Jon H., additional, Rizk, Nabil P., additional, Robicsek, Francis, additional, Rocco, Gaetano, additional, Rosati, Riccardo, additional, Rosen, Clark A., additional, Rusch, Valerie W., additional, Salzman, Steve H., additional, Sampliner, Richard E., additional, Savary, Marcel, additional, Sbragia, Lourenço, additional, Schipper, Paul H., additional, Schrump, David S., additional, Sciurba, Frank C., additional, Shepherd, Frances A., additional, Shrager, Joseph B., additional, Siegel, Barry A., additional, Sihoe, Alan D.L., additional, Singhal, Sunil, additional, Slinger, Peter D., additional, Smith, Philip W., additional, Soper, Nathaniel J., additional, Souza, Carolina A., additional, Sprangers, Mirjam A.G., additional, Stewart, Robert D., additional, Stroobants, Sigrid G., additional, Sugarbaker, David J., additional, Sullivan, Erin A., additional, Sundaresan, Sudhir R., additional, Swanström, Lee L., additional, Temes, R. Thomas, additional, Tronc, François, additional, Ugalde, Paula A., additional, Urschel, Harold C., additional, Vaezi, Michael F., additional, Vallières, Eric, additional, van Berge Henegouwen, Mark I., additional, Van de Velde, Marc, additional, van Lanschot, Jan J.B., additional, Van Mieghem, Tim, additional, Van Natta, Timothy L., additional, Van Schoubroeck, Dominique, additional, Varela, Andrés, additional, Veeramachaneni, Nirmal K., additional, Venissac, Nicolas, additional, Venuta, Federico, additional, Videtic, Gregory M.M., additional, Vivó, Jorge Nin, additional, Waddell, Thomas K., additional, Walsh, Garrett L., additional, Warren, William H., additional, Waters, Paul F., additional, Watson, Thomas J., additional, Watts, Larry T., additional, Weder, Walter, additional, Wick, Mark R., additional, Wigle, Dennis A., additional, Wildes, Troy S., additional, Wilkins, Earl Wayne, additional, Withers, H. Rodney, additional, Witterick, Ian, additional, Wizorek, Joseph J., additional, Wong, John, additional, Wood, Douglas E., additional, Wright, Cameron D., additional, Wrightson, William, additional, Ximenes-Netto, Manoel, additional, Yang, Steve, additional, Yankelevitz, David F., additional, Yazbeck, Salam, additional, Yim, Anthony P.C., additional, Zakowski, Maureen, additional, and Zuccaro, Gregory, additional
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- 2008
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10. A Pan-cancer analysis reveals high-frequency genetic alterations in mediators of signaling by the tgf-β superfamily
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Korkut, Anil, Zaidi, Sobia, Kanchi, Rupa S., Rao, Shuyun, Gough, Nancy R., Schultz, Andre, Li, Xubin, Lorenzi, Philip L., Berger, Ashton C., Robertson, Gordon, Kwong, Lawrence N., Datto, Mike, Roszik, Jason, Ling, Shiyun, Ravikumar, Visweswaran, Manyam, Ganiraju, Rao, Arvind, Shelley, Simon, Liu, Yuexin, Ju, Zhenlin, Hansel, Donna, Velasco, Guillermo de, Pennathur, Arjun, Andersen, Jesper B., O'Rourke, Colm J., Ohshiro, Kazufumi, Jogunoori, Wilma, Nguyen, Bao-Ngoc, Li, Shulin, Osmanbeyoglu, Hatice U., Ajani, Jaffer A., Mani, Sendurai A., Houseman, Andres, Wiznerowicz, Maciej, Chen, Jian, Gu, Shoujun, Ma, Wencai, Zhang, Jiexin, Tong, Pan, and Cancer Genome Atlas Research Network
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Cellular signal transduction ,Mutació (Biologia) ,Genetics ,Transducció de senyal cel·lular ,Mutation (Biology) ,Càncer ,Growth factors ,Genètica ,Factors de creixement ,Cancer - Abstract
We present an integromic analysis of gene alterations that modulate transforming growth factor β (TGF-β)-Smad-mediated signaling in 9,125 tumor samples across 33 cancer types in The Cancer Genome Atlas (TCGA). Focusing on genes that encode mediators and regulators of TGF-β signaling, we found at least one genomic alteration (mutation, homozygous deletion, or amplification) in 39% of samples, with highest frequencies in gastrointestinal cancers. We identified mutation hotspots in genes that encode TGF-β ligands (BMP5), receptors (TGFBR2, AVCR2A, and BMPR2), and Smads (SMAD2 and SMAD4). Alterations in the TGF-β superfamily correlated positively with expression of metastasis-associated genes and with decreased survival. Correlation analyses showed the contributions of mutation, amplification, deletion, DNA methylation, and miRNA expression to transcriptional activity of TGF-β signaling in each cancer type. This study provides a broad molecular perspective relevant for future functional and therapeutic studies of the diverse cancer pathways mediated by the TGF-β superfamily.
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- 2018
11. Management of Recurrent Paraesophageal Hernia.
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Witek TD, Luketich JD, Pennathur A, and Awais O
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- Humans, Laparoscopy, Patient Satisfaction, Recurrence, Treatment Outcome, Hernia, Hiatal surgery, Herniorrhaphy methods, Reoperation methods
- Abstract
Recurrent symptomatic paraesophageal hernias (PEHs) can lead to significant morbidity if untreated. Surgical treatment of recurrent PEH can pose a great challenge. Several different surgical options are available and need to be considered on an individual basis. Before embarking on the repair of a recurrent hernia, a thorough work-up needs to be completed. Although recurrent PEHs have traditionally been repaired through an open approach, a minimally invasive approach can be performed by surgeons with extensive experience in minimally invasive esophageal surgery. Repair of recurrent PEH provides excellent patient satisfaction and symptoms resolution. Routine follow-up with surveillance imaging can assist in treating recurrent symptoms., (Copyright © 2019 Elsevier Inc. All rights reserved.)
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- 2019
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12. Detection of Circulating Tumor DNA in Plasma: A Potential Biomarker for Esophageal Adenocarcinoma.
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Egyud M, Tejani M, Pennathur A, Luketich J, Sridhar P, Yamada E, Ståhlberg A, Filges S, Krzyzanowski P, Jackson J, Kalatskaya I, Jiao W, Nielsen G, Zhou Z, Litle V, Stein L, and Godfrey T
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- Adenocarcinoma blood, Adenocarcinoma genetics, Biomarkers, Tumor blood, Biomarkers, Tumor genetics, Circulating Tumor DNA blood, Disease Progression, Esophageal Neoplasms blood, Esophageal Neoplasms genetics, Female, Humans, Liquid Biopsy, Male, Adenocarcinoma diagnosis, Circulating Tumor DNA genetics, DNA, Neoplasm genetics, Esophageal Neoplasms diagnosis, Mutation, Neoplasm Staging methods
- Abstract
Background: Recent literature has demonstrated the potential of "liquid biopsy" and detection of circulating tumor (ct)DNA as a cancer biomarker. However, to date there is a lack of data specific to esophageal adenocarcinoma (EAC). This study was conducted to determine how detection and quantification of ctDNA changes with disease burden in patients with EAC and evaluate its potential as a biomarker in this population., Methods: Blood samples were obtained from patients with stage I to IV EAC. Longitudinal blood samples were collected from a subset of patients. Imaging studies and pathology reports were reviewed to determine disease course. Tumor samples were sequenced to identify mutations. Mutations in plasma DNA were detected using custom, barcoded, patient-specific sequencing libraries. Mutations in plasma were quantified, and associations with disease stage and response to therapy were explored., Results: Plasma samples from a final cohort of 38 patients were evaluated. Baseline plasma samples were ctDNA positive for 18 patients (47%) overall, with tumor allele frequencies ranging from 0.05% to 5.30%. Detection frequency of ctDNA and quantity of ctDNA increased with stage. Data from longitudinal samples indicate that ctDNA levels correlate with and precede evidence of response to therapy or recurrence., Conclusions: ctDNA can be detected in plasma of EAC patients and correlates with disease burden. Detection of ctDNA in early-stage EAC is challenging and may limit diagnostic applications. However, our data demonstrate the potential of ctDNA as a dynamic biomarker to monitor treatment response and disease recurrence in patients with EAC., (Copyright © 2019 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
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- 2019
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13. The Mesenchymal State Predicts Poor Disease-Free Survival in Resectable Non-Small Cell Lung Cancer.
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Mehta K, Moravcikova E, McFall D, Luketich JD, Pennathur A, Donnenberg AD, and Donnenberg VS
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- Adult, Aged, Aged, 80 and over, Carcinoma, Non-Small-Cell Lung mortality, Carcinoma, Non-Small-Cell Lung surgery, Disease-Free Survival, Female, Flow Cytometry, Humans, Lung Neoplasms mortality, Lung Neoplasms surgery, Male, Middle Aged, Prognosis, Survival Rate trends, United States epidemiology, Carcinoma, Non-Small-Cell Lung pathology, Epithelial-Mesenchymal Transition, Lung Neoplasms pathology, Neoplastic Stem Cells pathology, Pneumonectomy
- Abstract
Background: The epithelial-mesenchymal transition (EMT) is thought to contribute to the overall invasiveness of malignant cells. Expression of cluster of differentiation (CD) 44 and CD90 mark the mesenchymal state in multiple epithelial malignancies. Their role in lung cancer remains unclear, however. This study evaluated the prognostic significance of CD44 and CD90 coexpression in patients with resectable primary non-small cell lung cancer (NSCLC)., Methods: This was a nonconcurrent cohort study of patients with resectable NSCLC, stratified by the degree of expression of CD44/CD90 double-positive cells in their primary tumor. Flow cytometry was used for immunophenotyping of freshly isolated disaggregated tumor. We analyzed the relationship between expression of CD44/CD90 and relapse-free survival., Results: We evaluated 37 patients (18 men; median age, 70 years) with NSCLC. For this group, the geometric mean proportion of cells coexpressing CD44/CD90 was 0.52%. Expression of CD44/CD90 was significantly elevated (24.4%, geometric mean) in 6 patients. The median relapse-free survival for patients with high CD44/CD90 coexpression was 7.7 months (95% confidence interval, 4.2 to 11.7) compared with 40 months (95% confidence interval, 18.2 to 77.8) for the group with low CD44/CD90 coexpression (p = 0.00006 by Mantel log-rank test). The assessment of risk based upon CD44/CD90 expression status was not correlated with pathologic staging (p = 0.073 by χ
2 )., Conclusions: High expression of CD44 and CD90 was associated with significantly reduced relapse-free survival in NSCLC patients. These results suggest that CD44 and CD90 may be important markers of tumor progression in NSCLC., (Copyright © 2017 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)- Published
- 2017
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14. Targeting Immune Checkpoints in Esophageal Cancer: A High Mutational Load Tumor.
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Dhupar R, Van Der Kraak L, Pennathur A, Schuchert MJ, Nason KS, Luketich JD, and Lotze MT
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- B7-H1 Antigen metabolism, Biomarkers metabolism, CTLA-4 Antigen metabolism, Esophageal Neoplasms etiology, Humans, Programmed Cell Death 1 Receptor metabolism, Tumor Burden, Esophageal Neoplasms metabolism, Esophageal Neoplasms pathology
- Abstract
Checkpoint inhibitors (eg, programmed cell death protein 1 [PD-1], programmed cell death ligand 1 [PD-L1], cytotoxic T-lymphocyte associated protein 4 [CTLA-4] antibodies) are changing how we understand cancer and provide a means to develop modern immunotherapies. An emergent notion relates success with checkpoint inhibitors with high mutational load tumors. There are few studies that examine checkpoint protein expression and relate these to clinical outcomes after the conventional treatment of patients with esophageal cancer, which has a high mutational load. The objective of this review is to summarize the literature that examines checkpoint expression and clinical outcomes, as well as propose an accelerated approach to introducing these therapies into the clinic to treat patients with esophageal cancer., (Copyright © 2017 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
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- 2017
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15. Reply.
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Macke RA, Luketich JD, Pennathur A, and Levy RM
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- 2016
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16. Electromagnetic Navigation Bronchoscopy-Guided Dye Marking for Thoracoscopic Resection of Pulmonary Nodules.
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Awais O, Reidy MR, Mehta K, Bianco V, Gooding WE, Schuchert MJ, Luketich JD, and Pennathur A
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- Aged, Electromagnetic Phenomena, Female, Humans, Lung Neoplasms surgery, Male, Multiple Pulmonary Nodules surgery, Retrospective Studies, Tomography, X-Ray Computed, Bronchoscopy methods, Early Detection of Cancer, Lung Neoplasms diagnosis, Multiple Pulmonary Nodules diagnosis, Pneumonectomy methods, Thoracoscopy methods
- Abstract
Background: Computed tomography scans are increasingly used not only for lung cancer screening but also for staging and evaluation of other cancers. As a result, more patients with pulmonary nodules, many with subcentimeter lesions, are being referred to thoracic surgeons, some with concern for primary lung neoplasm and others with possible metastatic lung lesions. Obtaining a definitive diagnosis of these lesions is difficult. Electromagnetic navigational bronchoscopy (ENB)-guided pleural dye marking followed by thoracoscopic resection is a novel alternative technique for definitive diagnosis. The main objective of this study was to evaluate the feasibility and our initial experience with ENB-guided dye localization and minimally invasive resection for diagnosis of lung lesions., Methods: Selected patients with lung lesions underwent ENB-guided dye marking and minimally invasive resection. The primary end points were the rate of nodule localization and definitive diagnosis of the nodule., Results: We performed ENB-guided localization and minimally invasive resection in 29 patients. The median lesion size was 10 mm, with a median distance from pleural surface of 13 mm. The operative mortality was 0%. The median hospital stay was 3 days. The nodule was localized and resected, and a definitive diagnosis was obtained in all patients (29 of 29; 100%). The nodule was neoplastic in 19 patients. All malignant lesions were completely resected with negative microscopic margins., Conclusions: Our initial experience with ENB-guided dye localization and minimally invasive resection found that the technique was feasible, safe, and successful in the diagnosis of small lung lesions. Thoracic surgeons should further investigate this method and incorporate it into their armamentarium., (Copyright © 2016 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
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- 2016
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17. Multiplex Preamplification of Serum DNA to Facilitate Reliable Detection of Extremely Rare Cancer Mutations in Circulating DNA by Digital PCR.
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Jackson JB, Choi DS, Luketich JD, Pennathur A, Ståhlberg A, and Godfrey TE
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- DNA, Neoplasm genetics, DNA-Directed DNA Polymerase genetics, DNA-Directed DNA Polymerase metabolism, Gene Frequency, Humans, Polymerase Chain Reaction methods, Proto-Oncogene Proteins p21(ras) genetics, Sensitivity and Specificity, Smad4 Protein genetics, Tumor Suppressor Protein p53 genetics, DNA Mutational Analysis methods, DNA, Neoplasm blood, Neoplasms genetics, Nucleic Acid Amplification Techniques methods
- Abstract
Tumor-specific mutations can be identified in circulating, cell-free DNA in plasma or serum and may serve as a clinically relevant alternative to biopsy. Detection of tumor-specific mutations in the plasma, however, is technically challenging. First, mutant allele fractions are typically low in a large background of wild-type circulating, cell-free DNA. Second, the amount of circulating, cell-free DNA acquired from plasma is also low. Even when using digital PCR (dPCR), rare mutation detection is challenging because there is not enough circulating, cell-free DNA to run technical replicates and assay or instrument noise does not easily allow for mutation detection <0.1%. This study was undertaken to improve on the robustness of dPCR for mutation detection. A multiplexed, preamplification step using a high-fidelity polymerase before dPCR was developed to increase total DNA and the number of targets and technical replicates that can be assayed from a single sample. We were able to detect multiple cancer-relevant mutations within tumor-derived samples down to 0.01%. Importantly, the signal/noise ratio was improved for all preamplified targets, allowing for easier discrimination of low-abundance mutations against false-positive signal. Furthermore, we used this protocol on clinical samples to detect known, tumor-specific mutations in patient sera. This study provides a protocol for robust, sensitive detection of circulating tumor DNA for future clinical applications., (Copyright © 2016 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. All rights reserved.)
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- 2016
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18. Stereotactic Radiosurgery/Stereotactic Body Radiotherapy for Recurrent Lung Neoplasm: An Analysis of Outcomes in 100 Patients.
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Pennathur A, Luketich JD, Heron DE, Schuchert MJ, Bianco V, Clump D, Burton S, Abbas G, Gooding WE, Ozhasoglu C, Landreneau RJ, and Christie NA
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- Adult, Aged, Aged, 80 and over, Disease Progression, Dose-Response Relationship, Radiation, Female, Follow-Up Studies, Humans, Lung Neoplasms mortality, Male, Middle Aged, Neoplasm Recurrence, Local mortality, Pennsylvania epidemiology, Retrospective Studies, Survival Rate trends, Time Factors, Treatment Outcome, Lung Neoplasms surgery, Neoplasm Recurrence, Local surgery, Radiosurgery methods
- Abstract
Background: A significant number of patients have recurrent or persistent lung cancer despite complete resection or treatment with definitive chemoradiation. Stereotactic radiosurgery (SRS)/stereotactic body radiation therapy is emerging as an important modality for the treatment of early-stage lung neoplasm; SRS may also offer an alternative treatment option for patients with recurrent lung disease. We evaluated outcomes after treatment with SRS for recurrent lung neoplasm in a large series of patients., Methods: Selected patients with limited recurrent, persistent, or progressive disease after one or more prior treatments for lung cancer were offered SRS. Thoracic surgeons evaluated all patients, placed fiducials when needed, and planned treatment in close collaboration with radiation oncologists and medical physicists. In our early experience, a single fraction of 20 Gy radiation was prescribed and was subsequently increased to 45 to 60 Gy in three to five fractions. The primary endpoint evaluated was overall survival., Results: We treated 100 patients with recurrent lung cancer (median age 72 years) with SRS. The postprocedure 30-day mortality rate was 0%; median follow-up was 51 months (range, 5 to 123). The median overall survival for the entire group was 23 months (95% confidence interval: 19 to 41). The probability of 2-year and 5-year overall survival was 49% (95% confidence interval: 40% to 60%) and 31% (95% confidence interval: 23% to 43%), respectively., Conclusions: Our experience indicates that SRS is safe, and offers an alternative modality for selected patients with recurrent oligometastatic or persistent lung cancer. Thoracic surgeons should actively participate in SRS and continue to evaluate the efficacy of this treatment strategy., (Copyright © 2015 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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19. Lung Cancer Risk Prediction Using Common SNPs Located in GWAS-Identified Susceptibility Regions.
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Weissfeld JL, Lin Y, Lin HM, Kurland BF, Wilson DO, Fuhrman CR, Pennathur A, Romkes M, Nukui T, Yuan JM, Siegfried JM, and Diergaarde B
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- Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Risk Factors, Genome-Wide Association Study methods, Lung Neoplasms genetics, Polymorphism, Single Nucleotide genetics
- Abstract
Introduction: Genome-wide association studies (GWAS) have consistently identified specific lung cancer susceptibility regions. We evaluated the lung cancer-predictive performance of single-nucleotide polymorphisms (SNPs) in these regions., Methods: Lung cancer cases (N = 778) and controls (N = 1166) were genotyped for 77 SNPs located in GWAS-identified lung cancer susceptibility regions. Variable selection and model development used stepwise logistic regression and decision-tree analyses. In a subset nested in the Pittsburgh Lung Screening Study, change in area under the receiver operator characteristic curve and net reclassification improvement were used to compare predictions made by risk factor models with and without genetic variables., Results: Variable selection and model development kept two SNPs in each of three GWAS regions, rs2736100 and rs7727912 in 5p15.33, rs805297 and rs1802127 in 6p21.33, and rs8034191 and rs12440014 in 15q25.1. The ratio of cases to controls was three times higher among subjects with a high-risk genotype in every one as opposed to none of the three GWAS regions (odds ratio, 3.14; 95% confidence interval, 2.02-4.88; adjusted for sex, age, and pack-years). Adding a three-level classified count of GWAS regions with high-risk genotypes to an age and smoking risk factor-only model improved lung cancer prediction by a small amount: area under the receiver operator characteristic curve, 0.725 versus 0.717 (p = 0.056); overall net reclassification improvement was 0.052 across low-, intermediate-, and high- 6-year lung cancer risk categories (<3.0%, 3.0%-4.9%, ≥ 5.0%)., Conclusion: Specifying genotypes for SNPs in three GWAS-identified susceptibility regions improved lung cancer prediction, but probably by an extent too small to affect disease control practice.
- Published
- 2015
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20. Thoracic Esophageal Diverticula: A 15-Year Experience of Minimally Invasive Surgical Management.
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Macke RA, Luketich JD, Pennathur A, Bianco V, Awais O, Gooding WE, Christie NA, Schuchert MJ, Nason KS, and Levy RM
- Subjects
- Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Retrospective Studies, Thorax, Time Factors, Treatment Outcome, Diverticulum, Esophageal surgery, Laparoscopy, Thoracic Surgery, Video-Assisted
- Abstract
Background: Thoracic esophageal diverticula are uncommon, and controversies exist regarding their management. The objective of this study was to evaluate the outcomes of a relatively large cohort of patients with thoracic esophageal diverticula treated with minimally invasive surgical techniques., Methods: We conducted a retrospective review of patients who underwent minimally invasive surgical treatment for symptomatic esophageal diverticula during a 15-year period. The primary end point was 30-day mortality. In addition, we evaluated the morbidity, improvement in dysphagia (score: 1, best to 5, worst), and quality of life (Gastroesophageal Reflux Disease-Health-Related Quality of Life score: 0, best to 50, most symptoms)., Results: Fifty-seven patients underwent minimally invasive surgical treatment of symptomatic thoracic esophageal diverticula. The most common symptom was dysphagia (45 of 57; 79%). A motility disorder or distal mechanical obstruction was identified in 49 patients (86%). Approaches used included video-assisted thoracoscopic surgery (n = 33), laparoscopy (n = 18), and combined video-assisted thoracoscopic surgery and laparoscopy (n = 6). The most common procedure performed was diverticulectomy and myotomy (47 of 57 patients; 82.5%). The 30-day mortality was 0%. There were 4 patients (7%) with postoperative leaks requiring reoperation. During follow-up, the median dysphagia score improved from 3 to 1 (p < 0.001). The median Gastroesophageal Reflux Disease-Health-Related Quality of Life score after surgery was 5 (excellent)., Conclusions: A minimally invasive surgical approach for the management of thoracic esophageal diverticula is safe and effective during intermediate-term follow-up when performed by surgeons experienced in esophageal surgery and minimally invasive techniques. Further follow-up is required to assess the durability of these results. The optimal approach and procedures performed should be determined on an individualized basis after a thorough investigation., (Copyright © 2015 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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21. Expression of PAM50 Genes in Lung Cancer: Evidence that Interactions between Hormone Receptors and HER2/HER3 Contribute to Poor Outcome.
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Siegfried JM, Lin Y, Diergaarde B, Lin HM, Dacic S, Pennathur A, Weissfeld JL, Romkes M, Nukui T, and Stabile LP
- Subjects
- Aged, Carcinoma, Non-Small-Cell Lung genetics, Carcinoma, Non-Small-Cell Lung mortality, Cohort Studies, Estrogen Receptor beta genetics, Female, Humans, Lung Neoplasms genetics, Lung Neoplasms mortality, Male, Middle Aged, Protein Binding physiology, Receptor, ErbB-2 genetics, Receptor, ErbB-3 genetics, Survival Rate trends, Tissue Array Analysis trends, Treatment Outcome, Carcinoma, Non-Small-Cell Lung metabolism, Estrogen Receptor beta biosynthesis, Gene Expression Regulation, Neoplastic, Lung Neoplasms metabolism, Receptor, ErbB-2 biosynthesis, Receptor, ErbB-3 biosynthesis
- Abstract
Non-small cell lung cancers (NSCLCs) frequently express estrogen receptor (ER) β, and estrogen signaling is active in many lung tumors. We investigated the ability of genes contained in the prediction analysis of microarray 50 (PAM50) breast cancer risk predictor gene signature to provide prognostic information in NSCLC. Supervised principal component analysis of mRNA expression data was used to evaluate the ability of the PAM50 panel to provide prognostic information in a stage I NSCLC cohort, in an all-stage NSCLC cohort, and in The Cancer Genome Atlas data. Immunohistochemistry was used to determine status of ERβ and other proteins in lung tumor tissue. Associations with prognosis were observed in the stage I cohort. Cross-validation identified seven genes that, when analyzed together, consistently showed survival associations. In pathway analysis, the seven-gene panel described one network containing the ER and progesterone receptor, as well as human epidermal growth factor receptor (HER)2/HER3 and neuregulin-1. NSCLC cases also showed a significant association between ERβ and HER2 protein expression. Cases positive for HER2 expression were more likely to express HER3, and ERβ-positive cases were less likely to be both HER2 and HER3 negative. Prognostic ability of genes in the PAM50 panel was verified in an ERβ-positive cohort representing all NSCLC stages. In The Cancer Genome Atlas data sets, the PAM50 gene set was prognostic in both adenocarcinoma and squamous cell carcinoma, whereas the seven-gene panel was prognostic only in squamous cell carcinoma. Genes in the PAM50 panel, including those linking ER and HER2, identify lung cancer patients at risk for poor outcome, especially among ERβ-positive cases and squamous cell carcinoma., (Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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22. Roux-en-Y near esophagojejunostomy for failed antireflux operations: outcomes in more than 100 patients.
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Awais O, Luketich JD, Reddy N, Bianco V, Levy RM, Schuchert MJ, Gooding WE, Crist LR, Landreneau RJ, and Pennathur A
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- Adult, Aged, Aged, 80 and over, Female, Follow-Up Studies, Forecasting, Gastroesophageal Reflux psychology, Humans, Length of Stay trends, Male, Middle Aged, Patient Satisfaction, Quality of Life psychology, Reoperation, Retrospective Studies, Treatment Failure, Treatment Outcome, Young Adult, Anastomosis, Roux-en-Y methods, Esophagus surgery, Gastroesophageal Reflux surgery, Jejunostomy methods, Jejunum surgery, Laparoscopy methods
- Abstract
Background: Intractable gastroesophageal reflux disease (GERD) after antireflux operations presents a challenge-particularly in obese patients and patients with esophageal dysmotility-and increases the complexity of the redo operation. This study evaluated the results of Roux-en-Y near esophagojejunostomy (RNYNEJ) in the management of recurrent GERD after antireflux operations., Methods: We conducted a retrospective review of overweight patients with intractable GERD who underwent RNYNEJ for failed antireflux operations. We evaluated perioperative outcomes, dysphagia (ranging from 1 = no dysphagia to 5 = unable to swallow saliva), and quality of life (QOL) (assessed using the GERD health-related quality-of-life instrument (HRQOL)., Results: Over a 12-year period, 105 patients with body mass index (BMI) greater than 25 underwent RNYNEJ for failed antireflux operations. Most were obese (BMI > 30; 82 patients [78%]); esophageal dysmotility was demonstrated in more than one-third of patients. Forty-eight (46%) patients had multiple antireflux operations before RNYNEJ, and 27 patients had undergone a previous Collis gastroplasty. There was no perioperative mortality. Major complications, including anastomotic leak requiring surgical intervention (n = 3 [2.9%]), were noted in 25 patients (24%).The median length of stay was 6 days. During follow-up (mean, 23.39 months), median BMI decreased from 35 to 27.6 (p < 0.0001), and the mean dysphagia score decreased from 2.9 to 1.5 (p < 0.0001). The median GERD HRQOL score, assessed in a subset of patients, was 9 (classified as excellent)., Conclusions: RNYNEJ for persistent GERD after antireflux operations in appropriately selected patients can be performed safely with good results in experienced centers. RNYNEJ should be considered an important option for the treatment of intractable recurrent symptoms after antireflux operations, particularly in obese patients., (Copyright © 2014 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2014
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23. Inherited variation in the ATP-binding cassette transporter ABCB1 and survival after chemotherapy for stage III-IV lung cancer.
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Weissfeld JL, Diergaarde B, Nukui T, Buch S, Pennathur A, Socinski MA, Siegfried JM, and Romkes M
- Subjects
- ATP Binding Cassette Transporter, Subfamily B genetics, ATP Binding Cassette Transporter, Subfamily B metabolism, Aged, Aged, 80 and over, Alleles, Carcinoma, Non-Small-Cell Lung diagnosis, Carcinoma, Non-Small-Cell Lung drug therapy, Female, Follow-Up Studies, Genetic Predisposition to Disease, Genotype, Humans, Lung Neoplasms drug therapy, Lung Neoplasms mortality, Male, Middle Aged, Pennsylvania epidemiology, Retrospective Studies, Survival Rate trends, Antineoplastic Agents therapeutic use, Carcinoma, Non-Small-Cell Lung genetics, DNA, Neoplasm genetics, Lung Neoplasms genetics, Neoplasm Staging, Polymorphism, Genetic
- Abstract
Background: The ATP-binding cassette transporter gene ABCB1 and the glutathione S-transferase gene GSTP1 code for a multidrug resistance protein and for a detoxifying phase II metabolic enzyme, respectively, with substrate specificities that include chemotherapy drugs often used to treat lung cancer., Methods: We genotyped 11 ABCB1 and eight GSTP1 single nucleotide polymorphisms (SNPs) in 698 white lung cancer patients (all current or former cigarette smokers) and used log-rank test statistics and proportional hazards regression to evaluate associations between SNP genotype and survival., Results: Using data from all 698 cases, one SNP in ABCB1 (rs2235013) was statistically significantly associated with overall survival (p = 0.038, log-rank test). Chemotherapy and stage jointly (p = 0.025) significantly modified the association between rs2235013 and survival, with statistically significant (p = 0.013, log-rank test) association observed in the subgroup of stage III to IV lung cancer patients who received chemotherapy as part of their first course of treatment (n = 160; 93.1% nonsmall cell). Patients who inherited the minor T allele at ABCB1 rs2235013 experienced better overall survival and recurrence-free survival (hazard ratio, per minor T allele, [95% confidence interval]: 0.66 [0.49-0.90] and 0.55 [0.31-0.95], respectively; adjusted for year of diagnosis, sex, age at diagnosis, cigarette pack years, and stage). In addition, in the advanced stage chemotherapy-treated subgroup, four ABCB1 SNPs (rs6949448, rs2235046, rs1128503, and rs10276036) in mutual high linkage disequilibrium with rs2235013 and an independent ABCB1 SNP (rs1045642) showed statistically significant association (p < 0.05) with survival., Conclusions: Inherited variation in ABCB1 may affect survival specifically in advanced stage lung cancer patients who receive chemotherapy.
- Published
- 2014
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24. Anterior thoracic surgical approaches in the treatment of spinal infections and neoplasms.
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Schuchert MJ, McCormick KN, Abbas G, Pennathur A, Landreneau JP, Landreneau JR, Pitanga A, Gomes J, Franca F, El-Kadi M, Peitzman AB, Ferson PF, Luketich JD, and Landreneau RJ
- Subjects
- Aged, Aged, 80 and over, Cohort Studies, Debridement, Decompression, Surgical methods, Female, Follow-Up Studies, Humans, Kaplan-Meier Estimate, Lumbar Vertebrae pathology, Lumbar Vertebrae surgery, Magnetic Resonance Imaging methods, Male, Middle Aged, Neoplasm Invasiveness pathology, Neoplasm Staging, Osteomyelitis diagnosis, Patient Positioning methods, Perioperative Care methods, Postoperative Complications physiopathology, Postoperative Complications therapy, Proportional Hazards Models, Retrospective Studies, Risk Assessment, Severity of Illness Index, Spinal Fusion methods, Spinal Neoplasms pathology, Survival Analysis, Thoracic Vertebrae pathology, Thoracic Vertebrae surgery, Treatment Outcome, Osteomyelitis mortality, Osteomyelitis surgery, Spinal Neoplasms mortality, Spinal Neoplasms surgery, Thoracotomy methods
- Abstract
Background: Thoracic surgeons are commonly consulted to provide anterior thoracic exposure for infection and malignant neoplasms involving the thoracolumbar spine. These cases can present significant technical and management challenges secondary to the underlying pathology, associated anatomic inflammation, and impaired functional status. In this study, we review the perioperative outcomes in patients undergoing anterior spinal exposure for infection and neoplasm., Methods: 130 consecutive patients (61 women, 69 men) undergoing corpectomy, debridement, or debulking for osteomyelitis (n=50) or neoplasms (n=80) with decompression/stabilization at a single institution were analyzed. Primary endpoints included morbidity, mortality, and perioperative neurologic outcomes., Results: The mean age was 61.1 years. A cervical/sternotomy (n=8) approach was used for levels C7 to T2, thoracotomy (n=79) for levels T3 to T10, and thoracoabdominal (n=43) for T11 to L2 involvement. Primary spinal neoplasms (n=22, 16.9 %) and metastases (n=58, 44.6%) were treated with corpectomy and prosthetic stabilization and were associated with increased operative time (310 vs 243 minutes, p=0.02) and blood loss (825 vs 500 mL, p=0.002). Osteomyelitis was associated with longer hospital stays (12 vs 7 days, p<0.001). The 30-day and 90-day mortality was 9.2% and 20.8%, respectively. The major complication rate was 27.7%. The median length of stay was 9 days. Surgical intervention resulted in significant improvement in pain, numbness, weakness, and bowel and bladder dysfunction., Conclusions: Anterior spinal exposure represents an important modality in facilitating the treatment of patients with osteomyelitis, pathologic fractures, and spinal cord compression syndromes. These procedures are associated with a significant risk of morbidity and mortality, but they are effective in achieving spinal stabilization and alleviating neurologic symptoms., (Copyright © 2014 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2014
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25. Oesophageal carcinoma.
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Pennathur A, Gibson MK, Jobe BA, and Luketich JD
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- Adenocarcinoma etiology, Adenocarcinoma pathology, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Carcinoma, Squamous Cell etiology, Carcinoma, Squamous Cell pathology, Chemoradiotherapy, Endosonography, Esophagectomy, Humans, Lymph Node Excision, Neoadjuvant Therapy, Neoplasm Staging, Positron-Emission Tomography, Risk Factors, Esophageal Neoplasms diagnosis, Esophageal Neoplasms etiology, Esophageal Neoplasms pathology, Esophageal Neoplasms therapy
- Abstract
Oesophageal carcinoma affects more than 450,000 people worldwide and the incidence is rapidly increasing. Squamous-cell carcinoma is the predominant form of oesophageal carcinoma worldwide, but a shift in epidemiology has been seen in Australia, the UK, the USA, and some western European countries (eg, Finland, France, and the Netherlands), where the incidence of adenocarcinoma now exceeds that of squamous-cell types. The overall 5-year survival of patients with oesophageal carcinoma ranges from 15% to 25%. Diagnoses made at earlier stages are associated with better outcomes than those made at later stages. In this Seminar we discuss the epidemiology, pathophysiology, diagnosis and staging, management, prevention, and advances in the treatment of oesophageal carcinoma., (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Published
- 2013
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26. Thymic carcinoma: a multivariate analysis of factors predictive of survival in 290 patients.
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Weksler B, Dhupar R, Parikh V, Nason KS, Pennathur A, and Ferson PF
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- Female, Follow-Up Studies, Humans, Male, Middle Aged, Multivariate Analysis, Pennsylvania epidemiology, Prognosis, Retrospective Studies, Thymectomy, Thymoma surgery, Thymus Neoplasms surgery, Neoplasm Recurrence, Local mortality, SEER Program, Thymoma mortality, Thymus Neoplasms mortality
- Abstract
Background: Thymic carcinoma is a rare, aggressive disease with low 5-year survivals. We undertook this study to identify factors that impact prognosis and to better define the relationship between survival and surgical intervention., Methods: We queried the Surveillance, Epidemiology, and End Results cancer database and identified patients with thymic carcinoma. We performed univariate and multivariate analyses to identify factors prognostic for survival, focusing on demographic, tumor, and treatment variables., Results: For 290 patients with thymic carcinoma, the median survival was 48 months with 5-year survival of 30%. In multivariate analysis, type of surgical therapy (none, incomplete excision, complete thymic excision, debulking), Masaoka stage, and sex were important determinants of survival. Patients who underwent complete thymic excision had a significantly longer median survival than those who did not receive surgical therapy (105 versus 29 months; p < 0.001). In patients who underwent complete thymic excision, Masaoka stage and race were important determinants of survival in multivariate analysis., Conclusions: Complete thymic excision is the preferred primary treatment for thymic carcinoma. Masaoka stage has significant prognostic implications for all patients, including those who undergo complete thymic excision., (Copyright © 2013 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2013
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27. American College of Chest Physicians and Society of Thoracic Surgeons consensus statement for evaluation and management for high-risk patients with stage I non-small cell lung cancer.
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Donington J, Ferguson M, Mazzone P, Handy J Jr, Schuchert M, Fernando H, Loo B Jr, Lanuti M, de Hoyos A, Detterbeck F, Pennathur A, Howington J, Landreneau R, and Silvestri G
- Subjects
- Catheter Ablation, Humans, Neoplasm Staging, Pneumonectomy, Radiosurgery, Risk Assessment, Societies, Medical, United States, Carcinoma, Non-Small-Cell Lung pathology, Carcinoma, Non-Small-Cell Lung therapy, Disease Management
- Abstract
Background: The standard treatment of stage I non-small cell lung cancer (NSCLC) is lobectomy with systematic mediastinal lymph node evaluation. Unfortunately, up to 25% of patients with stage I NSCLC are not candidates for lobectomy because of severe medical comorbidity., Methods: A panel of experts was convened through the Thoracic Oncology Network of the American College of Chest Physicians and the Workforce on Evidence-Based Surgery of the Society of Thoracic Surgeons. Following a literature review, the panel developed 13 suggestions for evaluation and treatment through iterative discussion and debate until unanimous agreement was achieved., Results: Pretreatment evaluation should focus primarily on measures of cardiopulmonary physiology, as respiratory failure represents the greatest interventional risk. Alternative treatment options to lobectomy for high-risk patients include sublobar resection with or without brachytherapy, stereotactic body radiation therapy, and radiofrequency ablation. Each is associated with decreased procedural morbidity and mortality but increased risk for involved lobe and regional recurrence compared with lobectomy, but direct comparisons between modalities are lacking., Conclusions: Therapeutic options for the treatment of high-risk patients are evolving quickly. Improved radiographic staging and the diagnosis of smaller and more indolent tumors push the risk-benefit decision toward parenchymal-sparing or nonoperative therapies in high-risk patients. Unbiased assessment of treatment options requires uniform reporting of treatment populations and outcomes in clinical series, which has been lacking to date.
- Published
- 2012
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28. Surgical resection should be considered for stage I and II small cell carcinoma of the lung.
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Weksler B, Nason KS, Shende M, Landreneau RJ, and Pennathur A
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- Aged, Biopsy, Needle, Confidence Intervals, Databases, Factual, Disease-Free Survival, Education, Medical, Continuing, Female, Humans, Immunohistochemistry, Kaplan-Meier Estimate, Lung Neoplasms mortality, Lung Neoplasms radiotherapy, Male, Middle Aged, Neoplasm Staging, Pneumonectomy mortality, Pneumonectomy statistics & numerical data, Prognosis, Proportional Hazards Models, Radiotherapy, Adjuvant, Retrospective Studies, Risk Assessment, SEER Program, Small Cell Lung Carcinoma mortality, Small Cell Lung Carcinoma radiotherapy, Statistics, Nonparametric, Survival Analysis, Treatment Outcome, Lung Neoplasms pathology, Lung Neoplasms surgery, Pneumonectomy methods, Small Cell Lung Carcinoma pathology, Small Cell Lung Carcinoma surgery
- Abstract
Background: Small cell lung carcinoma (SCLC) is rarely treated with resection, either alone or combined with other modalities. This study evaluated the role of surgical resection in the treatment of stage I and II SCLC., Methods: We queried the Surveillance, Epidemiology, and End Results (SEER) database for patients from 1988 to 2007 with SCLC. Survival was determined by Kaplan-Meier analysis and compared using the log-rank test. A Cox proportional hazard model identified relevant survival variables., Results: We identified 3,566 patients with stage I or II SCLC. Lung resection was performed in 895 (25.1%), wedge resection in 251 (28.0%), lobectomy or pneumonectomy in 637 (71.2%), and lung resection not otherwise specified in 7 (0.78%). Median survival was 34.0 months (95% confidence interval [CI], 29.0 to 39.0 months) vs 16.0 months (95% CI, 15.3 to 16.7; p<0.001) in nonsurgical patients. Median survival after lobectomy or pneumonectomy was 39.0 months (95% CI, 30.7 to 40.3) and significantly longer than after wedge resection (28.0 months; 95% CI, 23.2 to 32.8; p=0.001). However, survival after wedge resection was still significantly longer than survival in nonsurgical patients (p<0.001). Sex (p=0.013), age, stage at diagnosis, radiotherapy, and operation (all p<0.001) significantly affected survival. In the surgical patients, sex (p=0.001), age (p<0.001), final stage (p<0.001), and type of resection (p=0.01) were important determinants of survival., Conclusions: Surgical resection as a component of treatment for stage I or II SCLC is associated with significantly improved survival and should be considered in the management of early-stage SCLC., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2012
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29. The role of adjuvant radiation therapy for resected stage III thymoma: a population-based study.
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Weksler B, Shende M, Nason KS, Gallagher A, Ferson PF, and Pennathur A
- Subjects
- Adult, Age Factors, Aged, Cohort Studies, Combined Modality Therapy, Disease-Free Survival, Female, Humans, Kaplan-Meier Estimate, Male, Middle Aged, Multivariate Analysis, Neoplasm Staging, Prospective Studies, Radiotherapy, Adjuvant, SEER Program, Thymoma mortality, Thymoma pathology, Thymus Neoplasms mortality, Thymus Neoplasms pathology, Thymectomy, Thymoma radiotherapy, Thymoma surgery, Thymus Neoplasms radiotherapy, Thymus Neoplasms surgery
- Abstract
Background: Because of the rarity of the disease and long survival of most patients, the role of adjuvant radiation therapy in patients with surgically resected stage III thymoma is unclear, and few prospective studies are available. The objective was to evaluate the impact of postoperative radiation therapy after resection of stage III thymoma., Methods: The Surveillance, Epidemiology, and End Results (SEER) database was queried for all patients with stage III thymoma who underwent surgical therapy and survived more than 30 days after diagnosis. Survival was estimated with the Kaplan-Meier method. The hazard ratio for death was determined using a Cox proportional hazard model., Results: There were 476 patients with stage III thymoma identified who underwent surgical therapy, did not receive preoperative radiotherapy, and had complete SEER records with regard to radiation treatment. Postoperative radiation therapy was given to 322 patients (67.6%). Patients who received postoperative radiation therapy were younger and had a higher rate of debulking surgery than patients who did not. Patients receiving postoperative radiation had a median overall survival of 127 months (95% confidence interval, 100.9 to 153.1) compared with 105 months (95% confidence interval, 76.9 to 133.1) in patients treated with surgery alone (p=0.038). However, in multivariate analysis, postoperative radiation was not a significant factor affecting overall survival. Disease-specific survival was significantly improved in the adjuvant radiation group, and in multivariate analysis, improved outcomes were associated with postoperative radiation (p=0.049)., Conclusions: In this large population-based study, most patients with stage III thymoma were treated with adjuvant radiation. Postoperative radiation was associated with improved disease-specific survival, but not improved overall survival., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
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- 2012
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30. Anatomic segmentectomy for the solitary pulmonary nodule and early-stage lung cancer.
- Author
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Schuchert MJ, Abbas G, Awais O, Pennathur A, Nason KS, Wilson DO, Siegfried JM, Luketich JD, and Landreneau RJ
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Disease-Free Survival, Female, Humans, Lung Neoplasms mortality, Lung Neoplasms pathology, Lung Neoplasms secondary, Male, Middle Aged, Neoplasm Recurrence, Local mortality, Neoplasm Recurrence, Local pathology, Neoplasm Staging, Postoperative Complications mortality, Precancerous Conditions mortality, Precancerous Conditions pathology, Retrospective Studies, Solitary Pulmonary Nodule mortality, Solitary Pulmonary Nodule pathology, Survival Rate, Young Adult, Lung Neoplasms surgery, Pneumonectomy methods, Precancerous Conditions surgery, Solitary Pulmonary Nodule surgery, Thoracic Surgery, Video-Assisted methods
- Abstract
Background: Anatomic segmentectomy is a versatile sublobar resection approach that can be both diagnostic and therapeutic in the setting of the indeterminate pulmonary nodule (IPN), metastasectomy, as well as small, peripheral cancers. We analyzed the clinical indications and perioperative outcomes after anatomic segmentectomy and explored its utility in the diagnosis and treatment of IPNs and small stage IA lung cancers., Methods: This study is a retrospective review of 785 consecutive patients undergoing anatomic segmentectomy from 2002 to 2010. Primary outcome variables include perioperative course, morbidity, mortality, recurrence patterns, and survival., Results: Surgical indications included IPN (62.4%), known lung cancer (27.6%), suspected metastasis (4.1%), bullous disease (3.7%), or other (2.2%). Video-assisted thoracic surgery was employed in 468 (59.6%) and open thoracotomy in 317 (40.4%) patients. Median length of stay was 6 days. Overall complication rate was 34.9%. Thirty-day mortality was 1.1%. Among 490 patients with an IPN, 381 (77.7%) were found to have lung cancer, 41 (8.4%) metastatic cancer, and 68 (13.9%) benign disease. Among patients with pathologic stage IA lung cancer, there was no difference in recurrence rates (14.5% vs 13.9%) or 5-year freedom from recurrence estimates (78% in each group, p=0.738) when comparing segmentectomy and lobectomy., Conclusions: Anatomic segmentectomy provides acceptable morbidity and mortality when approaching the IPN. Cancer is identified in 86% of lesions. Complete surgical resection can be achieved with generous parenchymal margins and thorough nodal staging for small, peripheral stage IA non-small cell lung cancer. The use of anatomic segmentectomy should be considered in this era of competing image-guided diagnostic and therapeutic approaches to peripheral lung pathology., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2012
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31. Extended Chamberlain minithoracotomy: a safe and versatile approach for difficult lung resections.
- Author
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Schuchert MJ, Souza AP, Abbas G, Pennathur A, Nason KS, Jack R, Horne ZD, Landreneau JR, Santana M, Wilson DO, Luketich JD, and Landreneau RJ
- Subjects
- Adult, Aged, Aged, 80 and over, Cohort Studies, Female, Humans, Length of Stay, Lung Neoplasms mortality, Lung Neoplasms pathology, Lung Neoplasms therapy, Male, Middle Aged, Neoadjuvant Therapy methods, Pain, Postoperative physiopathology, Patient Positioning, Patient Selection, Retrospective Studies, Risk Assessment, Safety Management, Supine Position, Treatment Outcome, Young Adult, Lung Neoplasms surgery, Minimally Invasive Surgical Procedures methods, Pneumonectomy methods, Thoracotomy methods
- Abstract
Background: We present the perioperative outcomes of patients undergoing an anterior "extended Chamberlain" minithoracotomy as an alternative approach to a hemi-clamshell sternotomy or extended lateral thoracotomy for safe and reliable access to the pulmonary hilum and subsequent anatomic pulmonary resection., Methods: This study is a retrospective review of 162 patients undergoing anatomic lung resection through a mini anterior thoracotomy from 2002 to 2010. An 8-cm anterior thoracotomy was performed with the patient in a supine position, entering the chest through the second intercostal space. The pectoralis muscle fibers were split with preservation of the mammary artery medially and the thoracoacromial neurovascular bundle laterally. Primary outcome variables included hospital course, complications, and mortality rate., Results: The mean age was 63.9 (range, 20 to 85 years); female to male ratio was 71:91. Neoadjuvant therapy was used in 49 (30.2%) patients. Proposed resections were successful in 161 of 162 (99%) patients. Conversion to hemi-clamshell was required in 1 patient for vascular control. Complications occurred in 48 (29.6%) patients. Three (1.9%) perioperative deaths (2 pneumonectomies [6.3%], 1 lobectomy [1.0%]) occurred. Median length of stay was 8 days., Conclusions: The "extended Chamberlain" mini anterior thoracotomy provides direct and expeditious, less-invasive access to the pulmonary hilum. This approach preserves muscle function and avoids partial sternotomy or extended lateral thoracotomy, and their associated incisional-related morbidity., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2012
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32. Comparative genomics of esophageal adenocarcinoma and squamous cell carcinoma.
- Author
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Bandla S, Pennathur A, Luketich JD, Beer DG, Lin L, Bass AJ, Godfrey TE, and Litle VR
- Subjects
- Cohort Studies, Genome, Genomics, Humans, Oligonucleotide Array Sequence Analysis, Oncogenes, Polymorphism, Single Nucleotide, Adenocarcinoma genetics, Carcinoma, Squamous Cell genetics, DNA Copy Number Variations, Esophageal Neoplasms genetics
- Abstract
Background: Esophageal cancer consists of two major histologic types: esophageal squamous cell carcinoma (ESCC), predominant globally, and esophageal adenocarcinoma (EAC), which has a higher incidence in westernized countries. Five-year overall survival is 15%. Clinical trials frequently combine histologic types although they are different diseases with distinct origins. In the evolving era of personalized medicine and targeted therapies, we hypothesized that ESCC and EAC have genomic differences important for developing new therapeutic strategies for esophageal cancer., Methods: We explored DNA copy number abnormalities in 70 ESCCs with publicly available array data and 189 EACs from our group. All data was from single nucleotide polymorphism arrays. Analysis was performed using a segmentation algorithm. Log ratio thresholds for copy number gain and loss were set at ±0.2 (approximately 2.3 and 1.7 copies, respectively)., Results: The ESCC and EAC genomes showed some copy number abnormalities with similar frequencies (eg, CDKN2A, EGFR, KRAS, MYC, CDK6, MET) but also many copy number abnormalities with different frequencies between histologic types, most of which were amplification events. Some of these regions harbor genes for which targeted therapies are currently available (VEGFA, ERBB2) or for which agents are in clinical trials (PIK3CA, FGFR1). Other regions contain putative oncogenes that may be targeted in the future., Conclusions: Using single nucleotide polymorphism arrays we compared genomic abnormalities in a large cohort of EACs and ESCCs. We report here the similar and different frequencies of copy number abnormalities in ESCC and EAC. These results may allow development of histology-specific therapeutic agents for esophageal cancer., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2012
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33. Influence of age and IB status after resection of node-negative non-small cell lung cancer.
- Author
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Schuchert MJ, Awais O, Abbas G, Horne ZD, Nason KS, Pennathur A, Souza AP, Siegfried JM, Wilson DO, Luketich JD, and Landreneau RJ
- Subjects
- Adult, Age Factors, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Neoplasm Invasiveness, Retrospective Studies, Young Adult, Carcinoma, Non-Small-Cell Lung pathology, Carcinoma, Non-Small-Cell Lung surgery, Lung Neoplasms pathology, Lung Neoplasms surgery, Pneumonectomy methods
- Abstract
Background: Anatomic segmentectomy has been proposed as a reasonable alternative to lobectomy in the management of small early-stage non-small cell lung cancers. We reviewed our outcomes with anatomic segmentectomy versus lobectomy for stages IA and IB non-small cell lung cancer stratified by age and stage., Methods: We conducted a retrospective review of prospectively-collected data analyzing outcomes after anatomic segmentectomy (n=305) for stage IA (n=187) or IB (n=118) NSCLC from 1999 to 2010. Lobectomy was performed in 594 patients for stage IA (n=290) and IB (n=304) disease during the same period. Surgical approach was stratified by stage and by the following age groups: less than 70, 70 to 79, and 80 or greater. Primary outcome variables included complications, mortality, recurrence patterns, and survival. Mean follow-up was 37 months., Results: Segmentectomy was associated with reduced complications (43.6% vs 58.7%) and mortality (0% vs 7.8%) in patients greater than 80 years old, without a difference in recurrence rates. There was no difference in complications or mortality in the younger age groups. Freedom from recurrence was similar between segmentectomy and lobectomy for stage IA tumors across all age groups. A reduced recurrence-free survival was seen with segmentectomy for stage IB tumors, especially with visceral pleural invasion (median 22.7 vs 29.6 months), p=0.048)., Conclusions: Segmentectomy appears to be a reasonable approach for early-stage NSCLC in patients 80 years of age or greater due to reduced morbidity and mortality with equivalent freedom from recurrence. Although equivalent survival was seen in all age groups for stage IA, these data further support the use of lobectomy for resection of stage IB tumors., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
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- 2012
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34. Postesophagectomy chylothorax: incidence, risk factors, and outcomes.
- Author
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Shah RD, Luketich JD, Schuchert MJ, Christie NA, Pennathur A, Landreneau RJ, and Nason KS
- Subjects
- Aged, Chylothorax surgery, Female, Humans, Incidence, Male, Middle Aged, Postoperative Complications epidemiology, Retrospective Studies, Risk Factors, Treatment Outcome, Chylothorax epidemiology, Chylothorax etiology, Esophagectomy adverse effects
- Abstract
Background: Chylothorax is a rare but potentially lethal complication of esophagectomy. This study evaluated the rate of postesophagectomy chylothorax, identified associated risk factors, and compared postoperative outcomes in patients with and without chylothorax., Methods: We reviewed 892 consecutive patients who underwent esophagectomy (1997 to 2008). Preoperative, operative, and postoperative details, including adverse outcomes and mortality, were analyzed., Results: Postesophagectomy chylothorax occurred in 34 patients (3.8%). Chylothorax was significantly associated with 30-day major complications (85% vs 46%; p<0.001), including an increased likelihood of sepsis (p=0.001), pneumonia (p=0.009), reintubation (p=0.002) or reoperation (p<0.001), and death (17.7% vs 3.9%, p<0.001). Median length of stay was 17 vs 8 days (p=0.005). Median time to chylothorax diagnosis was 5 days. Thoracic duct ligation was performed in 21 (62%) at a median 13 days after esophagectomy. Two patients required repeat duct ligation for persistent chylothorax. Squamous cell cancer histology (9 of 34; 26%) was an independent predictor of postoperative chylothorax (odds ratio, 4.18; 95% confidence interval, 1.39 to 12.6). Odds of chylothorax were 36 times greater with average daily chest tube output exceeding 400 mL in the first 6 postoperative days (odds ratio, 35.9; 95% confidence interval, 8.2 to 157.8)., Conclusions: Postoperative chylothorax is associated with significant postoperative morbidity and mortality. Patients with squamous cell cancer may be at increased risk. In addition, average daily chest tube output exceeding 400 mL in the early postoperative period should prompt fluid analysis for chylothorax to facilitate early diagnosis and consideration of thoracic duct ligation., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2012
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35. Thymomas and extrathymic cancers.
- Author
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Weksler B, Nason KS, Mackey D, Gallagher A, and Pennathur A
- Subjects
- Adult, Aged, Aged, 80 and over, Causality, Female, Humans, Incidence, Male, Middle Aged, Retrospective Studies, Neoplasms, Multiple Primary epidemiology, Thymoma epidemiology, Thymus Neoplasms epidemiology
- Abstract
Background: Patients with thymoma may have a predisposition toward extrathymic neoplasia. To understand the lifetime risk and incidence of extrathymic neoplasia in patients with thymoma, we evaluated extrathymic neoplasms diagnosed either before or after the diagnosis of thymoma., Methods: We queried the Surveillance, Epidemiology, and End Results (SEER) cancer database and identified patients with thymoma and extrathymic neoplasms. We collected demographic and treatment data, calculated the incidence of each extrathymic neoplasm (adjusting for age), and compared the incidence of extrathymic neoplasm in patients with thymoma with the age-adjusted incidence in the SEER database general population., Results: Of 2,171 patients with thymoma in the SEER database, 306 (14.1%) had extrathymic primary cancers. Extrathymic neoplasms were diagnosed before the diagnosis of thymoma in 88 patients and after the diagnosis of thymoma in 206 patients. In 12 patients, separate extrathymic neoplasms were diagnosed both before and after thymoma diagnosis. The incidence of extrathymic cancers in patients with thymoma (8,224 per 100,000 persons) was significantly higher than in the SEER general population (459 per 100,000 persons; p<0.001). The standardized incidence ratio for extrathymic cancer was also significantly increased, in particular for lymphomas, leukemias, esophageal cancer, and lung cancer. Increased age at diagnosis (p<0.001), longer survival after diagnosis (p<0.001), and male sex (p=0.041)-but not radiation therapy or surgery-were significant risk factors for the development of extrathymic cancers in patients with thymoma., Conclusions: The incidence of extrathymic neoplasia is significantly higher in patients with thymoma than in the general population and occurs both before and after the diagnosis of thymoma., (Copyright © 2012 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2012
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36. Quality of life after collis gastroplasty for short esophagus in patients with paraesophageal hernia.
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Nason KS, Luketich JD, Awais O, Abbas G, Pennathur A, Landreneau RJ, and Schuchert MJ
- Subjects
- Aged, Female, Humans, Male, Retrospective Studies, Fundoplication, Gastroplasty, Hernia, Hiatal surgery, Laparoscopy, Quality of Life
- Abstract
Background: Collis gastroplasty is an important component of laparoscopic giant paraesophageal hernia (GPEH) repair in patients with persistent shortened esophagus after aggressive laparoscopic mobilization. Concerns remain, however, regarding symptomatic outcomes compared with fundoplication alone. This study assessed the impact of Collis gastroplasty on quality of life after laparoscopic GPEH repair., Methods: We performed 795 nonemergent laparoscopic GPEH repairs with fundoplication (with Collis, n = 454; fundoplication alone, n = 341). Radiographic follow-up and symptom assessment were obtained a median 22 months and 20 months, respectively, after fundoplication alone and 36 and 33 months, respectively, after Collis (p < 0.001). Radiographic recurrence, reoperation for recurrent hernia or intolerable symptoms, overall symptom improvement, and quality of life were examined., Results: Compared with fundoplication alone, Collis patients had significantly larger GPEH (p = 0.027) and fewer comorbidities (p = 0.002). Radiographic recurrences were similar (p = 0.353). Symptom improvement was significant for both (p < 0.001), although Collis was associated with better pain resolution (p < 0.001) and less gas bloat (p = 0.003). Quality of life was good to excellent in 88% (90% Collis versus 86% fundoplication alone, p = 0.17)., Conclusions: Symptomatic outcomes after laparoscopic fundoplication with Collis gastroplasty are excellent and comparable with those of fundoplication alone. These results confirm that utilization of Collis gastroplasty, based on intraoperative assessment for shortened esophagus, is not detrimental to the overall outcome or quality of life associated with the laparoscopic approach to GPEH. Collis gastroplasty is recommended as an important procedure in the surgeon's armamentarium for laparoscopic repair of GPEH., (Copyright © 2011 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2011
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37. Reoperative antireflux surgery for failed fundoplication: an analysis of outcomes in 275 patients.
- Author
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Awais O, Luketich JD, Schuchert MJ, Morse CR, Wilson J, Gooding WE, Landreneau RJ, and Pennathur A
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Anastomosis, Surgical methods, Endoscopy, Gastrointestinal, Esophagus physiopathology, Female, Follow-Up Studies, Gastroesophageal Reflux epidemiology, Gastroesophageal Reflux etiology, Humans, Incidence, Male, Manometry, Middle Aged, Obesity surgery, Pennsylvania epidemiology, Pressure, Quality of Life, Retrospective Studies, Surveys and Questionnaires, Treatment Failure, Young Adult, Esophagus surgery, Fundoplication adverse effects, Gastroesophageal Reflux surgery, Gastroplasty methods, Reoperation methods, Stomach surgery
- Abstract
Background: With an increase in the performance of laparoscopic antireflux procedures, more patients with a failed primary antireflux operation are being referred to thoracic surgeons for complex redo procedures. The objective of this study was to evaluate our results of redo antireflux surgery., Methods: We conducted a retrospective review of patients who underwent redo surgery for failed fundoplication. The primary endpoint was failure of the redo operation; other endpoints included gastroesophageal reflux disease-health-related quality of life (HRQOL) after redo fundoplication., Results: A total of 275 patients (median age, 52 years; range, 17 to 88 years; men 82, women 193) underwent redo antireflux surgery. The most common pattern of failure of the initial operation was transmediastinal migration-recurrent hernia in 177 patients (64%). Redo surgery included Nissen fundoplication in 200 (73%), Collis gastroplasty in 119 (43%), and partial fundoplication in 41 (15%). There was no perioperative mortality. At a median follow-up of 39.6 months, 31 patients (11.2%) had a failure of the redo surgery, requiring reoperation. The two-year estimated probability of freedom from failure was 93% (95% confidence interval 89% to 96%). The HRQOL scores, available for 186 patients, were excellent to satisfactory in 85.5%, and poor in 14.5%., Conclusions: Redo antireflux surgery can be performed safely in experienced centers with outcomes that are similar to published open results. Complete takedown and reestablishment of the normal anatomy, recognition of a short esophagus, and proper placement of the wrap are essential components of the procedure. Thoracic surgeons with significant laparoscopic and open esophageal surgical experience can perform minimally invasive, complex redo esophageal antireflux procedures safely with good results., (Copyright © 2011 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2011
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38. Oncologic outcomes after surgical resection of subcentimeter non-small cell lung cancer.
- Author
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Schuchert MJ, Kilic A, Pennathur A, Nason KS, Wilson DO, Luketich JD, and Landreneau RJ
- Subjects
- Aged, Aged, 80 and over, Carcinoma, Non-Small-Cell Lung mortality, Carcinoma, Non-Small-Cell Lung pathology, Female, Humans, Lung Neoplasms mortality, Lung Neoplasms pathology, Male, Middle Aged, Neoplasm Recurrence, Local, Postoperative Complications etiology, Thoracic Surgery, Video-Assisted, Treatment Outcome, Carcinoma, Non-Small-Cell Lung surgery, Lung Neoplasms surgery
- Abstract
Background: The recent initiation of screening protocols and greater utilization of computed tomography has led to an increasing proportion of non-small cell lung cancer (NSCLC) patients presenting with subcentimeter stage IA tumors. The aim of this study was to compare the oncologic outcomes of lobectomy, segmentectomy, and wedge resection in patients with NSCLC tumors 1 cm or less in diameter., Methods: Data were extracted from medical records of patients undergoing surgical resection for stage IA NSCLC and a pathologically confirmed tumor diameter measuring 1 cm or less. Primary oncologic outcomes were disease recurrence and disease-free survival. Statistical comparisons were performed using Fisher's exact test and unpaired t test. Kaplan-Meier curves were compared using the log rank test. Significance was defined as a two-tailed p value less than 0.05., Results: A total of 107 patients underwent complete (R0) surgical resection for stage IA NSCLC 1 cm or less in diameter (lobectomy, 32; segmentectomy, 40; wedge, 35). Age, sex distribution, tumor size, and histology were similar between groups. There was 1 perioperative mortality in the lobectomy group (3%). At a mean follow-up of 42.5 months, overall disease recurrence was equivalent, occurring in 3 lobectomy patients (9%), 4 segmentectomy patients (10%), and 3 wedge resection patients (9%; p=0.99). Estimated 5-year disease-free survival was comparable among cohorts (lobectomy, 87%; segmentectomy, 89%; wedge, 89%; p>0.402)., Conclusions: Sublobar resections are associated with oncologic outcomes that are comparable to those of lobectomy for subcentimeter stage IA NSCLC, suggesting that they may be appropriate surgical interventions in this patient cohort. The validity of these observations needs to be assessed in a prospective setting., (Copyright © 2011 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2011
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39. MicroRNA prognostic signature for nodal metastases and survival in esophageal adenocarcinoma.
- Author
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Feber A, Xi L, Pennathur A, Gooding WE, Bandla S, Wu M, Luketich JD, Godfrey TE, and Litle VR
- Subjects
- Adenocarcinoma genetics, Adenocarcinoma secondary, Adenocarcinoma surgery, Aged, Biomarkers, Tumor analysis, Cohort Studies, Disease-Free Survival, Esophageal Neoplasms genetics, Esophageal Neoplasms surgery, Esophagectomy methods, Esophagectomy mortality, Female, Humans, Lymphatic Metastasis, Male, MicroRNAs genetics, Middle Aged, Multivariate Analysis, Neoplasm Invasiveness pathology, Neoplasm Staging, Predictive Value of Tests, Prognosis, Proportional Hazards Models, Retrospective Studies, Reverse Transcriptase Polymerase Chain Reaction, Survival Analysis, Adenocarcinoma mortality, Biomarkers, Tumor genetics, Esophageal Neoplasms mortality, Gene Expression Regulation, Neoplastic, MicroRNAs analysis
- Abstract
Background: The incidence of esophageal adenocarcinoma is rapidly increasing and is now one of the leading causes of cancer death in the western world. MicroRNAs (miRNAs) are small noncoding RNAs that regulate the expression of protein-encoding genes and are involved in the development, progression and prognosis of other malignancies. We hypothesized that global miRNA expression would predict survival and lymph node involvement in a cohort of surgically resected esophagus cancer patients., Methods: The miRNA analysis was performed using a custom Affymetrix microarray with probes for 462 known human, 2,102 predicted human, 357 mouse, and 238 rat miRNAs. Expression of miRNA was evaluated in 45 primary tumors, and the association of miRNA expression with patient survival and lymph node metastasis was assessed. The prognostic impact of identified unique miRNAs was verified with quantitative reverse transcriptase polymerase chain reaction., Results: Our data indicate that the expression of individual human miRNA species is significantly associated with postresection patient survival. Using data from five unique miRNAs, we were further able to generate a combined miRNA expression signature that is associated with patient survival (p=0.005; hazard ratio 3.6) independent of node involvement and overall stage. The expression of three miRNAs (miR-99b and miR-199a_3p and _5p) was also associated with the presence of lymph node metastasis., Conclusions: These results suggest miRNA expression profiling could provide prognostic utility in staging esophagus cancer patients and treatment planning with endoscopic and neoadjuvant therapies. The alterations of specific miRNAs may further elucidate steps in the metastatic pathway and allow for development of targeted therapy., (Copyright © 2011 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2011
- Full Text
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40. Impact of angiolymphatic and pleural invasion on surgical outcomes for stage I non-small cell lung cancer.
- Author
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Schuchert MJ, Schumacher L, Kilic A, Close J, Landreneau JR, Pennathur A, Awais O, Yousem SA, Wilson DO, Luketich JD, and Landreneau RJ
- Subjects
- Adult, Aged, Aged, 80 and over, Carcinoma, Non-Small-Cell Lung surgery, Female, Humans, Lung Neoplasms surgery, Lymphatic Metastasis, Male, Middle Aged, Neoplasm Invasiveness, Neoplasm Staging, Retrospective Studies, Treatment Outcome, Young Adult, Carcinoma, Non-Small-Cell Lung pathology, Lung Neoplasms pathology, Pleural Neoplasms pathology
- Abstract
Background: In the current study, we analyze the impact of pathologic variables (angiolymphatic invasion, visceral pleural invasion, and tumor inflammation) upon survival outcomes after segmentectomy or lobectomy for stage I non-small cell lung cancer., Methods: A retrospective review was made of 524 patients undergoing resection of stage I non-small cell lung cancer through either lobectomy (n = 285) or anatomic segmentectomy (n = 239). Primary outcome variables include recurrence-free and overall survival. Statistical comparisons were performed with the t test and Fisher's exact test. Recurrence-free and overall survival was estimated utilizing the Kaplan-Maier method, with statistical significance being assessed by the log rank test., Results: The incidence of angiolymphatic invasion, visceral pleural invasion, and degree of tumor inflammation, as well as morbidity, mortality, and length of stay were similar between segmentectomy and lobectomy. The presence of angiolymphatic invasion or visceral pleural invasion was associated with a significant decrease in recurrence-free survival (p < 0.01) and overall survival (p < 0.01). There was a trend for decreased recurrence with increasing tumor inflammation (mild versus severe, p = 0.066). There was no difference in rates of local recurrence (5.6% versus 7.9%, p = 0.59) or survival (p = 0.455) between segmentectomy and lobectomy, respectively., Conclusions: Angiolymphatic and visceral pleural invasion appear to be strong adverse prognostic factors after anatomic resection by segmentectomy or lobectomy for stage I non-small cell lung cancer. Overall survival is not affected by the extent of anatomical surgical resection. These data may have implications regarding the role of adjuvant systemic therapy after surgical resection for tumors with these pathologic characteristics., (Copyright © 2011 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2011
- Full Text
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41. Minimally invasive redo antireflux surgery: lessons learned.
- Author
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Pennathur A, Awais O, and Luketich JD
- Subjects
- Gastroesophageal Reflux diagnosis, Humans, Minimally Invasive Surgical Procedures methods, Reoperation, Treatment Failure, Gastroesophageal Reflux surgery
- Abstract
Reoperative antireflux procedures are traditionally approached through an open technique. However, with increasing experience in minimally invasive antireflux procedures, more reoperative procedures are being performed laparoscopically. The success rate for reoperative surgery, either open or laparoscopic, does not equal that of primary antireflux operations. Redo antireflux surgery is a complex operation and a thorough evaluation prior to treatment is essential. There are several options for failed primary antireflux surgery including reconstructive options, such as redo fundoplication and Roux-en Y near esophagojejunostomy. In some cases of anatomic disruption, esophagectomy is required. In this article, we discuss the following: clinical presentation; the evaluation of patients; causes of failure; and choice of operation with a focus on reconstructive options, and technical aspects of minimally invasive redo antireflux surgery. We describe our experience and summarize the lessons learned., (2010 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2010
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42. The "best operation" for esophageal cancer?
- Author
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Pennathur A, Zhang J, Chen H, and Luketich JD
- Subjects
- Anastomosis, Surgical, Esophagus surgery, Humans, Lymph Node Excision, Minimally Invasive Surgical Procedures, Esophageal Neoplasms surgery, Esophagectomy methods
- Abstract
There are several controversies in the surgical management of esophageal cancer including the surgical approach, extent of resection, optimal fields of lymph node dissection, and the ideal location of anastomosis. Optimal surgical treatment strategies must include accurate staging and the selection of an appropriate surgical approach. In addition, other considerations include complete resection, lymph node dissection and evaluation of oncologic and functional outcomes. The objective of this article is to review the literature and discuss our surgical approach to esophageal cancer., (2010 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2010
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43. Technique of minimally invasive Ivor Lewis esophagectomy.
- Author
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Pennathur A, Awais O, and Luketich JD
- Subjects
- Humans, Laparoscopy, Minimally Invasive Surgical Procedures, Thoracoscopy, Esophageal Neoplasms surgery, Esophagectomy methods
- Abstract
Since the initial description of laparoscopic fundoplication, surgeons have increasingly incorporated the techniques of minimally invasive surgery in the surgical management of esophageal diseases. Minimally invasive surgical techniques have been more frequently applied for benign esophageal disease, and are now being used for malignant disease. There are several approaches, which include the transthoracic and transhiatal approaches, for esophageal resection for cancer. The objective of this article is to describe our technique of minimally invasive Ivor Lewis esophagectomy., (2010 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Published
- 2010
- Full Text
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44. Stereotactic radiosurgery for the treatment of lung neoplasm: experience in 100 consecutive patients.
- Author
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Pennathur A, Luketich JD, Heron DE, Schuchert MJ, Burton S, Abbas G, Gooding WE, Ferson PF, Ozhasoglu C, Gilbert S, Landreneau RJ, and Christie NA
- Subjects
- Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Retrospective Studies, Lung Neoplasms surgery, Radiosurgery
- Abstract
Background: Surgical resection is the standard of care for patients with resectable non-small cell lung cancer or selected patients with pulmonary metastases. Stereotactic radiosurgery may offer an alternative option for high-risk patients who are not surgical candidates. We report our initial experience with stereotactic radiosurgery in the treatment of lung neoplasm in 100 consecutive patients., Methods: Patients who were medically inoperable were offered stereotactic radiosurgery. Thoracic surgeons evaluated all patients, placed fiducials, and performed treatment planning in collaboration with radiation oncologists. Initially, a median dose of 20 Gy prescribed to the 80% isodose line was administered in a single fraction, and this was subsequently increased to a total of 60 Gy in three fractions. The primary end point evaluated was overall survival., Results: We treated 100 patients (median age, 70 years; 51 men, 49 women) with stereotactic radiosurgery: 46 (46%) with primary lung neoplasm, 35 (35%) with recurrent cancer, and 19 (19%) with pulmonary metastases. The median follow-up was 20 months. The median overall survival was 24 months. Local recurrence occurred in 25 patients. The probability of 2-year overall survival was 50% for the entire group, 44% for primary lung cancer, 41% for recurrent cancer, and 84% for metastatic cancer., Conclusions: Our initial experience indicates that stereotactic radiosurgery has reasonable results in these high-risk patients. Resection continues to remain the standard treatment; however, stereotactic radiosurgery may offer an alternative in high-risk patients. Further prospective studies with different dose schema are needed to evaluate the efficacy of stereotactic radiosurgery.
- Published
- 2009
- Full Text
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45. Image-guided radiofrequency ablation of lung neoplasm in 100 consecutive patients by a thoracic surgical service.
- Author
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Pennathur A, Abbas G, Gooding WE, Schuchert MJ, Gilbert S, Christie NA, Landreneau RJ, and Luketich JD
- Subjects
- Adult, Aged, Aged, 80 and over, Humans, Lung Neoplasms mortality, Middle Aged, Retrospective Studies, Survival Rate, Thoracic Surgery, Catheter Ablation methods, Lung Neoplasms diagnostic imaging, Lung Neoplasms surgery, Tomography, X-Ray Computed
- Abstract
Background: Surgical resection is the standard of care for patients with resectable non-small cell lung cancer or selected patients with pulmonary metastases. However, for high-risk patients radiofrequency ablation (RFA) may offer an alternative option. The objective of this study was to evaluate computed tomography-guided RFA for high-risk patients and report our initial experience in 100 consecutive patients by a thoracic surgical service., Methods: Medically inoperable patients were offered RFA. Thoracic surgeons evaluated and performed RFA under computed tomography guidance. Patients were followed in the thoracic surgery clinic. The primary end point evaluated was overall survival., Results: One hundred patients underwent image-guided RFA for lung neoplasm (40 men, 60 women; median age, 73.5 years; range, 26 to 95 years). Forty-six patients (46%) with primary lung neoplasm, 25 patients (25%) with recurrent cancer, and 29 patients (29%) with pulmonary metastases underwent RFA. The mean follow-up for alive patients was 17 months. The median overall survival for the entire group of patients was 23 months. The probabilities of 2-year overall survival for the entire group, primary lung cancer patients, recurrent cancer patients, and metastatic cancer patients were 49% (95% confidence interval, 37 to 60), 50% (95% confidence interval, 33 to 65), 55% (95% confidence interval, 25 to 77), and 41% (95% confidence interval, 19 to 62), respectively., Conclusions: Our experience indicates that image-guided RFA done by the thoracic surgeons is feasible and safe in high-risk patients with lung neoplasm with reasonable results in patients who are not fit for surgery. Thoracic surgeons can perform RFA safely, and should continue to investigate this new image-guided modality that may offer an alternative option in medically inoperable patients.
- Published
- 2009
- Full Text
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46. Endobronchial ultrasound as a diagnostic tool in patients with mediastinal lymphadenopathy.
- Author
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Gilbert S, Wilson DO, Christie NA, Pennathur A, Luketich JD, Landreneau RJ, Close JM, and Schuchert MJ
- Subjects
- Adult, Aged, Aged, 80 and over, Biopsy, Needle, Carcinoma, Non-Small-Cell Lung pathology, Carcinoma, Small Cell pathology, Female, Humans, Image Processing, Computer-Assisted, Lung Neoplasms pathology, Lung Neoplasms secondary, Lymph Nodes diagnostic imaging, Lymph Nodes pathology, Lymphatic Diseases pathology, Lymphatic Metastasis pathology, Male, Mediastinal Neoplasms pathology, Mediastinoscopy, Middle Aged, Positron-Emission Tomography, Sarcoidosis, Pulmonary diagnostic imaging, Sarcoidosis, Pulmonary pathology, Sensitivity and Specificity, Tomography, X-Ray Computed, Young Adult, Carcinoma, Non-Small-Cell Lung diagnostic imaging, Carcinoma, Small Cell diagnostic imaging, Endosonography methods, Lung Neoplasms diagnostic imaging, Lymphatic Diseases diagnostic imaging, Lymphatic Metastasis diagnostic imaging, Mediastinal Neoplasms diagnostic imaging, Ultrasonography, Interventional methods
- Abstract
Background: The diagnostic yield and accuracy of new approaches to diagnose cancer should focus on comparison with established surgical techniques. Our objective was to evaluate the diagnostic performance of endobronchial ultrasound (EBUS) to detect cancer in patients with radiographically abnormal mediastinal lymph nodes., Methods: The medical records of patients who underwent EBUS and had abnormal mediastinal lymph nodes (short-axis >1 cm and [or] positron emission topography-positive) over a 25 month period at the University of Pittsburgh were reviewed. Demographic and clinical data, cytology, and pathology results were entered in a database and analyzed., Results: A total of 172 patients [male to female = 1.8:1; median age, 67 years (range, 20 to 90]) were included. The diagnostic yield of EBUS cytology was 79.7% (137 of 172). Pathologic testing was available in 68% (117 of 172) and 82% (96 of 117) had a diagnostic EBUS. The diagnostic accuracy of EBUS was 91.7%. The sensitivity, specificity, positive (PPV) and negative (NPV) predictive values were 88.1% (95% confidence interval [CI], 77.3 to 94.3), 100% (95% CI, 85.9 to 100), 100% (95% CI, 92.4 to 100), and 80.6% (95% CI, 63.4 to 91.2), respectively. In 67 patients who had a suspected or biopsy-proven primary lung cancer, diagnostic yield was 86.6% and accuracy was 94.8%. In this subgroup the sensitivity, specificity, PPV, and NPV were 93% (95% CI, 76.5 to 98.9), 100% (95% CI, 69.9 to 100), 100% (95% CI, 85 to 100), and 83.3% (95% CI, 56.2 to 97.5)., Conclusions: Diagnostic performance data support the clinical usefulness of EBUS in the evaluation of patients with a radiographically abnormal mediastinum. It should be considered complementary to mediastinoscopy rather than substitutive.
- Published
- 2009
- Full Text
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47. Anatomic segmentectomy for stage I non-small cell lung cancer in the elderly.
- Author
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Kilic A, Schuchert MJ, Pettiford BL, Pennathur A, Landreneau JR, Landreneau JP, Luketich JD, and Landreneau RJ
- Subjects
- Aged, Aged, 80 and over, Female, Humans, Male, Neoplasm Staging, Retrospective Studies, Treatment Outcome, Carcinoma, Non-Small-Cell Lung pathology, Carcinoma, Non-Small-Cell Lung surgery, Lung Neoplasms pathology, Lung Neoplasms surgery, Pneumonectomy methods
- Abstract
Background: Anatomic segmentectomy for stage I non-small cell lung cancer (NSCLC) offers the potential of surgical cure with preservation of lung function. This may be of particular importance in elderly NSCLC patients with declining cardiopulmonary status and a limited life expectancy., Methods: The study compared outcomes of 78 elderly patients (aged > 75 years) with stage I NSCLC undergoing segmentectomy and 106 undergoing lobectomy for stage I NSCLC from 2002 to 2007. Primary outcome variables included perioperative morbidity and mortality, hospital course, recurrence patterns, and survival., Results: Age, gender, tumor histology, and surgical approach were similar between groups. Comorbidities were similar except for a higher incidence of chronic obstructive pulmonary disease and diabetes in segmentectomy patients. The tumors in the lobectomy group were significantly larger (3.5 vs 2.5 cm, p = 0.0001). Operative mortality was 1.3% for segmentectomy and 4.7% for lobectomy. Segmentectomy patients had fewer major complications (11.5% vs 25.5%, p = 0.02). There were no differences in median hospitalization (7 vs 6 days). The estimated overall survival at 2, 3, and 5 years was 76%, 69%, and 46% for segmentectomy patients and 68%, 59%, and 47% for lobectomy patients (p = 0.28). The 5-year disease-free survival was equivalent (segmentectomy, 49.8%; lobectomy, 45.5%; p = 0.80)., Conclusions: Anatomic segmentectomy can be performed safely in elderly patients with early-stage NSCLC. This approach is associated with reduced perioperative complications and comparable oncologic efficacy compared with lobectomy in older patients with a limited life expectancy.
- Published
- 2009
- Full Text
- View/download PDF
48. Invited commentary.
- Author
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Pennathur A and Luketich JD
- Subjects
- Antineoplastic Agents therapeutic use, Benzamides, Esophageal Neoplasms drug therapy, Esophagectomy, Follow-Up Studies, Gastrointestinal Stromal Tumors drug therapy, Humans, Imatinib Mesylate, Piperazines therapeutic use, Pyrimidines therapeutic use, Time Factors, Esophageal Neoplasms surgery, Gastrointestinal Stromal Tumors surgery, Neoplasm Recurrence, Local pathology
- Published
- 2009
- Full Text
- View/download PDF
49. Esophagectomy for T1 esophageal cancer: outcomes in 100 patients and implications for endoscopic therapy.
- Author
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Pennathur A, Farkas A, Krasinskas AM, Ferson PF, Gooding WE, Gibson MK, Schuchert MJ, Landreneau RJ, and Luketich JD
- Subjects
- Adenocarcinoma pathology, Adult, Aged, Aged, 80 and over, Carcinoma, Squamous Cell pathology, Endoscopy, Esophageal Neoplasms pathology, Female, Humans, Male, Middle Aged, Neoplasm Staging, Prognosis, Retrospective Studies, Risk Factors, Adenocarcinoma surgery, Carcinoma, Squamous Cell surgery, Esophageal Neoplasms surgery, Esophagectomy
- Abstract
Objectives: Esophagectomy is the standard treatment for T1 esophageal cancer (EC). Interest in endoscopic therapies, particularly for T1 EC, is increasing. We evaluated the long-term outcomes after esophagectomy and examined the pathologic features of T1 cancer to determine the suitability for potential endoscopic therapy., Methods: We reviewed the outcomes of esophagectomy in 100 consecutive patients with T1 EC. The primary end points studied were overall survival (OS) and disease-free survival (DFS). In addition to detailed pathology review, we evaluated prognostic variables associated with survival., Results: Esophagectomy was performed in 100 patients (79 men, 21 women; median age, 68 years) for T1 EC, comprising adenocarcinoma, 91; squamous, 9; intramucosal (T1a), 29; and submucosal (T1b), 71. The 30-day mortality was 0%. Resection margins were microscopically negative in 99 patients (99%). N1 disease was present in 21 (T1a, 2 of 29 [7%]; T1b, 19 of 71 [27%]), associated high-grade dysplasia in 64 (64%), and angiolymphatic invasion in 19 (19%). At a median follow-up of 66 months, estimated 5-year OS was 62% and 3-year DFS was 80% for all patients (including N1). Nodal status and tumor size were significantly associated with OS and DFS, respectively., Conclusions: Esophagectomy can be performed safely in patients with T1 EC with good long-term results. Many patients with T1 EC have several risk factors that may preclude adequate treatment with endoscopic therapy. Further prospective studies are required to evaluate endoscopic therapies. Esophagectomy should continue to remain the standard treatment in patients with T1 EC.
- Published
- 2009
- Full Text
- View/download PDF
50. Radiofrequency ablation for the treatment of pulmonary metastases.
- Author
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Pennathur A, Abbas G, Qureshi I, Schuchert MJ, Wang Y, Gilbert S, Landreneau RJ, and Luketich JD
- Subjects
- Adult, Aged, Aged, 80 and over, Female, Humans, Lung Neoplasms mortality, Lung Neoplasms secondary, Male, Middle Aged, Patient Selection, Pneumonectomy, Prognosis, Retrospective Studies, Survival Analysis, Treatment Outcome, Catheter Ablation, Lung Neoplasms surgery
- Abstract
Objectives: Surgical resection is the preferred treatment in selected patients with pulmonary metastases. In high-risk patients, radiofrequency ablation (RFA) may offer an alternative option. RFA may be used alone or combined with surgical resection as a lung parenchymal-sparing approach. Our objectives were to evaluate the intermediate term outcomes after RFA and to determine the prognostic variables associated with outcome in patients with pulmonary metastases., Methods: Thoracic surgeons evaluated and performed RFA under computed tomography (CT) guidance or combined with surgical resection. Patients were monitored in the thoracic surgery clinic for recurrence and survival., Results: Twenty-two patients (10 men, 12 women; median age, 63 years [range, 37 to 88]) underwent RFA. The primary cancer was colorectal in 9 (41%), renal in 2 (9%), sarcoma in 4 (18%), and other in 7 (32%). CT-guided RFA was the sole treatment in 17 patients (77%) and combined with surgical resection in 5 (23%). No procedurally related deaths occurred. At a mean follow-up of 27 months (range, 13.3 to 53.6 months), 9 patients are alive. The median survival was 29 months (95% confidence interval, 9.1 to 33.8). Lesion size was an important prognostic variable associated with overall and disease-free survival (p < 0.05)., Conclusions: RFA is safe in this group of pulmonary metastases patients, with reasonable results. Surgical resection remains the standard for resectable patients, but RFA offers an alternative in selected patients or may be used as a parenchymal-sparing approach in combination with surgical resection in selected patients.
- Published
- 2009
- Full Text
- View/download PDF
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