90 results on '"Conejo, E."'
Search Results
2. WETLANDS CONSTRUÍDOS COMO SUMIDOUROS DE CARBONO OU COMO FONTES DE EMISSÃO – UMA REVISÃO
- Author
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Gabriela Oliveira Valença, Paulo Belli Filho, Dayane Dall’Ago Conejo e Silva, and Rodrigo de Almeida Mohedano
- Subjects
Wetland construído ,Gases do efeito estufa ,mudanças climáticas ,Architecture ,NA1-9428 ,Engineering (General). Civil engineering (General) ,TA1-2040 - Abstract
Diante do cenário de aquecimento global, diversas pesquisas sobre remoção de carbono como forma de mitigar os efeitos das mudanças climáticas vêm sendo realizadas. O uso de wetlands construídos para tratamento de águas residuais é conhecido, entretanto a quantidade de estudos sobre o sequestro de carbono desse sistema ainda é limitada. Dessa forma, a revisão sistemática e de literatura teve como objetivo expor as características dos wetlands construídos em relação às emissões de Gases do Efeito Estufa. As bases utilizadas foram Scopus, Springer e Google Scholar e os termos selecionados estavam relacionados aos wetlands construídos e aos gases. Concluiu-se que o wetland construído subsuperficial horizontal tem o potencial de se tornar sumidouro de carbono, por conta do carbono retido nas plantas, e pode emitir menos N2O que o WC de fluxo vertical; quanto à emissão de CH4 é importante conhecer a espécie de planta adotada e o tipo de WC por conta da influência nas emissões de metano.
- Published
- 2023
3. WETLANDS CONSTRUÍDOS COMO SUMIDOUROS DE CARBONO OU COMO FONTES DE EMISSÃO – UMA REVISÃO
- Author
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Oliveira Valença, Gabriela, primary, Belli Filho, Paulo, additional, Dall’Ago Conejo e Silva, Dayane, additional, and De Almeida Mohedano, Rodrigo, additional
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- 2023
- Full Text
- View/download PDF
4. 262P Niraparib plus aromatase inhibitors (AI) for germinal mutated BRCA1/2 (gBRCAm) or homologous recombination-deficient (HRd), hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer (ABC): LUZERN interim analysis
- Author
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Pimentel, I., primary, Lema Roso, L., additional, Ramos Vazquez, M., additional, García Saenz, J.Á., additional, Palacios-Ozores, P., additional, De la Haba Rodriguez, J., additional, Blanch, S., additional, Prat, A., additional, Ales Martínez, J.E., additional, Alba Conejo, E., additional, Balmaña, J., additional, Perez Garcia, J.M., additional, Sampayo-Cordero, M., additional, Malfettone, A., additional, Cortés, J., additional, and Llombart Cussac, A., additional
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- 2022
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5. 1721P Hereditary component of HER2-positive breast cancer
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Iglesias Campos, M., primary, Jimena Márquez, A., additional, Peralta Linero, R.J., additional, and Alba Conejo, E., additional
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- 2022
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6. Erythropoietin pharmacology
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Jurado García, J. M., Torres Sánchez, E., Olmos Hidalgo, D., and Alba Conejo, E.
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- 2007
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7. 2204P Clinical predictors and inflammatory markers for malignant pleural mesothelioma prognosis: A retrospective study in a Spanish Medical Oncology Unit
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Guardamagna, M., Gonzalez, B. Villaescusa, Dolores, M.R. María, Gonzalez, E. Zamorano, Garcia, I. Ramos, Ruiz, A. Mesas, Perez, J.M. Trigo, Cantero, A., Calderon, V. Gutierrez, García, J.M. Jurado, Dominguez, A. Rueda, Mongil, R., Arrabal, R., Conejo, E. Alba, Dols, M. Cobo, and Montanez, J.C. Benitez
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- 2023
- Full Text
- View/download PDF
8. 73TiP SOLTI1710 PROMETEO II: Palbociclib in combination with letrozole in hormone receptor-positive (HR+)/HER2-negative residual disease after standard neoadjuvant chemotherapy (NAC)
- Author
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Ciruelos, E., primary, Salvador Bofill, F.J., additional, Perello Martorell, A., additional, Conejo, E. Alba, additional, González-Farré, X., additional, Palacios-Ozores, P., additional, Merino, M., additional, Villagrasa, P., additional, Navarro, E. Vila, additional, Pascual, T., additional, Prat, A., additional, and Pernas Simon, S., additional
- Published
- 2021
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9. 91O Pooled analysis of patient (pt)-reported outcomes (PROs) in the MONALEESA (ML)-2, -3, and -7 trials: Additional results and key subgroup findings
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Fasching, P.A., primary, Bardia, A., additional, Nusch, A., additional, Jerusalem, G., additional, Chan, A., additional, El Saghir, N.S., additional, Alba Conejo, E., additional, Im, S-A., additional, Janni, W., additional, Chandiwana, D., additional, Lanoue, B.R., additional, Thuerigen, A., additional, Gu, E., additional, and Harbeck, N., additional
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- 2021
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10. A Neural Network Based Model for Prognosis of Early Breast Cancer
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Gómez-Ruiz, J.A., Jerez-Aragonés, J.M., Muñoz-Pérez, J., and Alba-Conejo, E.
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- 2004
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11. 3D Gas Concentration Mapping of Active Volcanoes using Mass Spectrometry
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Diaz, J. A, Arkin, C. R, Griffin, T. P, Conejo, E, Heinrich, K, Soto, C, Bogantes, L, Naylor, G. R, Curley, C, Floyd, D, and Gomez, O
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Earth Resources And Remote Sensing - Published
- 2005
12. Portable Mass Spectrometer System for in-situ Environmental Gas Monitoring
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Conejo, E, Griffin, T. P, Diaz, J. A, Arkin, C. R, Soto, C, Naylor, G. R, Curley, C, and Floyd, D
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Instrumentation And Photography - Abstract
A system developed by NASA has been used for monitoring air quality around different locations. The system was designed for aircraft applications but has proven to be very useful as a portable gas analyzer. The system has been used to monitor air quality around volcanoes, cities, and the surrounding areas. The transport of the system has been via aircraft, car, and hand carried.
- Published
- 2005
13. Duration of response and tumor shrinkage with first-line ribociclib + letrozole in postmenopausal women with HR+, HER2– ABC
- Author
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Janni, W., primary, Alba Conejo, E., additional, Bachelot, T., additional, Diab, S., additional, Gil-Gil, M., additional, Beck, T.J., additional, Ryvo, L., additional, López, R., additional, Tsai, M., additional, Esteva, F.J., additional, Zamora Aunon, M.P., additional, Kral, Z., additional, Ward, P., additional, Richards, P., additional, Pluard, T.J., additional, Sutradhar, S., additional, Miller, M., additional, and Campone, M., additional
- Published
- 2017
- Full Text
- View/download PDF
14. Phase III evaluating the addition of fulvestrant (F) to anastrozol (A) as adjuvant therapy in postmenopausal women with hormone receptor positive HER2 negative (HR+/HER2-) early breast cancer (EBC): Results from the GEICAM/2006-10 study
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Ruiz-Borrego, M., primary, Martin Jimenez, M., additional, Ruiz, A., additional, Lluch, A., additional, Ramos, M., additional, Cruz Jurado, J., additional, Baena-Canada, J.M., additional, Cirauqui, B., additional, Rodriguez-Lescure, A., additional, Alba Conejo, E., additional, Martínez Jañez, N., additional, Muñoz, M., additional, Antolin, S., additional, Álvarez López, I., additional, Del Barco, S., additional, Garcia-Estevez, L., additional, Chacon Lopez-Muniz, J.I., additional, Anton Torres, A., additional, and Carrasco, E., additional
- Published
- 2017
- Full Text
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15. Prognostic significance of immunohistochemical subtyping and PAM50 intrinsic subtypes in male breast cancer (MaBC)
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Alvarez, M., primary, Sanchez-Muñoz, A., additional, Santonja, A., additional, Fernández, Y. Plata, additional, Miramón, J., additional, Pedrinaci, I. Zarcos, additional, Llacer, C., additional, de Luque, V., additional, León, M.J. Lozano, additional, Jerez, J.M., additional, Villa, L. Pérez, additional, Lavado, R., additional, Ramirez, C., additional, Jiménez, A., additional, Rodrigo, I., additional, García, E., additional, Vicioso, L., additional, and Conejo, E. Alba, additional
- Published
- 2016
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16. Luminal androgen receptor role and pathological complete response rate to neoadjuvant chemotherapy in triple negative breast cancer
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Chica-Parrado, M.R., primary, Santonja, A., additional, Lluch-Hernandez, A., additional, Albanell, J., additional, Sanchez-Muñoz, A., additional, Chacón, I., additional, Calvo, L., additional, Sanchez-Rovira, P., additional, De Haba, J.l.a., additional, Vicioso, L., additional, Martin, M., additional, Plazaola, A., additional, Prat, A., additional, Ribelles, N., additional, Sánchez-Aragó, M., additional, Jerez, J.M., additional, Escudero, M.J., additional, Caballero, R., additional, Carrasco, E., additional, and Conejo, E. Alba, additional
- Published
- 2016
- Full Text
- View/download PDF
17. Gestational breast cancer: distinctive molecular and clinico-epidemiological features. GEICAM/2012-03 study
- Author
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Haba, Jdela, primary, Ruiz, A., additional, Pollan, M., additional, Prat, A., additional, Rojo, F., additional, Martin, M., additional, Conejo, E. Alba, additional, Perez-Fidalgo, J.A., additional, Gavilá, J., additional, Morales, C., additional, Navarro, B., additional, Hernández-Blanquisett, A., additional, Porras, I., additional, Rodriguez-Lescure, A., additional, Jiménez-Rodríguez, B., additional, Martín, N., additional, Pérez-Ramos, L., additional, Caballero, R., additional, Carrasco, E., additional, and Lluch-Hernandez, A., additional
- Published
- 2016
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- View/download PDF
18. Device for automatic evaluation of biomaterials micro-leakage by gas permeability
- Author
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Chavarria-Bolaños, D., primary, Sánchez, A., additional, Conejo, E., additional, and Pozos-Guillén, A., additional
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- 2016
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19. EP-1319: Application ACOSOG Z0011: no axillary dissection in women with invasive breast cancer and sentinel node metastasis
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García Ríos, I., primary, Sanz-Viedma, S., additional, Scholz, V., additional, Ribelles, N., additional, Vicioso, L., additional, Soler, C., additional, Jimenez Hoyuela, J.M., additional, Roman Jobacho, A., additional, Gomez-Millan, J., additional, Alba Conejo, E., additional, and Medina Carmona, J.A., additional
- Published
- 2015
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- View/download PDF
20. 245PD - Duration of response and tumor shrinkage with first-line ribociclib + letrozole in postmenopausal women with HR+, HER2– ABC
- Author
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Janni, W., Alba Conejo, E., Bachelot, T., Diab, S., Gil-Gil, M., Beck, T.J., Ryvo, L., López, R., Tsai, M., Esteva, F.J., Zamora Aunon, M.P., Kral, Z., Ward, P., Richards, P., Pluard, T.J., Sutradhar, S., Miller, M., and Campone, M.
- Published
- 2017
- Full Text
- View/download PDF
21. 148O - Phase III evaluating the addition of fulvestrant (F) to anastrozol (A) as adjuvant therapy in postmenopausal women with hormone receptor positive HER2 negative (HR+/HER2-) early breast cancer (EBC): Results from the GEICAM/2006-10 study
- Author
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Ruiz-Borrego, M., Martin Jimenez, M., Ruiz, A., Lluch, A., Ramos, M., Cruz Jurado, J., Baena-Canada, J.M., Cirauqui, B., Rodriguez-Lescure, A., Alba Conejo, E., Martínez Jañez, N., Muñoz, M., Antolin, S., Álvarez López, I., Del Barco, S., Garcia-Estevez, L., Chacon Lopez-Muniz, J.I., Anton Torres, A., and Carrasco, E.
- Published
- 2017
- Full Text
- View/download PDF
22. Carcinoide de células globoides del apéndice: Varón de 52 años con apendicitis aguda
- Author
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Trujillo Vilchez, R., Pérez Martín, D., Quero Blanco, C., Márquez Aragonés, A., Funez Liebana, R., Moya Donoso, F. J., and Alba Conejo, E.
- Subjects
endocrine system ,Small-bowel neoplasms ,Adenocarcinoid ,Adenocarcinoide ,endocrine system diseases ,Goblet cell carcinoid ,Carcinoide de células globoides ,Apéndice ,Appendix ,digestive system ,neoplasms ,digestive system diseases ,Neoplasias de intestino delgado - Abstract
Goblet cell carcinoid, also variably known as adenocarcinoid, mucinous carcinoid, and crypt cell carcinoma, is a rare neoplasm with distinct histological and clinical features. We review the management of goblet cell carcinoid of the appendix using an illustrative case report. El carcinoide de células globoides, también denominado adenocarcinoide, carcinoma mucinoso, y carcinoma de células de la cripta, es una rara neoplasia con características específicas clínicas y patológicas. Revisamos el manejo del carcinoide de células globoides del apéndice aprovechando la presentación de un caso clínico ilustrativo.
- Published
- 2007
23. 289P - Prognostic significance of immunohistochemical subtyping and PAM50 intrinsic subtypes in male breast cancer (MaBC)
- Author
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Alvarez, M., Sanchez-Muñoz, A., Santonja, A., Fernández, Y. Plata, Miramón, J., Pedrinaci, I. Zarcos, Llacer, C., de Luque, V., León, M.J. Lozano, Jerez, J.M., Villa, L. Pérez, Lavado, R., Ramirez, C., Jiménez, A., Rodrigo, I., García, E., Vicioso, L., and Conejo, E. Alba
- Published
- 2016
- Full Text
- View/download PDF
24. 187P - Luminal androgen receptor role and pathological complete response rate to neoadjuvant chemotherapy in triple negative breast cancer
- Author
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Chica-Parrado, M.R., Santonja, A., Lluch-Hernandez, A., Albanell, J., Sanchez-Muñoz, A., Chacón, I., Calvo, L., Sanchez-Rovira, P., De Haba, J.l.a., Vicioso, L., Martin, M., Plazaola, A., Prat, A., Ribelles, N., Sánchez-Aragó, M., Jerez, J.M., Escudero, M.J., Caballero, R., Carrasco, E., and Conejo, E. Alba
- Published
- 2016
- Full Text
- View/download PDF
25. 154PD - Gestational breast cancer: distinctive molecular and clinico-epidemiological features. GEICAM/2012-03 study
- Author
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Haba, Jdela, Ruiz, A., Pollan, M., Prat, A., Rojo, F., Martin, M., Conejo, E. Alba, Perez-Fidalgo, J.A., Gavilá, J., Morales, C., Navarro, B., Hernández-Blanquisett, A., Porras, I., Rodriguez-Lescure, A., Jiménez-Rodríguez, B., Martín, N., Pérez-Ramos, L., Caballero, R., Carrasco, E., and Lluch-Hernandez, A.
- Published
- 2016
- Full Text
- View/download PDF
26. Randomised, phase II trial comparing oral capecitabine (Xeloda) with paclitaxel in patients with metastatic/advanced breast cancer pretreated with anthracyclines.
- Author
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Talbot, D.C., Moiseyenko, V., Van Belle, S., O'Reilly, S.M., Conejo, E. Alba, Ackland, S., Eisenberg, P., Melnychuk, D., Pienkowski, T., Burger, H.-U., Laws, S., Osterwalder, B., and Alba Conejo, E
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BREAST cancer treatment ,ANTHRACYCLINES ,FLUOROPYRIMIDINES ,PACLITAXEL ,ANTINEOPLASTIC antibiotics ,ORAL drug administration ,ANTINEOPLASTIC agents ,DEOXYCYTIDINE ,METASTASIS ,ANTIMETABOLITES ,FLUOROURACIL ,TREATMENT effectiveness ,RANDOMIZED controlled trials ,STATISTICAL sampling ,BREAST tumors ,PHARMACODYNAMICS - Abstract
Capecitabine, an oral fluoropyrimidine carbamate, was designed to generate 5-fluorouracil preferentially at the tumour site. This randomised, phase II trial evaluated the efficacy and safety of capecitabine or paclitaxel in patients with anthracycline-pretreated metastatic breast cancer. Outpatients with locally advanced and/or metastatic breast cancer whose disease was unresponsive or resistant to anthracycline therapy were randomised to 3-week cycles of intermittent oral capecitabine (1255 mg m(-2) twice daily, days 1-14, (22 patients)) or a reference arm of i.v. paclitaxel (175 mg m(-2), (20 patients)). Two additional patients were initially randomised to continuous capecitabine 666 mg m(-2) twice daily, but this arm was closed following selection of the intermittent schedule for further development. Overall response rate was 36% (95% CI 17-59%) with capecitabine (including three complete responses) and 26% (95% CI 9-51%) with paclitaxel (no complete responses). Median time to disease progression was similar in the two treatment groups (3.0 months with capecitabine, 3.1 months with paclitaxel), as was overall survival (7.6 and 9.4 months, respectively). Paclitaxel was associated with more alopecia, peripheral neuropathy, myalgia and neutropenia, whereas typical capecitabine-related adverse events were diarrhoea, vomiting and hand-foot syndrome. Twenty-three per cent of capecitabine-treated patients and 16% of paclitaxel-treated patients achieved a > or =10% improvement in Karnofsky Performance Status. Oral capecitabine is active in anthracycline-pretreated advanced/metastatic breast cancer and has a favourable safety profile. Furthermore, capecitabine provides a convenient, patient-orientated therapy. [ABSTRACT FROM AUTHOR]
- Published
- 2002
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27. Bevacizumab–Capecitabine (BEV–CAP) After Initial 1st-Line Bevacizumab–Docetaxel (BEV–DOC) in Patients (PTS) With HER2-Negative Metastatic Breast Cancer (MBC): Safety Analysis of the IMELDA Trial
- Author
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Gligorov, J., primary, Alba-Conejo, E., additional, Bines, J., additional, Cortes, P.A., additional, Doval, D.C., additional, Jiang, Z., additional, Freudensprung, U., additional, and Mustacchi, G., additional
- Published
- 2012
- Full Text
- View/download PDF
28. Mamasteam: Bevacizumab (BVZ) in the Treatment of Breast Cancer in Advanced Lines of Treatment, a New Model for the Assessment of Activity in Advanced Cancer
- Author
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De Rodriguez, J. La Haba, primary, Martin, A. Gonzalez, additional, Rodriguez-Lescure, A., additional, Pulido, G., additional, Sanchez-MuÑoz, A., additional, Marquez, R., additional, Rueño, M. Guirado, additional, Castro, D. Torrejon, additional, Alba-Conejo, E., additional, and Cortes, J., additional
- Published
- 2012
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29. Proliferation Determined by KI67 Marker Defines Pathological Complete Response in a Dose-Dense Neoadjuvant Chemotherapy Schedule in Locally Advanced Breast Cancer Patients
- Author
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Fernandez, M.Y. Plata, primary, Sanchez-Muñoz, A., additional, Jaén-Morago, A., additional, Lomas-Garrido, M., additional, Fernández, M., additional, Llacer, C., additional, Ribelles, N., additional, Alba-Conejo, E., additional, and Sánchez-Rovira, P., additional
- Published
- 2012
- Full Text
- View/download PDF
30. Goblet Cell Carcinoid of the appendix: a 52 years old male with acute appendicitis
- Author
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Trujillo Vilchez, R., primary, Pérez Martín, D., additional, Quero Blanco, C., additional, Márquez Aragonés, A., additional, Funez Liebana, R., additional, Moya Donoso, F. J., additional, and Alba Conejo, E., additional
- Published
- 2007
- Full Text
- View/download PDF
31. Validation of a Complex Permittivity Meter for Porous Media Operating Between 1 and 20 MHz.
- Author
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Bexi, I., Chavanne, X., Conejo, E., and Frangi, J-P
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POROUS materials ,ELECTRIC insulators & insulation ,CIRCUIT elements ,ELECTRIC resistance ,ELECTRIC impedance ,ELECTRIC displacement - Abstract
This paper describes the procedure to qualify an admittance meter as a permittivity meter and a conductivity meter σsensor through validation with liquids over a range of relative permittivity εr values from 1 to 80 and with operating frequencies f between 1 and 20 MHz. The sensor is a capacitor which consists of two parallel cylinders of 10-cm typical dimension. A circuit-based model of the sensor was previously calibrated against accurate electronic components. A discrepancy of 10% is found between the calibration with components and the validation with liquids. All potential errors have been carefully examined: parasitic impedances of the electronic circuit and leads, modifications of liquid permittivity εrliq due to temperature influence, water contamination or relaxation effects, and possible fringing effects with the help of numeric simulations. Forty percent of the discrepancy results from the finite dimensions of the liquid-filled recipient. The fringing effects due to insulating rings at each end of the capacitor seem to be discarded. The analysis of the uncertainty on εrsensor and σsensor shows a relative uncertainty of 3%-5% due in large part to the numerical acquisition of high frequency. [ABSTRACT FROM PUBLISHER]
- Published
- 2012
- Full Text
- View/download PDF
32. Initialization of adjuvant hormonal treatment for breast cancer.
- Author
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Martínez Guisado, Antonia, Sánchez Muñoz, Alfonso, Cabeza Lomas Garrido, María, Ruíz Borrego, Manuel, Bayo Calero, Juan, Toro Salas, Rubén, González Mancha, R., Haba Rodríguez, Juan, Alba Conejo, Emilio, Martínez Guisado, A, Sánchez Muñoz, A, de la Cabeza Lomas Garrido, M, Ruíz Borrego, M, Bayo Calero, J, de Toro Salas, R, González Mancha, R, de la Haba Rodríguez, J, and Alba Conejo, E
- Abstract
The introduction of aromatase inhibitors (AI) has resulted in practice change approaches in the treatment of early breast cancer. In this paper, we analyze the most relevant studies including the ATAC, BIG 1-98, TEAM, MA-17, NSABP B-33, and ABSCG-6 studies. Postmenopausal patients with hormone receptor-positive early breast cancer should be treated with AI for 5 years. For patients who have been initiated with tamoxifen (TAM), switching to an AI to complete 5 years of treatment is also recommended. The results of the extended adjuvant therapy studies recommend the use of an AI (anastrozole, letrozole, or exemestane) after the completion of standard TAM treatment. With regards to premenopausal women, TAM is the recommended adjuvant hormonal treatment for pre- and perimenopausal women. There is no indication for the use of AI in these subgroups of patients. Finally, determination of CYP 2D6 polymorphisms could be considered when choosing the best adjuvant hormonal treatment option. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF
33. 400 - Mamasteam: Bevacizumab (BVZ) in the Treatment of Breast Cancer in Advanced Lines of Treatment, a New Model for the Assessment of Activity in Advanced Cancer
- Author
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De Rodriguez, J. La Haba, Martin, A. Gonzalez, Rodriguez-Lescure, A., Pulido, G., Sanchez-MuÑoz, A., Marquez, R., Rueño, M. Guirado, Castro, D. Torrejon, Alba-Conejo, E., and Cortes, J.
- Published
- 2012
- Full Text
- View/download PDF
34. 356P - Bevacizumab–Capecitabine (BEV–CAP) After Initial 1st-Line Bevacizumab–Docetaxel (BEV–DOC) in Patients (PTS) With HER2-Negative Metastatic Breast Cancer (MBC): Safety Analysis of the IMELDA Trial
- Author
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Gligorov, J., Alba-Conejo, E., Bines, J., Cortes, P.A., Doval, D.C., Jiang, Z., Freudensprung, U., and Mustacchi, G.
- Published
- 2012
- Full Text
- View/download PDF
35. 268P - Proliferation Determined by KI67 Marker Defines Pathological Complete Response in a Dose-Dense Neoadjuvant Chemotherapy Schedule in Locally Advanced Breast Cancer Patients
- Author
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Fernandez, M.Y. Plata, Sanchez-Muñoz, A., Jaén-Morago, A., Lomas-Garrido, M., Fernández, M., Llacer, C., Ribelles, N., Alba-Conejo, E., and Sánchez-Rovira, P.
- Published
- 2012
- Full Text
- View/download PDF
36. Lean adolescents with increased risk for metabolic syndrome
- Author
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Molero-Conejo, E., Morales, L. M., Fernández, V., Raleigh, X., Gómez, M. E., Semprún-Fereira, M., Campos, G., and Elena Ryder
- Subjects
dieta ,insulin resistance ,Insulina ,insulino resistencia ,índice de masa corporal ,Insulin ,physical activity ,adolescentes ,body mass index ,adolescents ,actividad física ,diet - Abstract
SUMMARY. The aim of the present study was to determine in adolescents the relationship between insulin levels and body mass index (BMI), body fat distribution, diet, life style and lipid profile. We studied 167 adolescents (68 boys and 99 girls) whose ages ranged from 14 to 17 years. A detailed medical (including pubertal stage) and nutritional record was obtained from each subject. Biochemical measurements included fasting serum insulin, glucose, total cholesterol (TC), triglycerides (Tg), HDL-C, LDL-C and VLDL-C. HOMA insulin resistance (IR) and HOMA beta -cell function (beta -cell) were calculated. Insulin levels were over 84 pmol/L (cut off normal value in our lab) in 56% of the boys and 43% of the girls. Thirty-seven percent of lean adolescents whose BMI was 21.5 ± 1.9 kg/m² presented higher fasting insulin levels, HOMA IR, Tg, systolic (SBP) and diastolic blood pressure (DBP) values when compared to a lean normoinsulinemic group. Insulin levels were correlated (p< 0.01) with body mass index. Both boys and girls in the highest BMI quartile (BMI > 24 kg/m²) had significantly higher serum insulin, HOMA beta -cell, and Tg levels, and the lowest HDL-C levels. A high-energy intake rich in saturated fat and low physical activity were found in this lean but metabolically altered adolescents. We conclude that even with a BMI as low as 21 kg/m² an inappropriate diet and low physical activity might be responsible for the high insulin levels and dislipidemias in adolescents. RESUMEN. El objetivo del presente estudio fue determinar la relación entre los niveles de insulina y el Indice de Masa Corporal (IMC), distribución de grasa corporal, dieta, estilo de vida y perfil lipídico en adolescentes. A cada adolescente se la realizó una historia clínica detallada (incluyendo estadío puberal), además de una encuesta nutricional. Dentro de los parámetros bioquímicos se determinaron en suero los niveles de glicemia e insulina basal, colesterol total (CT), triglicéridos (TG), HDL-C, LDL-C, y VLDL-C. Se calcularon el HOMA-IR, y el HOMA-ß-cell. Se encontró que el 56% de los varones y el 43% de las hembras tenía valores de insulina > 84pmol/L (valor de referencia para nuestro laboratorio). Un 37% de los adolescentes delgados, con un IMC promedio de 21,5 ± 1,9 kg/m², presentó niveles elevados de insulina, HOMA-IR, TG, presión arterial sistólica y diastólica comparados con el grupo de adolescentes delgados normoinsulinémicos. Se encontró una correlación positiva y significativa (p< 0,01) entre los niveles de insulina y el IMC. Tanto los varones como las hembras ubicados en los cuartiles más altos de IMC (IMC>24 kg/m² ), tenian niveles significativamente más altos de insulina, HOMA- ßcell y TG, acompañados de niveles más bajos de HDL-C. Una alta ingesta de energía rica en grasa saturadas y una baja actividad física, se encontraron en estos adolescentes delgados pero metabólicamente alterados. En conclusión, niveles tan bajos de IMC como 21 kg/m², una dieta inapropiada y una baja actividad física pueden ser responsables de los altos niveles de insulina y dislipidemias en los adolescentes.
37. Lack of evidence for KRAS oncogenic mutations in triple-negative breast cancer
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Elena Gallego, Vanessa de Luque, Nuria Ribelles, Luis Vicioso, José Manuel Lozano, Emilio Alba, Alfonso Sánchez-Muñoz, Luis G. Perez-Rivas, [Sánchez-Muñoz,A, Ribelles Entrena,N, Alba Conejo,E] Servicio de Oncología Médica, Hospital Universitario Virgen de la Victoria, Málaga, España. [Gallego Domínguez,E, Vicioso Recio,L] Servicio de Anatomía Patológica, Hospital Universitario Virgen de la Victoria, Málaga, España. [Sánchez-Muñoz,A, Gallego Domínguez,EM, Luque,V de, Pérez-Rivas,LG, Vicioso Recio,L, Lozano Castro,J, Alba Conejo,E] Laboratorio de Investigación Biomédica (LIB-IMABIS), Hospital Universitario Virgen de la Victoria, Málaga, España. [Lozano Castro,J] Dpto. de Biología Molecular y Bioquímica, Facultad de Ciencias, Universidad de Málaga, España., and This work was supported by Fondo de Investigaciones Sanitarias grant PI081797 (to E. A.) and Ministerio de Ciencia e Innovación grant BFU2007-66100 (to J. L.).
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Cancer Research ,Chemicals and Drugs::Chemical Actions and Uses::Pharmacologic Actions::Molecular Mechanisms of Pharmacological Action::Enzyme Inhibitors::Protein Kinase Inhibitors [Medical Subject Headings] ,Colorectal cancer ,Receptor, ErbB-2 ,KRAS protein, human ,Marcadores tumorales ,DNA Mutational Analysis ,medicine.disease_cause ,Chemicals and Drugs::Enzymes and Coenzymes::Enzymes::Hydrolases::Acid Anhydride Hydrolases::GTP Phosphohydrolases::GTP-Binding Proteins::Monomeric GTP-Binding Proteins::ras Proteins [Medical Subject Headings] ,Polymerase Chain Reaction ,Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings] ,Chemicals and Drugs::Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases::Receptor Protein-Tyrosine Kinases::Receptor, erbB-2 [Medical Subject Headings] ,KRT5 protein, human ,Surgical oncology ,Análisis Mutacional de ADN ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Sequence Analysis::Sequence Analysis, DNA::DNA Mutational Analysis [Medical Subject Headings] ,Triple-negative breast cancer ,EGFR inhibitors ,Cetuximab ,Queratina-5 ,Marcadores biológicos de tumor ,Proteínas ras ,Diseases::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Glandular and Epithelial::Neoplasms, Basal Cell [Medical Subject Headings] ,Queratina-6 ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Immunohistochemistry ,Proteínas Proto-Oncogénicas ,Chemicals and Drugs::Macromolecular Substances::Polymers::Biopolymers::Intermediate Filament Proteins::Keratins::Keratins, Type II::Keratin-5 [Medical Subject Headings] ,ErbB Receptors ,Gene Expression Regulation, Neoplastic ,Oncology ,Receptors, Estrogen ,Neoplasias de la mama ,Inhibidores de las Proteína Quinasas ,Health Care::Health Services Administration::Patient Care Management::Patient Selection [Medical Subject Headings] ,Neoplasias vasocelulares ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Cytological Techniques::Histocytochemistry::Immunohistochemistry [Medical Subject Headings] ,Female ,KRAS ,Chemicals and Drugs::Biological Factors::Biological Markers::Tumor Markers, Biological [Medical Subject Headings] ,Receptors, Progesterone ,medicine.drug ,Research Article ,Phenomena and Processes::Genetic Phenomena::Genetic Variation::Mutation [Medical Subject Headings] ,Receptores estrogénicos ,Selección de pacientes ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::DNA-Binding Proteins::Receptors, Cytoplasmic and Nuclear::Receptors, Steroid::Receptors, Progesterone [Medical Subject Headings] ,Breast Neoplasms ,Receptores de progesterona ,Biology ,lcsh:RC254-282 ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::DNA-Binding Proteins::Receptors, Cytoplasmic and Nuclear::Receptors, Steroid::Receptors, Estrogen [Medical Subject Headings] ,Proto-Oncogene Proteins p21(ras) ,EGFR protein, human ,Breast cancer ,Chemicals and Drugs::Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases::Receptor Protein-Tyrosine Kinases::Receptor, Epidermal Growth Factor [Medical Subject Headings] ,Proto-Oncogene Proteins ,medicine ,Genetics ,Biomarkers, Tumor ,Panitumumab ,Humans ,Protein Kinase Inhibitors ,Diseases::Neoplasms::Neoplasms by Site::Breast Neoplasms [Medical Subject Headings] ,Chemicals and Drugs::Macromolecular Substances::Polymers::Biopolymers::Intermediate Filament Proteins::Keratins::Keratins, Type II::Keratin-6 [Medical Subject Headings] ,Neoplasms, Basal Cell ,Mutación ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Neoplasm Proteins::Oncogene Proteins::Proto-Oncogene Proteins [Medical Subject Headings] ,Patient Selection ,Keratin-6 ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Nucleic Acid Amplification Techniques::Polymerase Chain Reaction [Medical Subject Headings] ,ERBB2 protein, human ,medicine.disease ,Phenomena and Processes::Genetic Phenomena::Genetic Processes::Gene Expression Regulation::Gene Expression Regulation, Neoplastic [Medical Subject Headings] ,Receptor del Factor de Crecimiento Epidérmico ,Check Tags::Female [Medical Subject Headings] ,Mutation ,Reacción en Cadena de la Polimerasa ,Cancer research ,ras Proteins ,Keratin-5 ,Regulación Neoplásica de la Expresión Génica ,Inmunohistoquímica - Abstract
Background Mutational analysis of the KRAS gene has recently been established as a complementary in vitro diagnostic tool for the identification of patients with colorectal cancer who will not benefit from anti-epidermal growth factor receptor (EGFR) therapies. Assessment of the mutation status of KRAS might also be of potential relevance in other EGFR-overexpressing tumors, such as those occurring in breast cancer. Although KRAS is mutated in only a minor fraction of breast tumors (5%), about 60% of the basal-like subtype express EGFR and, therefore could be targeted by EGFR inhibitors. We aimed to study the mutation frequency of KRAS in that subtype of breast tumors to provide a molecular basis for the evaluation of anti-EGFR therapies. Methods Total, genomic DNA was obtained from a group of 35 formalin-fixed paraffin-embedded, triple-negative breast tumor samples. Among these, 77.1% (27/35) were defined as basal-like by immunostaining specific for the established surrogate markers cytokeratin (CK) 5/6 and/or EGFR. KRAS mutational status was determined in the purified DNA samples by Real Time (RT)-PCR using primers specific for the detection of wild-type KRAS or the following seven oncogenic somatic mutations: Gly12Ala, Gly12Asp, Gly12Arg, Gly12Cys, Gly12Ser, Gly12Val and Gly13Asp. Results We found no evidence of KRAS oncogenic mutations in all analyzed tumors. Conclusions This study indicates that KRAS mutations are very infrequent in triple-negative breast tumors and that EGFR inhibitors may be of potential benefit in the treatment of basal-like breast tumors, which overexpress EGFR in about 60% of all cases.
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- 2009
38. Randomized Phase 3 Trial of Fluorouracil, Epirubicin, and Cyclophosphamide Alone or Followed by Paclitaxel for Early Breast Cancer
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Miguel, Martín, Alvaro, Rodríguez-Lescure, Amparo, Ruiz, Emilio, Alba, Lourdes, Calvo, Manuel, Ruiz-Borrego, Blanca, Munárriz, César A, Rodríguez, Carmen, Crespo, Enrique, de Alava, José Antonio, López García-Asenjo, María Dolores, Guitián, Sergio, Almenar, Jesús Fernando, González-Palacios, Francisco, Vera, José, Palacios, Manuel, Ramos, Jose Manuel, Gracia Marco, Ana, Lluch, Isabel, Alvarez, Miguel Angel, Seguí, José Ignacio, Mayordomo, Antonio, Antón, José Manuel, Baena, Arrate, Plazaola, Alfonso, Modolell, Amadeu, Pelegrí, Jose Ramón, Mel, Enrique, Aranda, Encarna, Adrover, José Valero, Alvarez, José Luis, García Puche, Pedro, Sánchez-Rovira, Sonia, Gonzalez, José Manuel, López-Vega, M Francisca, Garijo, GEICAM 9906 Study Investigators, [Martín,M] Department of Medical Oncology, Hospital Universitario San Carlos, Madrid, Spain. [López García-Asenjo,JA] Department of Pathology, Hospital Universitario San Carlos, Madrid, Spain. [Rodríguez-Lescure,A] Department of Medical Oncology, Hospital Universitario de Elche, Spain. [Ruiz,A] Department of Medical Oncology, Instituto Valenciano de Oncologia, Valencia, Spain. [Almenar,S] Department of Pathology, Instituto Valenciano de Oncologia, Valencia, Spain. [Alba Conejo,E] Department of Medical Oncology, Hospital Virgen de la Victoria, Málaga, Spain. [Calvo,L] Department of Medical Oncology, Complejo Hospitalario Juan Canalejo, La Coruña, Spain. [Guitián,MD] Department of Pathology, Complejo Hospitalario Juan Canalejo, La Coruña, Spain. [Ruiz-Borrego,M] Department of Medical Oncology, Hospital Vírgen del Rocío, Sevilla, Spain [Palacios,J] Department of Pathology, Hospital Vírgen del Rocío, Sevilla, Spain. [Muñárriz,B] Department of Medical Oncology, Hospital La Fe, Valencia, Spain. [Vera,F] Department of Pathology, Hospital La Fe, Valencia, Spain. [Rodríguez, CA] Department of Medical Oncology, Hospital Universitario de Salamanca, Salamanca, Spain. [Crespo,C] Department of Medical Oncology, Hospital Ramón y Cajal, Madrid, Spain. [González-Palacios,JF] Department of Pathology, Hospital Ramón y Cajal, Madrid, Spain. [de Álava,E] Department of Pathology, Centro de Investigación del Cáncer, Salamanca, Spain. [Ramos,M] Department of Medical Oncology, Centro Oncológico de Galicia, La Coruña, Spain. [Gracia Marco,JM] Department of Medical Oncology, Hospital de Cabueñes, Gijón, Spain. [Lluch,A] Department of Medical Oncology, Hospital Clínico Universitario de Valencia, Valencia, Spain. [Álvarez,I] Department of Medical Oncology, Hospital de Donostia, San Sebastián, Spain. [Seguí,MA] Department of Medical Oncology, Hospital Parc Taulí, Sabadell, Spain. [Mayordomo,JI] Department of Medical Oncology, Hospital Clínico Lozano Blesa, Zaragoza, Spain. [Antón,A] Department of Medical Oncology, Hospital Miguel Servet, Zaragoza, Spain. [Baena,JM] Department of Medical Oncology, Complejo Hospitalario Puerta del Mar, Cádiz, Spain. [Plazaola,A] Department of Medical Oncology, Instituto Oncológico de Guipúzcoa, San Sebastián, Spain. [Modolell,A] Department of Medical Oncology, Clínica Corachan, Barcelona, Spain. [Pelegrí,A] Department of Medical Oncology, Hospital Universitario San Joan de Reus, Tarragona, Spain. [Mel,JR] Department of Medical Oncology, Complejo Hospitalario Xeral Calde, Lugo, Spain. [Aranda,E] Department of Medical Oncology, Hospital Provincial de Córdoba, Córdoba, Spain. [Adrover,E] Department of Medical Oncology, Hospital General de Alicante, Alicante, Spain. [Valero Álvarez,J] Hospital Provincial de Zamora, Spain. [García Puche,JL] Department of Medical Oncology, Hospital San Cecilio de Granada, Granada, Spain. [Sánchez-Rovira,P] Department of Medical Oncology, Hospital Ciudad de Jaén, Jaén, Spain. [González,S] Department of Medical Oncology, Mutua de Terrasa, Terrasa, Spain. [López-Vega,JM] Department of Medical Oncology, Hospital Universitario Marqués de Valdecilla, Santander, Spain., and Department of Medical Oncology, Hospital Ciudad de Jaén, Jaén, Spain
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Oncology ,medicine.medical_treatment ,Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings] ,Supervivencia sin Enfermedad ,Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings] ,Chemicals and Drugs::Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases::Receptor Protein-Tyrosine Kinases::Receptor, erbB-2 [Medical Subject Headings] ,Antineoplastic Combined Chemotherapy Protocols ,Estimación de Kaplan-Meier ,Receptor erbB-2 ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Therapeutics::Clinical Protocols::Antineoplastic Protocols::Antineoplastic Combined Chemotherapy Protocols [Medical Subject Headings] ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Therapeutics::Drug Therapy::Drug Administration Schedule [Medical Subject Headings] ,Hazard ratio ,Pronóstico ,Epirrubicina ,Prognosis ,Immunohistochemistry ,Diseases::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Glandular and Epithelial::Carcinoma::Adenocarcinoma::Carcinoma, Ductal::Carcinoma, Ductal, Breast [Medical Subject Headings] ,Receptors, Estrogen ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Prognosis::Neoplasm Staging [Medical Subject Headings] ,Chemicals and Drugs::Biological Factors::Biological Markers::Tumor Markers, Biological [Medical Subject Headings] ,Receptors, Progesterone ,Chemicals and Drugs::Organic Chemicals::Hydrocarbons::Hydrocarbons, Cyclic::Hydrocarbons, Alicyclic::Cycloparaffins::Cyclodecanes::Taxoids::Paclitaxel [Medical Subject Headings] ,medicine.medical_specialty ,Paclitaxel ,Fluorouracilo ,Axillary lymph nodes ,Resultado del Tratamiento ,Anciano ,Disease-Free Survival ,Drug Administration Schedule ,Breast cancer ,Carcinoma Lobular ,Named Groups::Persons::Age Groups::Adult [Medical Subject Headings] ,Adjuvant therapy ,Humans ,Cyclophosphamide ,Aged ,ERBB2 protein, human ,medicine.disease ,Carcinoma, Lobular ,Check Tags::Female [Medical Subject Headings] ,Modelos de Riesgos Proporcionales ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Cytological Techniques::Histocytological Preparation Techniques::Staining and Labeling::In Situ Hybridization::In Situ Hybridization, Fluorescence [Medical Subject Headings] ,Health Care::Health Care Quality, Access, and Evaluation::Quality of Health Care::Health Care Evaluation Mechanisms::Statistics as Topic::Survival Analysis::Disease-Free Survival [Medical Subject Headings] ,Cancer Research ,Receptor, ErbB-2 ,Kaplan-Meier Estimate ,Antineoplásicos Fitogénicos ,Diseases::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Glandular and Epithelial::Carcinoma::Adenocarcinoma::Carcinoma, Lobular [Medical Subject Headings] ,Chemicals and Drugs::Heterocyclic Compounds::Heterocyclic Compounds, 1-Ring::Pyrimidines::Pyrimidinones::Uracil::Fluorouracil [Medical Subject Headings] ,Infusions, Intravenous ,In Situ Hybridization, Fluorescence ,Carcinoma, Ductal, Breast ,Neoplasias de la Mama ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Receptors, Cytoplasmic and Nuclear::Receptors, Steroid::Receptors, Estrogen [Medical Subject Headings] ,Middle Aged ,Chemotherapy regimen ,Treatment Outcome ,medicine.anatomical_structure ,Female ,Fluorouracil ,Breast disease ,Infusiones Intravenosas ,Chemicals and Drugs::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Antineoplastic Agents::Antineoplastic Agents, Phytogenic [Medical Subject Headings] ,Epirubicin ,medicine.drug ,Adult ,Protocolos de Quimioterapia Combinada Antineoplásica ,Hibridación Fluorescente In Situ ,Chemicals and Drugs::Organic Chemicals::Hydrocarbons::Hydrocarbons, Halogenated::Mustard Compounds::Nitrogen Mustard Compounds::Phosphoramide Mustards::Cyclophosphamide [Medical Subject Headings] ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::DNA-Binding Proteins::Receptors, Cytoplasmic and Nuclear::Receptors, Steroid::Receptors, Progesterone [Medical Subject Headings] ,Breast Neoplasms ,Ciclofosfamida ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Models, Theoretical::Models, Statistical::Proportional Hazards Models [Medical Subject Headings] ,Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biochemistry::Immunochemistry [Medical Subject Headings] ,Predictive Value of Tests ,Internal medicine ,Chemicals and Drugs::Organic Chemicals::Hydrocarbons::Hydrocarbons, Cyclic::Hydrocarbons, Aromatic::Polycyclic Hydrocarbons, Aromatic::Naphthacenes::Anthracyclines::Daunorubicin::Doxorubicin::Epirubicin [Medical Subject Headings] ,Biomarkers, Tumor ,medicine ,Named Groups::Persons::Age Groups::Adult::Aged [Medical Subject Headings] ,Diseases::Neoplasms::Neoplasms by Site::Breast Neoplasms [Medical Subject Headings] ,Neoplasm Staging ,Proportional Hazards Models ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Prognosis::Treatment Outcome [Medical Subject Headings] ,Receptores de Progesterona ,Chemotherapy ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Survival Analysis::Kaplan-Meier Estimate [Medical Subject Headings] ,business.industry ,Esquema de Medicación ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Therapeutics::Drug Therapy::Drug Administration Routes::Infusions, Parenteral::Infusions, Intravenous [Medical Subject Headings] ,Antineoplastic Agents, Phytogenic ,Estadificación de Neoplasias ,Receptores Estrogénicos ,Surgery ,Marcadores Biológicos de Tumor ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Prognosis [Medical Subject Headings] ,business ,Carcinoma Ductal de Mama ,Inmunohistoquímica - Abstract
Clinical Trial, Phase III; Comparative Study; Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't; BACKGROUND Taxanes are among the most active drugs for the treatment of metastatic breast cancer, and, as a consequence, they have also been studied in the adjuvant setting. METHODS After breast cancer surgery, women with lymph node-positive disease were randomly assigned to treatment with fluorouracil, epirubicin, and cyclophosphamide (FEC) or with FEC followed by weekly paclitaxel (FEC-P). The primary endpoint of study-5-year disease-free survival (DFS)-was assessed by Kaplan-Meier analysis. Secondary endpoints included overall survival and analysis of the prognostic and predictive value of clinical and molecular (hormone receptors by immunohistochemistry and HER2 by fluorescence in situ hybridization) markers. Associations and interactions were assessed with a multivariable Cox proportional hazards model for DFS for the following covariates: age, menopausal status, tumor size, lymph node status, type of chemotherapy, tumor size, positive lymph nodes, HER2 status, and hormone receptor status. All statistical tests were two-sided. RESULTS Among the 1246 eligible patients, estimated rates of DFS at 5 years were 78.5% in the FEC-P arm and 72.1% in the FEC arm (difference = 6.4%, 95% confidence interval [CI] = 1.6% to 11.2%; P = .006). FEC-P treatment was associated with a 23% reduction in the risk of relapse compared with FEC treatment (146 relapses in the 614 patients in the FEC-P arm vs 193 relapses in the 632 patients in the FEC arm, hazard ratio [HR] = 0.77, 95% CI = 0.62 to 0.95; P = .022) and a 22% reduction in the risk of death (73 and 95 deaths, respectively, HR = 0.78, 95% CI = 0.57 to 1.06; P = .110). Among the 928 patients for whom tumor samples were centrally analyzed, type of chemotherapy (FEC vs FEC-P) (P = .017), number of involved axillary lymph nodes (P < .001), tumor size (P = .020), hormone receptor status (P = .004), and HER2 status (P = .006) were all associated with DFS. We found no statistically significant interaction between HER2 status and paclitaxel treatment or between hormone receptor status and paclitaxel treatment. CONCLUSIONS Among patients with operable breast cancer, FEC-P treatment statistically significantly reduced the risk of relapse compared with FEC as adjuvant therapy. Yes
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- 2008
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39. Human pregnane X receptor is expressed in breast carcinomas, potential heterodimers formation between hPXR and RXR-alpha
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Isabel Conde, Julio Pérez, Benito Fraile, Ricardo Paniagua, Javier Zamora, Maria V.T. Lobo, Emilio Alba, Francisco González, María I. Arenas, Universidad de Alcalá. Departamento de Biología Celular y Genética, [Conde,I, Lobo,MVT, Pérez,J, Fraile,B, Paniagua,R, Arenas,MI] Department of Cell Biology and Genetics, University of Alcalá, Alcalá de Henares, Madrid, Spain. [Zamora,J] Clinical Biostatistics Unit, Hospital Ramón y Cajal, CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain. [González Sánchez,FJ, and Alba Conejo,E] Department of Medical Oncology, Hospital Universitario Virgen de la Victoria, Málaga, Spain. [Conde,I] Department of Cellular and Molecular Physiopathology, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.
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Ciencia ,SXR ,Pathology ,Receptors, Steroid ,Cancer Research ,Biología ,Named Groups::Persons::Age Groups::Adult::Aged::Aged, 80 and over [Medical Subject Headings] ,Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings] ,Supervivencia sin Enfermedad ,Receptores de Esteroides ,Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings] ,pregnane X receptor ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Clinical Laboratory Techniques::Cytological Techniques::Histocytochemistry::Immunohistochemistry [Medical Subject Headings] ,Breast cancer ,CIENCIA ,Aged, 80 and over ,Pregnane X receptor ,Adulto ,Neoplasia de la mama ,Carcinoma, Ductal, Breast ,Femenino ,Pregnane X Receptor ,SCIENCE ,Middle Aged ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Receptors, Cytoplasmic and Nuclear::Receptors, Steroid [Medical Subject Headings] ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Diseases::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Glandular and Epithelial::Carcinoma::Adenocarcinoma::Carcinoma, Ductal::Carcinoma, Ductal, Breast [Medical Subject Headings] ,Immunohistochemistry ,Humanos ,Heterodimers ,Human pregnane X receptor ,Oncology ,Phenomena and Processes::Chemical Phenomena::Biochemical Phenomena::Biochemical Processes::Dimerization [Medical Subject Headings] ,Female ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Prognosis::Neoplasm Staging [Medical Subject Headings] ,Dimerization ,Carcinoma in Situ ,Research Article ,Adult ,medicine.medical_specialty ,Western Blotting ,Science ,Anciano ,Receptores x Retinoide ,Blotting, Western ,Breast Neoplasms ,Retinoid X receptor ,Steroid biosynthesis ,Biology ,Carcinoma in situ ,lcsh:RC254-282 ,Disease-Free Survival ,medicine ,Named Groups::Persons::Age Groups::Adult [Medical Subject Headings] ,Genetics ,Dimerización ,Humans ,Named Groups::Persons::Age Groups::Adult::Aged [Medical Subject Headings] ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Prognosis::Disease-Free Survival [Medical Subject Headings] ,Diseases::Neoplasms::Neoplasms by Site::Breast Neoplasms [Medical Subject Headings] ,Aged ,Neoplasm Staging ,Receptor alfa X Retinoide ,Mediana edad ,Retinoid X Receptor alpha ,Retinoid X receptor alpha ,hPXR ,medicine.disease ,Diseases::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Glandular and Epithelial::Carcinoma::Carcinoma in Situ [Medical Subject Headings] ,Genética ,Estadificación de Neoplasias ,Anciano de 80 o más Años ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Receptors, Cytoplasmic and Nuclear::Receptors, Retinoic Acid::Retinoid X Receptors [Medical Subject Headings] ,Retinoid X Receptors ,Nuclear receptor ,Check Tags::Female [Medical Subject Headings] ,Cancer cell ,Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Chemistry Techniques, Analytical::Electrophoresis::Blotting, Western [Medical Subject Headings] ,Cancer research ,Carcinoma ductal de mama ,Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Receptors, Cytoplasmic and Nuclear::Receptors, Retinoic Acid::Retinoid X Receptors::Retinoid X Receptor alpha [Medical Subject Headings] ,Inmunohistoquímica - Abstract
14 p.-5 fig.-5 tab., [Background] The human pregnane X receptor (hPXR) is an orphan nuclear receptor that induces transcription of response elements present in steroid-inducible cytochrome P-450 gene promoters. This activation requires the participation of retinoid X receptors (RXRs), needed partners of hPXR to form heterodimers. We have investigated the expression of hPXR and RXRs in normal, premalignant, and malignant breast tissues, in order to determine whether their expression profile in localized infiltrative breast cancer is associated with an increased risk of recurrent disease., [Methods] Breast samples from 99 patients including benign breast diseases, in situ and infiltrative carcinomas were processed for immunohistochemistry and Western-blot analysis., [Results] Cancer cells from patients that developed recurrent disease showed a high cytoplasmic location of both hPXR isoforms. Only the infiltrative carcinomas that relapsed before 48 months showed nuclear location of hPXR isoform 2. This location was associated with the nuclear immunoexpression of RXR-alpha., [Conclusions] Breast cancer cells can express both variants 1 and 2 of hPXR. Infiltrative carcinomas that recurred showed a nuclear location of both hPXR and RXR-alpha; therefore, the overexpression and the subcellular location changes of hPXR could be considered as a potential new prognostic indicator.
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- 2008
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40. Oncogene-addicted solid tumors and microbiome-lung cancer as a main character: a narrative review.
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Guardamagna M, Meyer ML, Berciano-Guerrero MÁ, Mesas-Ruiz A, Cobo-Dols M, Perez-Ruiz E, Cantero Gonzalez A, Lavado-Valenzuela R, Barragán I, Oliver J, Garrido-Aranda A, Alvarez M, Rueda-Dominguez A, Queipo-Ortuño MI, Alba Conejo E, and Benitez JC
- Abstract
Background and Objective: Lung cancer stands as the main cause of cancer-related deaths worldwide. With the advent of immunotherapy and the discovery of targetable oncogenic driver genes, although prognosis has changed in the last few years, survival rates remain dismal for most patients. This emphasizes the urgent need for new strategies that could enhance treatment in precision medicine. The role of the microbiota in carcinogenesis constitutes an evolving landscape of which little is known. It has been suggested these microorganisms may influence in responses, resistance, and adverse effects to cancer treatments, particularly to immune checkpoint blockers. However, evidence on the impact of microbiota composition in oncogene-addicted tumors is lacking. This review aims to provide an overview of the relationship between microbiota, daily habits, the immune system, and oncogene-addicted tumors, focusing on lung cancer., Methods: A PubMed and Google Scholar search from 2013 to 2024 was conducted. Relevant articles were reviewed in order to guide our research and generate hypothesis of clinical applicability., Key Content and Findings: Microbiota is recognized to participate in immune reprogramming, fostering inflammatory, immunosuppressive, or anti-tumor responses. Therefore, identifying the microbiota that impact response to treatment and modulating its composition by interventions such as dietary modifications, probiotics or antibiotics, could potentially yield better outcomes for cancer patients. Additionally, targeted therapies that modulate molecular signaling pathways may impact both immunity and microbiota. Understanding this intricate interplay could unveil new therapeutic strategies., Conclusions: By comprehending how microbiota may influence efficacy of targeted therapies, even though current evidence is scarce, we may generate interesting hypotheses that could improve clinical practice., Competing Interests: Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://tlcr.amegroups.com/article/view/10.21037/tlcr-24-216/coif). The authors have no conflicts of interest to declare., (2024 Translational Lung Cancer Research. All rights reserved.)
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- 2024
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41. Role of poly-ADP-ribose polymerase inhibitors after brain progression in platinum-sensitive ovarian cancer: a case report and review of the literature.
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Lendinez-Sanchez G, Diaz-Redondo T, Iglesias-Campos M, Garrido-Almazán L, Alba-Conejo E, Rueda-Dominguez A, and Sanchez-Muñoz A
- Abstract
Introduction: The incidence of brain metastases in ovarian cancer is quite rare, being approximately 1%-2%. According to retrospective studies, patients with BRCA 1/2 mutations present a higher risk. The trimodal approach based on surgery, radiotherapy, and chemotherapy presents better outcomes, but the prognosis remains poor with overall survival since the brain progression is around 1 year. Poly-ADP-ribose polymerase inhibitors (PARPi) have provided a new alternative for the management of advanced ovarian cancer. The SOLO2, NOVA, and ARIEL3 clinical trials do not refer data on patients with brain metastases, and the published evidence for PARPi in this setting comes only from case reports and retrospective studies., Case Report: We present the case of a 54-year-old woman with stage IV ovarian high-grade serous papillary carcinoma who, after 37 months of treatment with olaparib, presented a single brain lesion. After radical treatment with surgery and adjuvant whole-brain radiotherapy, she resumed olaparib with no evidence of disease during 15 months. After a second single brain relapse treated with stereotactic radiosurgery, the patient continued olaparib beyond the brain progression with no evidence of extracranial disease. Despite that there were no changes in size or number of brain lesions, the neurological situation progressively worsened and the patient died 8 months after the second progression., Discussion: The higher incidence of brain metastases of ovarian cancer points out a possible tropism for the CNS in BRCA-mutated patients. In preclinical studies, PARPi has shown to cross the blood-brain barrier, with possible antitumor activity in the central nervous system (CNS) while maintaining control of extracranial disease. The best survival data are obtained with a trimodal approach, and adding a PARPi could improve the survival outcomes in the context of platinum-sensitivity disease. Targeted therapies combined with local treatments are also used in other malignancies, suggesting potential effectiveness due to tumor heterogeneity. PARPi before brain metastasis may delay its diagnosis, and using iPARP after brain metastases could improve the outcome of this population., Conclusion: The role that PARPi may have in the treatment of brain metastases of ovarian cancer requires more studies. In the context of radical treatment of brain metastasis (surgery and/or RT), with no evidence of extracranial disease, maintaining treatment with PARPi beyond the brain progression should be considered., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Lendinez-Sanchez, Diaz-Redondo, Iglesias-Campos, Garrido-Almazán, Alba-Conejo, Rueda-Dominguez and Sanchez-Muñoz.)
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- 2024
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42. Forearm Muscle Activity During the Handgrip Test in Breast Cancer Survivors: A Cross-Sectional Study.
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Fuentes-Abolafio IJ, Roldán-Jiménez C, Campos MI, Pajares-Hachero BI, Alba-Conejo E, and Cuesta-Vargas A
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- Humans, Adult, Middle Aged, Aged, Female, Forearm physiology, Hand Strength physiology, Cross-Sectional Studies, Neoplasm Recurrence, Local, Fatigue diagnosis, Fatigue etiology, Muscles, Breast Neoplasms, Cancer Survivors
- Abstract
Introduction/background: Breast cancer survivors (BCS) frequently show upper limb dysfunctions. The forearm muscle activity measured by surface electromyography (sEMG) in this population has not been studied. This study aimed to describe forearm muscle activity in BCS, as well as to assess its possible relationship with other variables related to upper limb functionality and cancer-related fatigue (CRF)., Materials and Methods: A cross-sectional study was carried out including 102 BCS as volunteers at a secondary care in Malaga, Spain. BCS were included if they were aged between 32 and 70 years old, without evidence of cancer recurrence at the time of recruitment. The forearm muscle activity (microvolts, µV) was assessed by sEMG during the handgrip test. The handgrip strength was assessed by dynamometry (kg), the upper limb functionality (%) was measured by the upper limb functional index (ULFI) questionnaire and the CRF was also assessed by revised Piper Fatigue Scale (0-10 points)., Results: BCS reported reduced forearm muscle activity (287.88 µV) and reduced handgrip strength (21.31 Kg), a good upper limb functionality (68.85%), and a moderate cancer-related fatigue (4.74). Forearm muscle activity showed a poor significant correlation (r = -0.223, P = .038) with the CRF. Handgrip strength showed a poor correlation with the upper limb functionality (r = 0.387, P < .001) and age (r=-0.200, P = .047)., Conclusion: BCS showed a reduced forearm muscle activity. BCS also presented a poor correlation between forearm muscle activity and handgrip strength. Both outcomes tended to lower values with higher levels of CRF, while preserving a good upper limb functionality., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2023
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43. Validation of the Upper Limb Functional Index on Breast Cancer Survivor.
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Martín-Martín J, Pajares-Hachero B, Alba-Conejo E, Ribelles N, Cuesta-Vargas AI, and Roldán-Jiménez C
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- Humans, Female, Surveys and Questionnaires, Reproducibility of Results, Disability Evaluation, Upper Extremity, Psychometrics, Breast Neoplasms, Cancer Survivors, Musculoskeletal Diseases diagnosis
- Abstract
Breast cancer survivors (BCS) may face functional alterations after surgical intervention. Upper Limb Disorders (ULDs) are highly prevalent even years after a diagnosis. Clinicians may assess the upper limbs after breast cancer. The Upper Limb Functional Index (ULFI) has been validated across different populations and languages. This study aimed to assess the psychometric properties of the Upper Limb Functional Index Spanish version (ULFI-Sp) in the BCS., Methods: A psychometric validation study of the ULFI-Sp was conducted on 216 voluntary breast cancer survivors. The psychometric properties were as follows: analysis of the factor structure by maximum likelihood extraction (MLE), internal consistency, and construct validity by confirmatory factor analysis (CFA)., Results: The factor structure was one-dimensional. ULFI-Sp showed a high internal consistency for the total score (α = 0.916) and the regression score obtained from MLE (α = 0.996). CFA revealed a poor fit, and a new 14-item model (short version) was further tested. The developed short version of the ULFI-SP is preferable to assess upper limb function in Spanish BCS., Conclusions: Given the high prevalence of ULD in this population and the broader versions of ULFI across different languages, this study's results may be transferred to clinical practice and integrated as part of upper limb assessment after breast cancer.
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- 2023
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44. PD-L1 immunoexpression and molecular characterization of histological subtypes in urothelial carcinoma.
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Dawid de Vera MT, Prieto Cuadra JD, Álvarez Pérez M, Garrido-Aranda A, Alba Conejo E, and Hierro Martín I
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- Humans, B7-H1 Antigen analysis, Carcinoma, Transitional Cell genetics, Carcinoma, Transitional Cell pathology, Urinary Bladder Neoplasms genetics, Urinary Bladder Neoplasms pathology
- Abstract
Introduction: Urothelial carcinoma (UC) has histological subtypes whose phenotype reflects their molecular diversity, behavior and response to conventional therapy. Immune checkpoint inhibitors (ICIs) have improved the management of UC by evaluation of PD-L1. In the case of PD-L1 22C3, the initiation of ICI is considered from a combined positive score (CPS) greater than 10. However, UC subtypes with absent PD-L1 22C3 expression in cases with CPS>10 may not respond to these treatments. This study aims to establish a correlation between the PD-L1 immunoexpression and molecular alterations in divergent differentiation and histological subtypes of UC (UC-s)., Material and Methods: Twenty-six samples of UC were detected from a total of 24 patients. Two pathologists performed separately an assessment of UC-s on hematoxylin-eosin as well as PD-L1 expression. Molecular study of each case was performed by next generation sequencing (NGS). A descriptive analysis of the variables included was conducted., Results: Nine cases (34.61%) showed a CPS>10, some with negative PD-L1 immunoexpression in aggressive UC-s. The molecular study revealed alterations in genes belonging to the p53/cell cycle control, RAS, and DNA repair pathways, among others. None of the alterations were exclusive to any histological subtype., Discussion: Special attention should be paid to CPS>10 cases that include histological subtypes of UC with divergent expression for PD-L1 as they may not respond to treatment with ICI. We recommend examining the proportion and PD-L1 status of each subtype, especially if it has aggressive behavior., (Copyright © 2022 Sociedad Española de Anatomía Patológica. Publicado por Elsevier España, S.L.U. All rights reserved.)
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- 2023
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45. The Benefits of a Therapeutic Exercise and Educational Intervention Program on Central Sensitization Symptoms and Pain-Related Fear Avoidance in Breast Cancer Survivors.
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Gutiérrez-Sánchez D, Pajares-Hachero BI, Trinidad-Fernández M, Escriche-Escuder A, Iglesias-Campos M, Bermejo-Pérez MJ, Alba-Conejo E, Roldán-Jiménez C, and Cuesta-Vargas A
- Subjects
- Central Nervous System Sensitization, Fear, Female, Humans, Pain, Breast Neoplasms complications, Breast Neoplasms therapy, Cancer Survivors
- Abstract
Background: Central sensitization symptoms and pain-related fear avoidance are two common problems in breast cancer survivors. Non-pharmacologic interventions such as therapeutic exercise and patient education can be effective in this population., Aims: This study aimed to: (1) analyze the benefits of a therapeutic exercise and educational program on central sensitization symptoms and pain-related fear avoidance in breast cancer survivors, and (2) explore the association between pain-related fear avoidance and central sensitization symptoms., Design: A single group pre-post intervention study was conducted., Methods: Patients were recruited from the service of Medical Oncology of the University Clinical Hospital Virgen de la Victoria, in Málaga (Spain). The intervention consisted of a therapeutic exercise and educational program that lasted 12 weeks, twice a week, for 1 hour. Two instruments were used: the Spanish version of the Central Sensitization Inventory and the Spanish Fear Avoidance Components Scale., Results: A total of 82 breast cancer survivors participated in the study. Pre-post change on Central Sensitization Inventory was statistically significant (p = .007). There was a trend towards a significant difference for the Spanish Fear Avoidance Components Scale (p = .062). There was a statistically significant correlation between pain-related fear avoidance and central sensitization symptoms (r = 0.536, p < .001)., Conclusions: The current study has provided preliminary evidence on the benefits of this intervention in pain-related fear avoidance and central sensitization symptoms in breast cancer survivors. The Spanish version of the Central Sensitization Inventory and the Spanish Fear Avoidance Components Scale demonstrated responsiveness to change., Competing Interests: Declarations of Competing Interest None., (Copyright © 2022 American Society for Pain Management Nursing. Published by Elsevier Inc. All rights reserved.)
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- 2022
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46. The economic cost of not coding disease-related malnutrition: A study in cancer inpatients.
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Ruiz-García I, Contreras-Bolívar V, Sánchez-Torralvo FJ, Ulloa-Díaz O, Ruiz-Vico M, Abuín-Fernández J, Barrios-García M, Alba-Conejo E, and Olveira G
- Subjects
- Cost-Benefit Analysis, Female, Humans, Inpatients statistics & numerical data, Male, Malnutrition etiology, Middle Aged, Neoplasms complications, Nutrition Assessment, Patient Discharge statistics & numerical data, Prevalence, Prospective Studies, Clinical Coding economics, Diagnosis-Related Groups economics, Insurance, Health, Reimbursement statistics & numerical data, Malnutrition economics, Neoplasms economics
- Abstract
Background & Aims: Disease-related malnutrition (DRM) coding rate is usually low in hospitalised patients. The objective of our study was to estimate the percentage of correct DRM coding in cancer inpatients and to calculate the economic losses caused by such lack of coding., Methods: This was an observational, prospective study that was conducted in patients hospitalised in the Medical Oncology Unit of our hospital. A nutritional assessment was performed through subjective global assessment (SGA). The all patient refined-diagnosis related group (APR-DRG) weights were obtained at the moment of discharge; moreover, recalculation was done after including the diagnosis of malnutrition in the medical record of those patients in whom it had not been initially coded. The associated cost reimbursement were calculated based on the weight before and after revising the diagnosis of DRM., Results: A total of 266 patients were evaluated. From them, 220 (82.7%) suffered from DRM according to the SGA. In 137 (51.5%) of these patients, diagnosis was coded, as opposed to 83 (31.2%) cases (33 subjects with moderate and 50 with severe DRM) in whom it was not coded. The sum of the APR-DRG weights before revising the diagnosis of malnutrition was 343.4 points (mean: 1.29 ± 0.89). Whereas, after revising the diagnosis, it increased up to 384.3 (1.44 ± 0.96). The total cost reimbursement for the hospital before revising the diagnosis of malnutrition was 1,607,861.21€ and after revision it increased up to 1,799,199.69€, which means that 191,338.48€ were not reimbursed to the hospital due to the lack of coding of malnutrition. The cost reimbursement for each admission increased an average of 719.32€., Conclusion: The prevalence of DRM in cancer inpatients is high. Nevertheless, the diagnosis is not coded in one third of patients, which results in important economic losses for the hospitals., Competing Interests: Conflict of interest This study was partially funded by an unrestricted grant from Abbott Laboratories SA (Spain). All authors declare independence from the sponsoring body in the design, execution, and analysis of results and the compiling of the conclusions, and deny any conflicts of interest., (Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.)
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- 2022
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47. Subclinical Arteriosclerosis is Associated With Common Vascular Risk Factors in Long-Term Survivors of Testicular Cancer.
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Espíldora-Hernández J, Díaz-Antonio T, Baena-Espinar J, Alonso-Calderón I, Rioja J, Alba-Conejo E, Valdivielso P, and Sánchez-Chaparro MÁ
- Abstract
Cardiovascular disease risk is increased in survivors of testicular cancer because of exposure to treatment (chemotherapy and radiotherapy), as well as modification in lifestyle. Our aim was to assess the presence of subclinical arteriosclerosis in survivors of testicular cancer in comparison with a control group. This was a cross-sectional, observational, case-control study including 50 survivors of Germ Cell Tumor (GCT) (14 years of follow-up) and 53 age-matched controls with no cancer. We registered clinical data, cardiovascular risk factors, physical and Mediterranean questionnaires, intima-media thickness and plaque at carotid and femoral arteries by ultrasound, calcium score at the abdominal aorta, and liver steatosis by computed tomography, and applied analytical tests to quantify metabolic risk factors and inflammation markers. Patients showed a trend toward greater intima-media thickness (IMT) and plaques than controls, as well as a higher calcium score in the abdominal aorta. Remarkably, patients had higher waist circumference, insulin resistance (HOMA-IR), and liver steatosis, but lower physical activity and high-density lipoprotein (HDL) cholesterol than controls (all p < 0.05). In multivariate analyses, only common vascular risk factors were associated with subclinical arteriosclerosis. As a conclusion, in our study, a higher rate of subclinical arteriosclerosis in testicular cancer survivors was associated with classical metabolic risk factors and lifestyle, but not with exposure to chemotherapy., Competing Interests: The authors declare no conflict of interest.
- Published
- 2020
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48. Procalcitonin and white blood cells, combined predictors of infection in cardiac surgery patients.
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Heredia-Rodríguez M, Bustamante-Munguira J, Lorenzo M, Gómez-Sánchez E, Álvarez FJ, Fierro I, Conejo E, and Tamayo E
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Biomarkers blood, Cardiopulmonary Bypass, Case-Control Studies, Female, Humans, Leukocyte Count, Logistic Models, Male, Middle Aged, Postoperative Complications blood, Prospective Studies, Sepsis blood, Sepsis etiology, Young Adult, C-Reactive Protein metabolism, Calcitonin blood, Cardiac Surgical Procedures, Postoperative Complications diagnosis, Sepsis diagnosis
- Abstract
Background: Sepsis is strongly associated with an increased risk of postoperative mortality, longer length of hospital stay, and elevated health care costs. Early clinical symptoms overlap with those of systemic inflammatory response syndrome, a response that commonly occurs after cardiac surgery with cardiopulmonary bypass. Since a combination of biomarkers has been demonstrated to improve the prediction of postoperative infection, the objective of the present study was to test whether the combination of C-reactive protein (CRP), white blood cells (WBC), and procalcitonin (PCT) is able to predict postoperative infection in a large cohort of cardiac surgery patients., Material and Methods: Case-control study involving 423 patients who underwent cardiac surgery with cardiopulmonary bypass. Patients were retrospectively classified into two groups based on whether they developed severe sepsis or septic shock during the postoperative period. Blood samples for biological measurements (PCT, CRP, and WBC) were drawn on the first day in the intensive care unit, then once daily in the morning until the 10th postoperative day., Results: CRP median values were similar in both groups. WBC and PCT median values were significantly higher in patients with infection than without during the first 10 postoperative days. With elevation cutoffs ≤3 times (OR: 4.058; 95% CI: 2.206-7.463; P = 0.001) and ≥4 times (OR: 10.274, 95% CI: 3.690-28.604; P < 0.001), the median value for PCT (1.7 ng/mL) and/or WBC (13,000 cells/mm
3 ) on the second postoperative day was significantly associated with the development of infection., Conclusions: The goal of this study was to use a large cohort of cardiac surgery patients to ensure that the results were representative of this population. The combination of PCT and WBC levels over the first three postoperative days was able to predict postoperative infection within the 30 d following cardiac surgery., (Copyright © 2017 Elsevier Inc. All rights reserved.)- Published
- 2017
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49. Neural network implementation for a reversal procedure for water and dry matter estimation on plant leaves using selected LED wavelengths.
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Conejo E, Frangi JP, and de Rosny G
- Abstract
An inversion method based on a neural network was used to estimate water and dry matter contents on plant leaves, from transmittance and reflectance measurements, using light emitting diodes (LEDs) at specific wavelengths in NIR and FIR. The preliminary results for the predicted water content by the neural network method showed a RMSE value of 0.0027 g/cm(2) and |σ| value of approximately 3.53%, computed on 127 plant leaf samples over 51 species. Dry matter estimation also was performed, which showed potential implementation after future improvements. We believe this inversion method could be implemented in a portable system based on any silicon platform with the capability to perform in situ measurements on plant tissue.
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- 2015
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50. The role of immunohistochemistry in breast cancer patients treated with neoadjuvant chemotherapy: an old tool with an enduring prognostic value.
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Sánchez-Muñoz A, Plata-Fernández YM, Fernández M, Jaén-Morago A, Fernández-Navarro M, de la Torre-Cabrera C, Ramirez-Tortosa C, Lomas-Garrido M, Llácer C, Navarro-Perez V, Alba-Conejo E, and Sánchez-Rovira P
- Subjects
- Adolescent, Adult, Aged, Breast Neoplasms metabolism, Breast Neoplasms mortality, Carcinoma, Ductal, Breast metabolism, Carcinoma, Ductal, Breast mortality, Carcinoma, Lobular metabolism, Carcinoma, Lobular mortality, Cyclophosphamide administration & dosage, Deoxycytidine administration & dosage, Deoxycytidine analogs & derivatives, Doxorubicin administration & dosage, Epirubicin administration & dosage, Female, Follow-Up Studies, Humans, Immunoenzyme Techniques, Ki-67 Antigen metabolism, Middle Aged, Neoplasm Staging, Paclitaxel administration & dosage, Prognosis, Prospective Studies, Receptor, ErbB-2 metabolism, Receptors, Progesterone metabolism, Remission Induction, Retrospective Studies, Survival Rate, Young Adult, Gemcitabine, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Biomarkers, Tumor metabolism, Breast Neoplasms drug therapy, Carcinoma, Ductal, Breast drug therapy, Carcinoma, Lobular drug therapy, Neoadjuvant Therapy, Receptors, Estrogen metabolism
- Abstract
Background: To assess the molecular subtypes determined by hormonal receptors (HR) and human epidermal growth factor receptor 2 (HER2) status and the role of proliferation measured by the Ki-67 marker as predictive and prognostic factors in breast cancer patients treated with neoadjuvant chemotherapy., Methods: A total of 127 breast cancer patients were treated with neoadjuvant chemotherapy every 2 weeks as part of 2 studies. Study A consisted of the administration of Adriamycin (40 mg/m(2)) on day 1 plus paclitaxel (150 mg/m(2)) and gemcitabine 2000 mg/m(2)) on day 2 for 6 cycles (n = 54). Study B consisted of the administration of epirubicin (90 mg/m(2)), cyclophosphamide (600 mg/m(2)) on day 1 for 3 cycles, followed by the administration of paclitaxel (150 mg/m(2)) and gemcitabine 2500 (mg/m(2)) on day 1 with or without trastuzumab according to HER2 status (n = 73). In study A, patients did not receive trastuzumab regardless of HER2 status. The molecular subtypes of the patients with breast cancer were classified as 49% HR(+)/HER2(-), 17.5% HR(+)/HER2(+), 13.5% HR(-)/HER2(+), and 20% HR(-)/HER2(-)., Results: Pathologic complete response (pCR), defined as the absence of invasive cells in the breast and the lymph nodes, was achieved in 35 (28%) patients. The pCR rate was significantly different between the molecular subtypes of breast cancer, with 9% in HR(+)/HER2(-), 23% in HR(+)/HER2(+), 50% in HR(-)/HER2(+), and 56% in HR(-)/HER2(-) tumors (P < .001). The pCR rate was significantly higher in tumors that had high Ki-67 (≥20%) expression and were HR(-). HER2(+) was associated with a higher trend of pCR but did not reach statistical significance. The median follow-up was 81 months (r = 15-150 months). Patients who achieved a pCR had a significantly lower recurrence (P = .01) and higher overall survival (P = .02) compared with those who did not achieve pCR. A multivariate analysis revealed that pCR (hazard ratio 0.24 [95% CI, 0.07-0.7]; P = .019), the molecular subtype (hazard ratio 0.3 [95% CI, 0.1-0.8]; P = .02), and the Ki-67 index (hazard ratio 3.2 [95% CI, 1.4-7.1]; P = .004) were significant independent predictors of disease-free survival. Similar results were obtained for overall survival, in which the pCR rate (hazard ratio 0.119 [95% CI, 0.028-0.5]; P = .004), the molecular subtype (hazard ratio 0.17 [95% CI, 0.03-0.86]; P = .02), and the Ki-67 index (hazard ratio 3.6 [95% CI, 1.3-9.7]; P = .01) also displayed a significant influence on survival., Conclusions: Molecular subtypes and Ki-67 index were independent prognostic factors for disease-free survival and overall survival in breast cancer patients treated with neoadjuvant chemotherapy. A high rate of Ki-67 and HR(-) expression were predictors of pCR., (Copyright © 2013 Elsevier Inc. All rights reserved.)
- Published
- 2013
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