50 results on '"Franzi F"'
Search Results
2. Indicators of guideline-concordant care in lung cancer defined with a modified Delphi method and piloted in a cohort of over 5,800 cases
- Author
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Andreano, A, Valsecchi, M, Russo, A, Siena, S, Andruccioli, M, Ardizzoia, A, Assi, A, Baisi, A, Bedini, A, Beretta, G, Bersani, M, Bertagna, F, Berti, E, Bertolini, A, Bettini, A, Bignardi, M, Bini, F, Bna, C, Bono, F, Ottoni, D, Borghesi, A, Borghetti, P, Brunelli, A, Buffoli, A, Cacioppo, C, Calati, A, Calcagno, A, Casagrande, S, Casartelli, C, Castellani, M, Castro, A, Catalano, G, Catena, L, Ceresoli, G, Cergnul, M, Ciocia, G, Colombo, A, Conti, B, Corti, D, Cortinovis, D, Cozzi, C, Crippa, F, De Monte, A, Candis, D, De Toma, D, De Marinis, F, Dimarco, B, Di Nuovo, F, Doglioni, C, Fabbris, V, Faccioli, P, Fagnani, D, Farina, G, Fariselli, L, Filipazzi, V, Franzi, F, Frata, P, Gajate, A, Gardani, G, Gasparini, M, Giordano, M, Grignani, F, Landoni, C, Lombardi, C, Lombardi, F, Luciani, A, Maffioli, L, Marchione, R, Mariani, P, Maspero, A, Meriggi, F, Miedico, A, Morbini, P, Muriana, G, Orlandoni, G, Paris, E, Pedrazzoli, P, Pepe, G, Pezzica, E, Piccoli, F, Pinotti, G, Quadri, A, Ravasio, A, Ravenna, F, Ricchiuti, E, Rinaldo, D, Roda, G, Rossi, G, Santoro, A, Soatti, C, Stiglich, F, Tagliabue, L, Tirelli, V, Tironi, A, Tomirotti, M, Travaini, L, Ucci, G, Vaghi, A, Vanzulli, A, Veronesi, G, Vittimberga, I, Zambelli, C, Andreano A., Valsecchi M. G., Russo A. G., Siena S., Andruccioli M., Ardizzoia A., Assi A., Baisi A., Bedini A. V., Beretta G., Bersani M., Bertagna F., Berti E., Bertolini A., Bettini A., Bignardi M., Bini F., Bna C., Bono F., Ottoni D. B., Borghesi A., Borghetti P., Brunelli A., Buffoli A., Cacioppo C., Calati A., Calcagno A., Casagrande S., Casartelli C., Castellani M., Castro A., Catalano G., Catena L., Ceresoli G. L., Cergnul M., Ciocia G., Colombo A., Conti B., Corti D., Cortinovis D., Cozzi C., Crippa F., De Monte A., Candis D. D., De Toma D., De Marinis F., DiMarco B., Di Nuovo F., Doglioni C., Fabbris V., Faccioli P., Fagnani D., Farina G., Fariselli L., Filipazzi V., Franzi F., Frata P., Gajate A. M. S., Gardani G., Gasparini M., Giordano M., Grignani F., Landoni C., Lombardi C., Lombardi F., Luciani A., Maffioli L. S., Marchione R., Mariani P., Maspero A., Meriggi F., Miedico A., Morbini P., Muriana G., Orlandoni G., Paris E., Pedrazzoli P., Pepe G., Pezzica E., Piccoli F., Pinotti G., Quadri A., Ravasio A., Ravenna F., Ricchiuti E., Rinaldo D., Roda G., Rossi G., Santoro A., Soatti C. P., Stiglich F., Tagliabue L., Tirelli V., Tironi A., Tomirotti M., Travaini L. L., Ucci G., Vaghi A., Vanzulli A., Veronesi G., Vittimberga I., Zambelli C., Andreano, A, Valsecchi, M, Russo, A, Siena, S, Andruccioli, M, Ardizzoia, A, Assi, A, Baisi, A, Bedini, A, Beretta, G, Bersani, M, Bertagna, F, Berti, E, Bertolini, A, Bettini, A, Bignardi, M, Bini, F, Bna, C, Bono, F, Ottoni, D, Borghesi, A, Borghetti, P, Brunelli, A, Buffoli, A, Cacioppo, C, Calati, A, Calcagno, A, Casagrande, S, Casartelli, C, Castellani, M, Castro, A, Catalano, G, Catena, L, Ceresoli, G, Cergnul, M, Ciocia, G, Colombo, A, Conti, B, Corti, D, Cortinovis, D, Cozzi, C, Crippa, F, De Monte, A, Candis, D, De Toma, D, De Marinis, F, Dimarco, B, Di Nuovo, F, Doglioni, C, Fabbris, V, Faccioli, P, Fagnani, D, Farina, G, Fariselli, L, Filipazzi, V, Franzi, F, Frata, P, Gajate, A, Gardani, G, Gasparini, M, Giordano, M, Grignani, F, Landoni, C, Lombardi, C, Lombardi, F, Luciani, A, Maffioli, L, Marchione, R, Mariani, P, Maspero, A, Meriggi, F, Miedico, A, Morbini, P, Muriana, G, Orlandoni, G, Paris, E, Pedrazzoli, P, Pepe, G, Pezzica, E, Piccoli, F, Pinotti, G, Quadri, A, Ravasio, A, Ravenna, F, Ricchiuti, E, Rinaldo, D, Roda, G, Rossi, G, Santoro, A, Soatti, C, Stiglich, F, Tagliabue, L, Tirelli, V, Tironi, A, Tomirotti, M, Travaini, L, Ucci, G, Vaghi, A, Vanzulli, A, Veronesi, G, Vittimberga, I, Zambelli, C, Andreano A., Valsecchi M. G., Russo A. G., Siena S., Andruccioli M., Ardizzoia A., Assi A., Baisi A., Bedini A. V., Beretta G., Bersani M., Bertagna F., Berti E., Bertolini A., Bettini A., Bignardi M., Bini F., Bna C., Bono F., Ottoni D. B., Borghesi A., Borghetti P., Brunelli A., Buffoli A., Cacioppo C., Calati A., Calcagno A., Casagrande S., Casartelli C., Castellani M., Castro A., Catalano G., Catena L., Ceresoli G. L., Cergnul M., Ciocia G., Colombo A., Conti B., Corti D., Cortinovis D., Cozzi C., Crippa F., De Monte A., Candis D. D., De Toma D., De Marinis F., DiMarco B., Di Nuovo F., Doglioni C., Fabbris V., Faccioli P., Fagnani D., Farina G., Fariselli L., Filipazzi V., Franzi F., Frata P., Gajate A. M. S., Gardani G., Gasparini M., Giordano M., Grignani F., Landoni C., Lombardi C., Lombardi F., Luciani A., Maffioli L. S., Marchione R., Mariani P., Maspero A., Meriggi F., Miedico A., Morbini P., Muriana G., Orlandoni G., Paris E., Pedrazzoli P., Pepe G., Pezzica E., Piccoli F., Pinotti G., Quadri A., Ravasio A., Ravenna F., Ricchiuti E., Rinaldo D., Roda G., Rossi G., Santoro A., Soatti C. P., Stiglich F., Tagliabue L., Tirelli V., Tironi A., Tomirotti M., Travaini L. L., Ucci G., Vaghi A., Vanzulli A., Veronesi G., Vittimberga I., and Zambelli C.
- Abstract
Background: To identify indicators of guideline-concordant care in lung cancer, to implement such indicators with cancer registry data linked to health databases, and to pilot them in a cohort of patients from the cancer registry of the Milan Province. Methods: Thirty-four indicators were selected by revision of main guidelines by cancer epidemiologists, and then evaluated by a multidisciplinary panel of clinicians involved in lung cancer care and working on the pathway of lung cancer diagnosis and treatment in the Lombardy region, Italy. With a modified Delphi method, they assessed for each indicator the content validity as a quality measure of the care pathway, the degree of modifiability from the health professional, and the relevance to the health professional. Feasibility was assessed using the cancer registry and the routine health records of the Lombardy region. Feasible indicators were then calculated in the cohort of lung cancer patients diagnosed in 2007–2012 derived from the cancer registry of the Milan Province. Criterion validity was assessed reviewing clinical records of a random sample of 114 patients (threshold for acceptable discordance ≤20%). Finally, reliability was evaluated at the provider level. Results: Initially, 34 indicators were proposed for evaluation in the first Delphi round. Of the finally 22 selected indicators, 3 were not feasible because the required information was actually not available. The remaining 19 were calculated on the pilot cohort. After assessment of criterion validity (3 eliminated), 16 indicators were retained in the final set and evaluated for reliability. Conclusion: The developed and piloted set of indicators is now available to implement and monitor, over time, quality initiatives for lung cancer care in the studied health system.
- Published
- 2021
3. Impact of High-Grade Patterns in Early-Stage Lung Adenocarcinoma: A Multicentric Analysis
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Bertoglio, P., Aprile, V., Ventura, L., Cattoni, M., Nachira, D., Lococo, Filippo, Perez, M. R., Guerrera, F., Minervini, F., Querzoli, G., Bocchialini, G., Bacchin, D., Franzi, F., Rindi, Guido, Bellafiore, S., Femia, F., Bogina, G. S., Solli, P., Kestenholz, P., Ruffini, E., Paci, M., Margaritora, Stefano, Imperatori, A. S., Lucchi, M., Gnetti, L., Terzi, A. C., Lococo F. (ORCID:0000-0002-9383-5554), Rindi G. (ORCID:0000-0003-2996-4404), Margaritora S. (ORCID:0000-0002-9796-760X), Bertoglio, P., Aprile, V., Ventura, L., Cattoni, M., Nachira, D., Lococo, Filippo, Perez, M. R., Guerrera, F., Minervini, F., Querzoli, G., Bocchialini, G., Bacchin, D., Franzi, F., Rindi, Guido, Bellafiore, S., Femia, F., Bogina, G. S., Solli, P., Kestenholz, P., Ruffini, E., Paci, M., Margaritora, Stefano, Imperatori, A. S., Lucchi, M., Gnetti, L., Terzi, A. C., Lococo F. (ORCID:0000-0002-9383-5554), Rindi G. (ORCID:0000-0003-2996-4404), and Margaritora S. (ORCID:0000-0002-9796-760X)
- Abstract
Objective: The presence of micropapillary and solid adenocarcinoma patterns leads to a worse survival and a significantly higher tendency to recur. This study aims to assess the impact of pT descriptor combined with the presence of high-grade components on long-term outcomes in early-stage lung adenocarcinomas. Methods: We retrospectively collected data of consecutive resected pT1-T3N0 lung adenocarcinoma from nine European Thoracic Centers. All patients who underwent a radical resection with lymph-node dissection between 2014 and 2017 were included. Differences in Overall Survival (OS) and Disease-Free Survival (DFS) and possible prognostic factors associated with outcomes were evaluated also after performing a propensity score matching to compare tumors containing non-high-grade and high-grade patterns. Results: Among 607 patients, the majority were male and received a lobectomy. At least one high-grade histological pattern was seen in 230 cases (37.9%), of which 169 solid and 75 micropapillary. T1a-b-c without high-grade pattern had a significant better prognosis compared to T1a-b-c with high-grade pattern (p = 0.020), but the latter had similar OS compared to T2a (p = 0.277). Concurrently, T1a-b-c without micropapillary or solid patterns had a significantly better DFS compared to those with high-grade patterns (p = 0.034), and it was similar to T2a (p = 0.839). Multivariable analysis confirms the role of T descriptor according to high-grade pattern both for OS (p = 0.024; HR 1.285 95% CI 1.033–1.599) and DFS (p = 0.003; HR 1.196, 95% CI 1.054–1.344, respectively). These results were confirmed after the propensity score matching analysis. Conclusions: pT1 lung adenocarcinomas with a high-grade component have similar prognosis of pT2a tumors.
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- 2022
4. A0153 - Clinical characteristics and oncologic outcomes of bladder neuroendocrine carcinoma in a contemporary, multi-institutional cohort
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Zaffuto, E., Leni, R., Pini, G.M., Nicolini, L., Gianazza, S., Maragliano, R., Franzi, F., Famoso, G., Capogrosso, P., Gianesini, G., Carcano, G., Briganti, A., Montorsi, F., Colecchia, M., Uccella, S., and Dehò, F.
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- 2024
- Full Text
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5. OA06.02 High-Grade Patterns Cause the Upstaging of Lung Adenocarcinomas From T1 to T2a: A Multicentric Analysis
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Bertoglio, P., primary, Aprile, V., additional, Ventura, L., additional, Cattoni, M., additional, Nachira, D., additional, Lococo, F., additional, Rodriguez-Perez, M., additional, Guerrera, F., additional, Minervini, F., additional, Querzoli, G., additional, Bocchialini, G., additional, Bacchin, D., additional, Franzi, F., additional, Rindi, G., additional, Bellafiore, S., additional, Femia, F., additional, Bogina, G., additional, Solli, P., additional, Kestenholz, P., additional, Ruffini, E., additional, Paci, M., additional, Margaritora, S., additional, Imperatori, A., additional, Lucchi, M., additional, Gnetti, L., additional, and Terzi, A., additional
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- 2021
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6. Prognostic impact of lung adenocarcinoma second predominant pattern from a large European database
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Bertoglio, P., Querzoli, G., Ventura, L., Aprile, V., Cattoni, M. A., Nachira, Dania, Lococo, Filippo, Rodriguez Perez, M., Guerrera, F., Minervini, F., Gnetti, L., Bacchin, D., Franzi, F., Rindi, Guido, Bellafiore, S., Femia, F., Viti, A., Bogina, G. S., Kestenholz, P., Ruffini, E., Paci, M., Margaritora, Stefano, Imperatori, A. S., Lucchi, M., Ampollini, L., Terzi, A. C., Nachira D. (ORCID:0000-0003-2937-9678), Lococo F. (ORCID:0000-0002-9383-5554), Rindi G. (ORCID:0000-0003-2996-4404), Margaritora S. (ORCID:0000-0002-9796-760X), Bertoglio, P., Querzoli, G., Ventura, L., Aprile, V., Cattoni, M. A., Nachira, Dania, Lococo, Filippo, Rodriguez Perez, M., Guerrera, F., Minervini, F., Gnetti, L., Bacchin, D., Franzi, F., Rindi, Guido, Bellafiore, S., Femia, F., Viti, A., Bogina, G. S., Kestenholz, P., Ruffini, E., Paci, M., Margaritora, Stefano, Imperatori, A. S., Lucchi, M., Ampollini, L., Terzi, A. C., Nachira D. (ORCID:0000-0003-2937-9678), Lococo F. (ORCID:0000-0002-9383-5554), Rindi G. (ORCID:0000-0003-2996-4404), and Margaritora S. (ORCID:0000-0002-9796-760X)
- Abstract
Background and Objectives: Adenocarcinoma patterns could be grouped based on clinical behaviors: low- (lepidic), intermediate- (papillary or acinar), and high-grade (micropapillary and solid). We analyzed the impact of the second predominant pattern (SPP) on disease-free survival (DFS). Methods: We retrospectively collected data of surgically resected stage I and II adenocarcinoma. Selection criteria: anatomical resection with lymphadenectomy and pathological N0. Pure adenocarcinomas and mucinous subtypes were excluded. Recurrence rate and factors affecting DFS were analyzed according to the SPP focusing on intermediate-grade predominant pattern adenocarcinomas. Results: Among 270 patients, 55% were male. The mean age was 68.3 years. SPP pattern appeared as follows: lepidic 43.0%, papillary 23.0%, solid 14.4%, acinar 11.9%, and micropapillary 7.8%. The recurrence rate was 21.5% and 5-year DFS was 71.1%. No difference in DFS was found according to SPP (p =.522). In patients with high-grade SPP, the percentage of SPP, age, and tumor size significantly influenced DFS (p =.016). In patients with lepidic SPP, size, male gender, and lymph-node sampling (p =.005; p =.014; p =.038, respectively) significantly influenced DFS. Conclusions: The impact of SPP on DFS is not homogeneous in a subset of patients with the intermediate-grade predominant patterns. The influence of high-grade SPP on DFS is related to its proportion in the tumor.
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- 2021
7. P08.01 Prognostic Impact of Second Predominant Pattern in Lung Adenocarcinoma: Analysis From a Large Multicentric European Database
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Bertoglio, P., primary, Ventura, L., additional, Aprile, V., additional, Cattoni, M., additional, Nachira, D., additional, Lococo, F., additional, Rodriguez, M., additional, Guerrera, F., additional, Minervini, F., additional, Gnetti, L., additional, Bacchin, D., additional, Franzi, F., additional, Querzoli, G., additional, Rindi, G., additional, Bellafiore, S., additional, Femia, F., additional, Viti, A., additional, Kestenholz, P., additional, Ruffini, E., additional, Paci, M., additional, Margaritora, S., additional, Imperatori, A., additional, Lucchi, M., additional, Ampollini, L., additional, and Terzi, A., additional
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- 2021
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8. Gastric Xanthomatous Hyperplastic Polyps – Just an Incidental Endoscopic Finding?
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Piantanida, E., primary, Gallo, Daniela, additional, Dozio, E., additional, Trotti, E., additional, Piantanida, E., additional, Frattini, F., additional, Franzi, F., additional, Sessa, F., additional, Dionigi, G. L., additional, Sabatino, Jessica, additional, Bartalena, L., additional, Tanda, Maria Laura, additional, and Ippolito, Silvia, additional
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- 2020
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9. P2.17-29 Impact of Second Predominant Pattern on Recurrence in Early Stage Resected Lung Adenocarcinoma: A Multicentric Study
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Bertoglio, P., primary, Cattoni, M., additional, Nachira, D., additional, Lococo, F., additional, Aprile, V., additional, Rodriguez, M., additional, Guerrera, F., additional, Franzi, F., additional, Viti, A., additional, Bellafiore, S., additional, Rindi, G., additional, Bacchin, D., additional, Lozano Escario, M.D., additional, Femia, F., additional, Querzoli, G., additional, Tobar, L. Garcia, additional, Ruffini, E., additional, Paci, M., additional, Margaritora, S., additional, Lucchi, M., additional, Imperatori, A., additional, and Terzi, A., additional
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- 2019
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10. EGFR T790M detection in TKI-naïve NSCLCs carrying sensitive EGFR mutations
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Pinotti, G., primary, Cerutti, R., additional, Sahnane, N., additional, Lettig, L., additional, Albeni, C., additional, Tuzi, A., additional, Franzi, F., additional, Pastore, A., additional, Ogliari, F., additional, Sessa, F., additional, and Furlan, D., additional
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- 2017
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11. Detection of early genetic and epigenetic alterations in NSCLC by using mass spectrometry and pyrosequencing analysis
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Furlan, D., primary, Sahnane, N., additional, Rotolo, N., additional, Franzi, F., additional, Nardecchia, E., additional, Sessa, F., additional, Dominioni, L., additional, and Imperatori, A., additional
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- 2016
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12. Mixed exocrine-neuroendocrine carcinoma of the nasal cavity: clinico-pathologic and molecular study of a case and review of the literature
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La Rosa, S., Furlan, Daniela, Franzi, F., Battaglia, Paolo, Frattini, M., Zanellato, E., Marando, A., Sahnane, Nora, Turri Zanoni, M., Castelnuovo, PAOLO GIOCONDO MARIA, Capella, C., and LA ROSA, Stefano
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Male ,Molecular profile ,Pathology ,medicine.medical_specialty ,DNA Mutational Analysis ,Nose Neoplasms ,Case Report ,Adenocarcinoma ,Biology ,medicine.disease_cause ,Neuroendocrine differentiation ,Pathology and Forensic Medicine ,Mixed adenoneuroendocrine carcinoma ,Biomarkers, Tumor ,medicine ,Carcinoma ,Humans ,CDX2 ,Intestinal-type adenocarcinomas Neuroendocrine carcinoma Nasal cavity Mixed adenoneuroendocrine carcinoma Molecular profile ,Aged ,Intestinal-type adenocarcinomas ,Chromogranin A ,medicine.disease ,Immunohistochemistry ,Neoplasms, Complex and Mixed ,Carcinoma, Neuroendocrine ,Oncology ,Otorhinolaryngology ,Nasal cavity ,Neuroendocrine carcinoma ,Cancer research ,biology.protein ,Synaptophysin ,KRAS ,CDKN1B - Abstract
Sinonasal intestinal-type adenocarcinomas (ITACs) are rare neoplasms histologically resembling intestinal adenocarcinomas. Although a neuroendocrine differentiation in ITACs has been described, true mixed exocrine-neuroendocrine carcinomas, neoplasms in which each component represents at least 30 % of the lesion, are extremely rare and their molecular alterations are largely unknown. We describe herein the clinico-pathologic features, the methylation profile, chromosomal gains and losses, and mutation analysis of KRAS, BRAF and p53 in a nasal mixed exocrine-neuroendocrine carcinoma resected in a 79-year-old man. The tumor was composed of an ITAC and a poorly differentiated neuroendocrine carcinoma. Both exocrine and neuroendocrine components were CK8, CK20, CDX2 and p53 positive, and CK7 and TTF1 negative. The neuroendocrine component also showed immunoreactivity for chromogranin A, synaptophysin, serotonin and glicentin. Gains and losses were found at following chromosome regions: 17p13 (TP53), 14q24 (MLH3), 19q13 (KLK3), 5q21 (APC), 7q21 (CDK6), 9q34 (DAPK1), 12p13 (TNFRSF 1A, CDKN1B), 13q12 (BRCA2), 17p13.3 (HIC1), 18q21 (BCL2), and 22q12 (TIMP3). Aberrant methylation was detected only in the neuroendocrine component and involved APC and DAPK1 genes. No mutation of KRAS (exons 2–4), BRAF (exon 15), and p53 (exons 4–10) was found in both components. The results suggest a monoclonal origin of the tumor from a pluripotent cell undergoing a biphenotypic differentiation and that the neuroendocrine differentiation may be from an exocrine to an endocrine pathway. We have also reviewed the literature on sinonasal mixed exocrine-neuroendocrine carcinomas to give to the reader a comprehensive overview of these very rare tumor types.
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- 2013
13. Clinico-pathologic and prognostic study of 59 acinar cell carcinomas of the pancreas
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La Rosa, S., Adsay, V. N., Albarello, L., Asioli, S., Casnedi, S., Franzi, F., Marando, A., Notohara, K., Sessa, F., Alessandro Vanoli, Zhang, L., Capella, C., S La Rosa, VN Adsay, L Albarello, S Asioli, S Casnedi, F Franzi, A Marando, K Notohara, F Sessa, A Vanoli, L Zhang, and C Capella.
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PANCREAS - Abstract
Background: Due to its relative rarity, many clinicopathologic characteristics of acinar cell carcinoma (ACC) remain to be further elucidated and there are not established prognostic factors. Design: 59 ACCs were investigated for the following parameters: site, size, local infi ltration, node and distant metastases, architectural pattern (acinar, pseudoglandular, trabecular, solid structure), nuclear atypia, presence of necrosis, expanding versus infi ltrating growth, lymphovascular and perineural invasion, mitotic and Ki67 indices, BCL10, trypsin, CEL, amylase, lipase, PDX1, chromogranin A, CK19, CK7, and β-catenin expression. Results: The patients were predominantly males (M/F:2.3). Mean age was 59 years (28-88 years). Mean tumor size was 7.8 cm (2-29 cm). 32 tumors showed an acinar/ pseudoglandular pattern, while 27 a solid architecture often associated with an acinar/ trabecular structure. BCL10 and trypsin were the most reliable immunohistochemical markers, while amylase and lipase were not. 45 patients underwent surgery, while 14 showed unresectable cancers. Surgery was statistically correlated with a better prognosis (p:0.0007). 10 cases showing more than 25% chromogranin A positive cells were classifi ed as mixed endocrine/ACCs, but there was not a different survival between pure ACCs and mixed cancers. 12 patients were alive free of disease after a mean follow-up time of 78 months, 4 were alive with disease after a mean follow-up time of 43 months, while 34 died of disease after a mean follow-up time of 24 months. In operated patients, the factors signifi cantly correlated with poor prognosis were UICC-stage (p:0.003) and, in particular, size >6.5cm (p:0.04), lymph node (p:0.03) and distant (p:0.008) metastases. Vascular and perineural invasion and CK19 expression also showed a trend for poor prognosis, but did not reach statistical signifi cance. Conclusions: ACCs show heterogeneous morphological features. Factors associated with adverse prognosis are stage including resectability, size, lymph node and distant metastases.
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- 2012
14. Phenotypic and functional characterization of tumor infiltrating natural killer cells: role in tumor angiogenesis
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Bruno, A., Focaccetti, C., Pagani, A., Imperatori, ANDREA SELENITO, Spagnoletti, M., Ferlazzo, G., Mortara, Lorenzo, Franzi, F., Capella, CARLO RENATO, Albini, A., Dominioni, Lorenzo, and Noonan, Douglas
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- 2011
15. Localizzazione immunoistochimica ed ultrastrutturale dell’enzima BACE2 nel pancreas
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Placidi, C, Finzi, G, Franzi, F, Acquati, F, Palumbo, E, Russo, A, Taramelli, R, Sessa, F, and La Rosa, S
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- 2009
16. BCL10 Is a New Sensitive and Specific Marker of Pancreatic Acinar Cell Carcinoma
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La Rosa, S., Franzi, F., SILVIA MARCHET, Finzi, G., Chiaravalli, A. M., Vigetti, D., Sessa, F., and Capella, C.
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- 2009
17. 1335P - EGFR T790M detection in TKI-naïve NSCLCs carrying sensitive EGFR mutations
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Pinotti, G., Cerutti, R., Sahnane, N., Lettig, L., Albeni, C., Tuzi, A., Franzi, F., Pastore, A., Ogliari, F., Sessa, F., and Furlan, D.
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- 2017
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18. Ultrastructural evidence of Tropheryma whippelii in PAS-negative granulomatous lymph nodes
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Finzi, G, Franzi, F, Sessa, Fausto, Mastaglio, C, and Capella, CARLO RENATO
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- 2007
19. Clinico - Pathological profile of Estrogen and Progesteron receptors negatibe breast cancinomas with basal or luminal markers expression
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Dainese, E, Micello, D, Franzi, F, Riva, Cristina, Capella, C, and Sessa, Fausto
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- 2006
20. CLINICO-PATHOLOGICAL PROFILE OF ESTROGEN AND PROGESTERONE NEGATIVE BREAST CARCINOMAS WITH BASAL OR LUMINAL MARKERS EXPRESSION
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Dainese, L., Micello, D., Franzi, F., Riva, Cristina, Capella, C., and Sessa, F.
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- 2006
21. 120P - Detection of early genetic and epigenetic alterations in NSCLC by using mass spectrometry and pyrosequencing analysis
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Furlan, D., Sahnane, N., Rotolo, N., Franzi, F., Nardecchia, E., Sessa, F., Dominioni, L., and Imperatori, A.
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- 2016
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22. EGFR T790M detection rate in lung adenocarcinomas at baseline using droplet digital PCR and validation by ultra-deep next generation sequencing
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Monica Giordano, Fausto Sessa, Giancarlo Troncone, Roberta Cerutti, Alessandro Tuzi, Alessia Pastore, Antonella Bovio, Daniela Furlan, Graziella Pinotti, Francesca Rita Ogliari, Umberto Malapelle, Giovanni Veronesi, Nora Sahnane, Claudio Verusio, Chiara Albeni, Francesco Pepe, Lucio Lettig, Francesca Franzi, Lettig, L., Sahnane, N., Pepe, F., Cerutti, R., Albeni, C., Franzi, F., Veronesi, G., Ogliari, F., Pastore, A., Tuzi, A., Pinotti, G., Bovio, A., Verusio, C., Giordano, M., Troncone, G., Sessa, F., Malapelle, U., and Furlan, D.
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0301 basic medicine ,Oncology ,medicine.medical_specialty ,EGFR T790M ,EGFR T790M mutation ,MALDI-TOF mass spectrometry ,droplet digital PCR (ddPCR) ,real time quantitative PCR (AS-PCR) ,ultra-deep next generation sequencing (NGS) ,DNA sequencing ,03 medical and health sciences ,T790M ,0302 clinical medicine ,Internal medicine ,medicine ,Digital polymerase chain reaction ,Progression-free survival ,Lung cancer ,Lung ,business.industry ,medicine.disease ,respiratory tract diseases ,030104 developmental biology ,medicine.anatomical_structure ,Real-time polymerase chain reaction ,030220 oncology & carcinogenesis ,business - Abstract
Background Routine testing of baseline EGFR T790M mutation may have important clinical impact but many discordant data have been reported regarding the diagnostic, prognostic and predictive role of this marker. In this study we aimed to assess T790M frequency in 164 untreated EGFR-mutated NSCLCs using methods with different sensitivity as well as to analyze the relationship between baseline T790M mutation status, patient's clinicopathologic features and tyrosine kinase inhibitors (TKI) treatment outcomes. Methods We compared the diagnostic performance, sensitivity and specificity of three methods, namely MALDI-TOF mass spectrometry (MS), Allele-Specific Real Time PCR (AS-PCR), droplet digital PCR (ddPCR). Ultra-deep next generation sequencing (NGS) validation of T790M-mutant NSCLCs was performed using SiRe® panel. Results Baseline T790M occurred in 17% of the tumors. Intermediately sensitive techniques such as MALDI-TOF MS (detection limit of T790M ≥5%) allow to detect T790M in 2% of cases exhibiting mutant-allele fractions ranging from 11.5% to 17%. Median overall survival (OS) in these patients was poor (7.3 months) and progression free survival (PFS) was of 3.3 months in patients treated with a 1st generation EGFR TKI. The remaining T790M-positive cases showed very low mutant-allele fractions ranging from 0.07% to 0.38% and required highly sensitive methods such as ddPCR and NGS to be identified. All these cases showed a concurrent sensitizing EGFR mutation (mainly exon 19 deletion), and clinicopathological features similar to those observed in EGFR mutant cancers. Median OS of these patients was 27 months while median PFS after TKI treatment was 20 months. Conclusions Routine test of baseline EGFR T790M may have an important role in the prediction to EGFR TKI therapy response and should be performed using highly sensitive and quantitative methods, such as ddPCR and NGS, in order to reliably distinguish NSCLCs with high or very low T790M mutant-allele fraction.
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- 2019
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23. The proangiogenic phenotype of natural killer cells in patients with non-small cell lung cancer
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Adriana Albini, Antonino Bruno, Chiara Focaccetti, Andrea Imperatori, Arianna Pagani, Guido Ferlazzo, Lorenzo Mortara, Carlo Capella, Nicola Rotolo, Marco Spagnoletti, Douglas M. Noonan, Anna Rita Cantelmo, Francesca Franzi, Bruno, A, Focaccetti, C, Pagani, A, Imperatori, A, Spagnoletti, M, Rotolo, N, Cantelmo, A, Franzi, F, Capella, C, Ferlazzo, G, Mortara, L, Albini, A, and Noonan, D
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squamous cell carcinoma ,Male ,Cancer Research ,Lung Neoplasms ,medicine.medical_treatment ,Endothelial cell chemotaxis ,Biology ,Settore MED/04 ,non-small cell lung cancer ,natural killer cells ,tumor angiogenesis ,cytokines ,lcsh:RC254-282 ,Transforming Growth Factor beta1 ,Interleukin 21 ,chemistry.chemical_compound ,Carcinoma, Non-Small-Cell Lung ,Tumor Microenvironment ,medicine ,Humans ,Aged ,Neoplasm Staging ,Female ,Immunity, Innate ,Killer Cells, Natural ,Middle Aged ,Neovascularization, Pathologic ,Tumor microenvironment ,Lymphokine-activated killer cell ,Innate lymphoid cell ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Lung Neoplasm ,Vascular endothelial growth factor ,Cytokine ,chemistry ,Immunology ,Interleukin 12 ,Research Article ,Human - Abstract
The tumor microenvironment can polarize innate immune cells to a proangiogenic phenotype. Decidual natural killer (dNK) cells show an angiogenic phenotype, yet the role for NK innate lymphoid cells in tumor angiogenesis remains to be defined. We investigated NK cells from patients with surgically resected non-small cell lung cancer (NSCLC) and controls using flow cytometric and functional analyses. The CD56(+)CD16(-) NK subset in NSCLC patients, which represents the predominant NK subset in tumors and a minor subset in adjacent lung and peripheral blood, was associated with vascular endothelial growth factor (VEGF), placental growth factor (PIGF), and interleukin-8 (IL-8)/CXCL8 production. Peripheral blood CD56(+)CD16(-) NK cells from patients with the squamous cell carcinoma (SCC) subtype showed higher VEGF and PlGF production compared to those from patients with adenocarcinoma (AdC) and controls. Higher IL-8 production was found for both SCC and AdC compared to controls. Supernatants derived from NSCLC CD56(+)CD16(-) NK cells induced endothelial cell chemotaxis and formation of capillary-like structures in vitro, particularly evident in SCC patients and absent from controls. Finally, exposure to transforming growth factor-β(1) (TGFβ(1)), a cytokine associated with dNK polarization, upregulated VEGF and PlGF in peripheral blood CD56(+)CD16(-) NK cells from healthy subjects. Our data suggest that NK cells in NSCLC act as proangiogenic cells, particularly evident for SCC and in part mediated by TGFβ(1).
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- 2013
24. Clinicopathologic Study of 62 Acinar Cell Carcinomas of the Pancreas: Insights Into the Morphology and Immunophenotype and Search for Prognostic Markers
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Kenji Notohara, Fausto Sessa, Carlo Capella, Stefano La Rosa, Sofia Asioli, Lizhi Zhang, Volkan Adsay, Francesca Franzi, Selenia Casnedi, Luca Albarello, Alessandro Vanoli, Alessandro Marando, La Rosa S, Adsay V, Albarello L, Asioli S, Casnedi S, Franzi F, Marando A, Notohara K, Sessa F, Vanoli A, Zhang L, and Capella C
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Male ,Pathology ,Perineural invasion ,Kaplan-Meier Estimate ,Japan ,Risk Factors ,morphology ,Nuclear atypia ,Lymph node ,acinar cell carcinoma ,Aged, 80 and over ,Middle Aged ,Prognosis ,Immunohistochemistry ,Tumor Burden ,Europe ,pancrea ,medicine.anatomical_structure ,Lymphatic Metastasis ,Female ,Anatomy ,Pancreas ,Pancreatic Acinar Cell Carcinoma ,Adult ,medicine.medical_specialty ,Risk Assessment ,Immunophenotyping ,Pathology and Forensic Medicine ,Necrosis ,Cytokeratin ,Predictive Value of Tests ,Biomarkers, Tumor ,medicine ,Carcinoma ,Acinar cell ,Humans ,Neoplasm Invasiveness ,Aged ,Cell Proliferation ,Neoplasm Staging ,Proportional Hazards Models ,Carcinoma, Acinar Cell ,business.industry ,Prognostic markers ,medicine.disease ,United States ,Pancreatic Neoplasms ,pancreas ,prognostic markers ,Multivariate Analysis ,Surgery ,business - Abstract
Acinar cell carcinoma (ACC) of the pancreas is a very rare tumor that has various morphologic features, which may give rise to diagnostic difficulties. Because of its rarity, many clinicopathologic characteristics remain to be further elucidated, and prognostic factors are yet to be well established. With the aim of better characterizing this carcinoma and searching for prognostic indicators, we collected 62 ACCs and investigated the following parameters: site, size, local infiltration, node and distant metastases, architectural pattern, nuclear atypia, presence of necrosis, lymphovascular and perineural invasion, proliferation, BCL10, trypsin, carboxyl ester lipase, amylase, lipase, PDX1, cytokeratin 19 (CK19), CK7, p53, and β-catenin expression. Twelve cases showing >30% of endocrine cells were reclassified as mixed acinar-neuroendocrine carcinomas, whereas 1 tumor was reclassified as a mixed ductal-acinar carcinoma and was excluded from the statistical prognostic evaluations. BCL10 and trypsin were the most reliable immunohistochemical markers, whereas amylase and lipase were not. Surgery was statistically correlated with a better prognosis (P=0.0008). Among resected tumors there was no difference in survival between ACCs and mixed acinar-neuroendocrine carcinomas, and factors that significantly correlated with poor prognosis were size >6.5 cm (P=0.004), lymph node (P=0.0039) and distant (P=0.008) metastases, and UICC stage (P=0.009). Stage was the only independent prognostic factor at multivariable analysis, and the best prognostic discrimination was observed on grouping together stages I and II and grouping together stages III and IV, suggesting a simplification of the UICC staging for such cancers. In addition, vascular and perineural invasion and CK19 and p53 expression showed a trend for poor prognosis, not reaching statistical significance.
- Published
- 2012
25. The effects of simulated monocular and binocular vision impairment on football penalty kick performance.
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Leivers HK, Allen PM, Timmis MA, Zenk F, Uppal J, and Runswick OR
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- Humans, Male, Young Adult, Adult, Vision Disorders physiopathology, Contrast Sensitivity physiology, Vision, Monocular physiology, Visual Fields physiology, Soccer physiology, Vision, Binocular physiology, Visual Acuity physiology, Athletic Performance physiology
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Sports performance is relatively robust under high levels of binocular blur. However, the limited research studies investigating monocular impairments has shown it has a larger impact on sport performance. This research study is relevant for classification in sports for athletes with vision impairment (VI), where visual acuity (VA) from the better eye is used during classification. Across two experiments, we aimed to establish the point at which binocular and monocular impairments affected performance in a football penalty kick (PK) through simulating varying severities of degraded VA and contrast sensitivity (CS) in active football players. In experiment one, 25 footballers performed PKs as VA and CS were systematically decreased in both eyes, and in one condition, visual field (VF) was reduced. The most severe VA/CS condition and reduced VF significantly impacted outcome, ball velocity and placement (ball kicked closer to the centre of the goal) (p < 0.05). In experiment two, 29 different footballers performed PKs as VA and CS of only the dominant eye were systematically decreased and in one condition the dominant eye was occluded, and participants viewed their environment through the non-dominant eye (monocular viewing). No differences were observed when assessing monocular impairments influence on outcome, velocity and ball placement. PKs have a high resilience to VI, but binocular impairment has a more immediate effect, suggesting binocular measures should be used in classification processes in football., (© 2024 The Author(s). European Journal of Sport Science published by Wiley‐VCH GmbH on behalf of European College of Sport Science.)
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- 2024
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26. Dual-Layer Spectral CT as Innovative Imaging Guidance in Lung Biopsies: Could Color-Coded Z-Effective Images Allow More Diagnostic Samplings and Biomarkers Information?
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Piacentino F, Fontana F, Zorzetto G, Saccomanno A, Gatta T, Recaldini C, Franzi F, Imperatori A, Rotolo N, Coppola A, Minenna M, Minici R, Ascenti V, Tripodi G, Bottari A, Laganà D, Ierardi AM, Carrafiello G, Sessa F, Carcano G, Ascenti G, and Venturini M
- Abstract
The aim of the study was to try to obtain more information on diagnostic samplings and biomarkers using dual-layer spectral CT in lung biopsies. Lung biopsies were performed by merging images obtained with CBCT with those from spectral CT to use them as functional guidance, experimenting with double sampling to determine the difference between the area with a higher Z-effective number and that with a lower Z-effective number. Ten patients with large lung lesions on spectral CT were selected and underwent percutaneous transthoracic lung mass biopsy. Technical success was calculated. The percentage of neoplastic, inflammatory, fibrotic, necrotic cells, or non-neoplastic lung parenchyma was reported. The possibility of carrying out immunohistochemical or molecular biology investigations was analyzed. All lesions were results malignant in 10/10 samples in the Z
max areas; in the Zmin areas, malignant cells were found in 7/10 samples. Technical success was achieved in 100% of cases for Zmax sampling and in 70% for Zmin sampling ( p -value: 0.2105). The biomolecular profile was detected in 9/10 (90%) cases in Zmax areas, while in 4/10 (40%) cases in Zmin areas ( p -value: 0.0573). The advantage of Z-effective imaging would be to identify a region of the lesion that is highly vascularized and probably richer in neoplastic cells, thus decreasing the risk of obtaining a non-diagnostic biopsy sample.- Published
- 2023
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27. Neuroendocrine Carcinoma of the Urinary Bladder: CT Findings and Radiomics Signature.
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Coppola A, Gatta T, Pini GM, Scordi G, Fontana F, Piacentino F, Minici R, Laganà D, Basile A, Dehò F, Carcano G, Franzi F, Uccella S, Sessa F, and Venturini M
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Background : We present a case series of Neuroendocrine Carcinoma of the Urinary Bladder (NECB) to analyse their radiologic appearance on CT, find a "Radiomic signature", and review the current literature. Methods : 14 CT cases of NECB were reviewed and compared with a control group of 42 patients with high-grade non-neuroendocrine bladder neoplasm for the following parameters: ring enhancement; implantation site; dimensions; density; margins; central necrosis; calcifications; number of lesions; wall thickness; depth of invasion in the soft tissue; invasion of fat tissue; invasion of adjacent organs; lymph-node involvement; abdominal organ metastasis. To extract radiomic features, volumes of interest of bladder lesions were manually delineated on the portal-venous phase. The radiomic features of the two groups were identified and compared. Results : Statistical differences among NECB and control group were found in the prevalence of male sex (100% vs. 69.0%), hydronephrosis (71.4% vs. 33.3%), mean density of the mass (51.01 ± 15.48 vs. 76.27 ± 22.26 HU); product of the maximum diameters on the axial plane (38.1 ± 59.3 vs. 14.44 ± 12.98 cm2) in the control group, trigonal region involvement (78.57% vs. 19.05%). About the radiomic features, Student's t -test showed significant correlation for the variables: "DependenceNonUniformity" ( p : 0.048), "JointAverage" ( p : 0.013), "LargeAreaLowGrayLevelEmphasis" ( p : 0.014), "Maximum2DDiameterColumn" ( p : 0.04), "Maximum 2DDiameterSlice" ( p : 0.007), "MeanAbsoluteDeviation" ( p : 0.021), "BoundingBoxA" ( p : 0.022) and "CenterOfMassB" ( p : 0.007). Conclusions : There is a typical pattern (male patient, large mass, trigonal area involvement) of NECB presentation on contrast-enhanced CT. Certain morphological characteristics and encouraging results about Radiomic features can help define the diagnosis.
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- 2023
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28. Could Maximum SUV be Used as Imaging Guidance in Large Lung Lesions Biopsies? Double Sampling Under PET-CT/XperGuide Fusion Imaging in Inhomogeneous Lung Uptaking Lesions to Show That it can Make a Difference.
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Piacentino F, Fontana F, Zorzetto G, Saccomanno A, Casagrande S, Franzi F, Imperatori A, Lanza C, Carriero S, Coppola A, Ierardi AM, Carrafiello G, and Venturini M
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- Humans, Positron Emission Tomography Computed Tomography methods, Retrospective Studies, Lung diagnostic imaging, Lung pathology, Positron-Emission Tomography, Biopsy, Inflammation pathology, Fluorodeoxyglucose F18, Neoplasms pathology, Lung Neoplasms diagnostic imaging, Lung Neoplasms pathology
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Introduction: The purpose of this study is to evaluate the diagnostic value of positron emission computed tomography-cone beam computed tomography (PET/CT-CBCT) fusion guided percutaneous biopsy, targeted to the maximum standardized uptake value (SUVmax) and minimum standardized uptake value (SUVmin) of large lung lesions. Materials and Methods: Inside a larger cohort of PET/CT-CBCT guided percutaneous lung biopsies, 10 patients with large pulmonary lesions (diameter > 30 mm) were selected retrospectively. These patients have been subjected to double biopsy sampling respectively in the SUVmax area and in the SUVmin area of the lesion. Technical success has been calculated. For each sample, the percentage of neoplastic, inflammatory, and fibrotic cells was reported. Furthermore, the possibility of performing immunohistochemical or molecular biology investigations to specifically define the biomolecular tumor profile was analyzed. Results: Nine lesions were found to be malignant, one benign (inflammation). Technical success was 100% (10/10) in the SUVmax samples and 70% (7/10) in the SUVmin samples ( P-value: .21 ). In the first group, higher percentages of neoplastic cells were found at pathologic evaluation, while in the second group areas of inflammation and fibrosis were more represented. The biomolecular profile was obtained in 100% of cases (9/9) of the first group, while in the second group only in 33.3% of cases (2/6), with a statistically significant difference between the 2 groups ( P-value: .011 ). Conclusion: A correlation between the standardized uptake value value and the technical success of the biopsy sample has been identified. PET/CT-CBCT guidance allows to target the biopsy in the areas of the tumor which are richer in neoplastic cells, thus obtaining more useful information for the planning of patient-tailored cancer treatments.
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- 2023
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29. Biphenotypic sinonasal sarcoma: European multicentre case-series and systematic literature review.
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Turri-Zanoni M, Dalfino G, Lechner M, Dallan I, Battaglia P, Facco C, Franzi F, Gravante G, Ferrari M, Terzakis D, Jay A, Forster MD, Ambrosoli AL, Bignami M, Georgalas C, Herman P, Nicolai P, Lund VJ, and Castelnuovo P
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- Humans, Disease-Free Survival, Retrospective Studies, Multicenter Studies as Topic, Paranasal Sinus Neoplasms surgery, Sarcoma pathology
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Objective: Biphenotypic sinonasal sarcoma (BSNS) is a rare low-grade cancer that was included from the 4th edition of WHO classification of head and neck tumours. The purpose of this study is to analyse clinical behaviour, pattern of recurrences and survival outcomes of this neoplasm., Methods: Retrospective review of patients affected by BSNS who were treated via an endoscopic-assisted approach in 6 European tertiary-care referral hospitals. Cases of BSNS described in literature since 2012 to date were fully reviewed, according to PRISMA guidelines., Results: A total of 15 patients were included. Seven patients were treated via an endoscopic endonasal approach, 4 with endoscopic transnasal craniectomy, and 4 via a cranio-endoscopic approach. Adjuvant treatment was delivered in 2 cases. After a mean follow-up of 27.3 months, systemic metastasis was observed in 1 case; the 5-year overall survival and disease-free survival rates were 100% and 80 ± 17.9%, respectively., Conclusions: BSNS is a locally aggressive tumour with a low recurrence rate and encouraging survival outcomes if properly treated with surgical resection and free margins followed by adjuvant radiotherapy for selected cases. Endoscopic-assisted surgery is safe and effective as an upfront treatment within a multidisciplinary care protocol., (Copyright © 2022 Società Italiana di Otorinolaringoiatria e Chirurgia Cervico-Facciale, Rome, Italy.)
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- 2022
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30. Surgical management of tracheal chondrosarcoma.
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Rotolo N, Cattoni M, Nardecchia E, De Maio S, Franzi F, Pettenon F, and Imperatori A
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- Aged, Anastomosis, Surgical, Endoscopy, Humans, Male, Middle Aged, Bone Neoplasms surgery, Chondrosarcoma surgery, Tracheal Neoplasms diagnosis, Tracheal Neoplasms surgery
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Background: Tracheal chondrosarcoma is an extremely rare, slow-growing, malignant tumour. This study aims to analyze the cases of tracheal chondrosarcoma published in the literature and our case report, in order to better define tracheal chondrosarcoma management. Methods: A systematic review of the English literature was carried out for fully described tracheal chondrosarcoma cases. Additionally, we reported a new case of a 58-year-old man undergoing tracheal resection and reconstruction for tracheal chondrosarcoma. Results: To date, 30 cases were published. This tumour predominantly involved male patients (93%; median age: 65 years), generally conditioning dyspnoea and cough. Most of the patients underwent tracheal resection with end-to-end anastomosis, without recurrence (median follow-up: 2 years). Tumours endoscopically treated recurred in half cases. Conclusion: Tracheal resection is the treatment of choice for chondrosarcoma, with an excellent prognosis. Endoscopic treatment and/or radiotherapy should be indicated for patients unfit for surgery.
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- 2022
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31. Prognostic role of standard uptake value according to pathologic features of lung adenocarcinoma.
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Bertoglio P, Ventura L, Aprile V, Cattoni MA, Nachira D, Lococo F, Rodriguez Perez M, Guerrera F, Minervini F, Gnetti L, Bacchin D, Franzi F, Querzoli G, Rindi G, Bellafiore S, Femia F, Viti A, Kestenholz P, Ruffini E, Paci M, Margaritora S, Imperatori AS, Lucchi M, Carbognani P, and Terzi AC
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- Fluorodeoxyglucose F18, Humans, Neoplasm Staging, Positron Emission Tomography Computed Tomography, Positron-Emission Tomography, Prognosis, Retrospective Studies, Adenocarcinoma of Lung pathology, Adenocarcinoma of Lung surgery, Lung Neoplasms pathology
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Objective: To evaluate the influence of lung adenocarcinoma second predominant pattern on the maximal standard uptake value (SUVmax) and its prognostic effect in different histologic groups., Methods: We retrospectively collected surgically resected pathologic stage I and II lung adenocarcinoma from nine European institutions. Only patients who underwent preoperative PET-CT and with available information regarding SUVmax of T (SUVmaxT) and N1 (SUVmaxN1) component were included., Results: We enrolled 344 patients with lung adenocarcinoma. SUVmaxT did not show any significant relation according to the second predominant pattern ( p = 0.139); this relationship remained nonsignificant in patients with similar predominant pattern. SUVmaxT influenced the disease-free survival in the whole cohort ( p = 0.002) and in low- and intermediate-grade predominant pattern groups ( p = 0.040 and p = 0.008, respectively). In the high-grade predominant pattern cohort and in the pathologic N1 cases, SUVmaxT lost its prognostic power. SUVmaxN1 did not show any significant correlation with predominant and second predominant patterns and did not have any prognostic impact on DFS., Conclusions: SUVmaxT is influenced only by the adenocarcinoma predominant pattern, but not by second predominant pattern. Concurrently, in high-grade predominant pattern and pN1 group the prognostic power of SUVmaxT becomes nonsignificant.
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- 2022
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32. Impact of High-Grade Patterns in Early-Stage Lung Adenocarcinoma: A Multicentric Analysis.
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Bertoglio P, Aprile V, Ventura L, Cattoni M, Nachira D, Lococo F, Perez MR, Guerrera F, Minervini F, Querzoli G, Bocchialini G, Bacchin D, Franzi F, Rindi G, Bellafiore S, Femia F, Bogina GS, Solli P, Kestenholz P, Ruffini E, Paci M, Margaritora S, Imperatori AS, Lucchi M, Gnetti L, and Terzi AC
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- Female, Humans, Male, Neoplasm Recurrence, Local pathology, Neoplasm Staging, Prognosis, Retrospective Studies, Adenocarcinoma pathology, Adenocarcinoma surgery, Adenocarcinoma of Lung pathology, Adenocarcinoma of Lung surgery, Lung Neoplasms pathology
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Objective: The presence of micropapillary and solid adenocarcinoma patterns leads to a worse survival and a significantly higher tendency to recur. This study aims to assess the impact of pT descriptor combined with the presence of high-grade components on long-term outcomes in early-stage lung adenocarcinomas., Methods: We retrospectively collected data of consecutive resected pT1-T3N0 lung adenocarcinoma from nine European Thoracic Centers. All patients who underwent a radical resection with lymph-node dissection between 2014 and 2017 were included. Differences in Overall Survival (OS) and Disease-Free Survival (DFS) and possible prognostic factors associated with outcomes were evaluated also after performing a propensity score matching to compare tumors containing non-high-grade and high-grade patterns., Results: Among 607 patients, the majority were male and received a lobectomy. At least one high-grade histological pattern was seen in 230 cases (37.9%), of which 169 solid and 75 micropapillary. T1a-b-c without high-grade pattern had a significant better prognosis compared to T1a-b-c with high-grade pattern (p = 0.020), but the latter had similar OS compared to T2a (p = 0.277). Concurrently, T1a-b-c without micropapillary or solid patterns had a significantly better DFS compared to those with high-grade patterns (p = 0.034), and it was similar to T2a (p = 0.839). Multivariable analysis confirms the role of T descriptor according to high-grade pattern both for OS (p = 0.024; HR 1.285 95% CI 1.033-1.599) and DFS (p = 0.003; HR 1.196, 95% CI 1.054-1.344, respectively). These results were confirmed after the propensity score matching analysis., Conclusions: pT1 lung adenocarcinomas with a high-grade component have similar prognosis of pT2a tumors., (© 2022. The Author(s).)
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- 2022
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33. Pathological and clinical features of multiple cancers and lung adenocarcinoma: a multicentre study.
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Bertoglio P, Ventura L, Aprile V, Cattoni MA, Nachira D, Lococo F, Rodriguez Perez M, Guerrera F, Minervini F, Gnetti L, Lenzini A, Franzi F, Querzoli G, Rindi G, Bellafiore S, Femia F, Bogina GS, Bacchin D, Kestenholz P, Ruffini E, Paci M, Margaritora S, Imperatori AS, Lucchi M, Ampollini L, and Terzi AC
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- Humans, Male, Neoplasm Staging, Prognosis, Retrospective Studies, Adenocarcinoma pathology, Adenocarcinoma of Lung pathology, Lung Neoplasms diagnosis, Lung Neoplasms epidemiology, Lung Neoplasms surgery
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Objectives: Lung cancer is increasingly diagnosed as a second cancer. Our goal was to analyse the characteristics and outcomes of early-stage resected lung adenocarcinomas in patients with previous cancers (PC) and correlations with adenocarcinoma subtypes., Methods: We retrospectively reviewed data of patients radically operated on for stage I-II lung adenocarcinoma in 9 thoracic surgery departments between 2014 and 2017. Overall survival (OS) and time to disease relapse were evaluated between subgroups., Results: We included 700 consecutive patients. PC were present in 260 (37.1%). Breast adenocarcinoma, lung cancer and prostate cancer were the most frequent (21.5%, 11.5% and 11.2%, respectively). No significant differences in OS were observed between the PC and non-PC groups (P = 0.378), with 31 and 75 deaths, respectively. Patients with PC had smaller tumours and were more likely to receive sublobar resection and to be operated on with a minimally invasive approach. Previous gastric cancer (P = 0.042) and synchronous PC (when diagnosed up to 6 months before lung adenocarcinoma; P = 0.044) were related, with a worse OS. Colon and breast adenocarcinomas and melanomas were significantly related to a lower incidence of high grade (solid or micropapillary, P = 0.0039, P = 0.005 and P = 0.028 respectively), whereas patients affected by a previous lymphoma had a higher incidence of a micropapillary pattern (P = 0.008)., Conclusions: In patients with PC, we found smaller tumours more frequently treated with minimally invasive techniques and sublobar resection, probably due to a more careful follow-up. The impact on survival is not uniform and predictable; however, breast and colon cancers and melanoma showed a lower incidence of solid or micropapillary patterns whereas patients with lymphomas had a higher incidence of a micropapillary pattern., (© The Author(s) 2022. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery.)
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- 2022
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34. Prognostic impact of lung adenocarcinoma second predominant pattern from a large European database.
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Bertoglio P, Querzoli G, Ventura L, Aprile V, Cattoni MA, Nachira D, Lococo F, Rodriguez Perez M, Guerrera F, Minervini F, Gnetti L, Bacchin D, Franzi F, Rindi G, Bellafiore S, Femia F, Viti A, Bogina GS, Kestenholz P, Ruffini E, Paci M, Margaritora S, Imperatori AS, Lucchi M, Ampollini L, and Terzi AC
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- Adenocarcinoma of Lung surgery, Adenocarcinoma, Papillary surgery, Aged, Carcinoma, Acinar Cell surgery, Europe, Female, Follow-Up Studies, Humans, Lung Neoplasms surgery, Male, Neoplasm Recurrence, Local surgery, Prognosis, Retrospective Studies, Survival Rate, Adenocarcinoma of Lung pathology, Adenocarcinoma, Papillary pathology, Carcinoma, Acinar Cell pathology, Databases, Factual, Lung Neoplasms pathology, Neoplasm Recurrence, Local pathology
- Abstract
Background and Objectives: Adenocarcinoma patterns could be grouped based on clinical behaviors: low- (lepidic), intermediate- (papillary or acinar), and high-grade (micropapillary and solid). We analyzed the impact of the second predominant pattern (SPP) on disease-free survival (DFS)., Methods: We retrospectively collected data of surgically resected stage I and II adenocarcinoma., Selection Criteria: anatomical resection with lymphadenectomy and pathological N0. Pure adenocarcinomas and mucinous subtypes were excluded. Recurrence rate and factors affecting DFS were analyzed according to the SPP focusing on intermediate-grade predominant pattern adenocarcinomas., Results: Among 270 patients, 55% were male. The mean age was 68.3 years. SPP pattern appeared as follows: lepidic 43.0%, papillary 23.0%, solid 14.4%, acinar 11.9%, and micropapillary 7.8%. The recurrence rate was 21.5% and 5-year DFS was 71.1%. No difference in DFS was found according to SPP (p = .522). In patients with high-grade SPP, the percentage of SPP, age, and tumor size significantly influenced DFS (p = .016). In patients with lepidic SPP, size, male gender, and lymph-node sampling (p = .005; p = .014; p = .038, respectively) significantly influenced DFS., Conclusions: The impact of SPP on DFS is not homogeneous in a subset of patients with the intermediate-grade predominant patterns. The influence of high-grade SPP on DFS is related to its proportion in the tumor., (© 2020 Wiley Periodicals LLC.)
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- 2021
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35. Beta1- and Beta2-Adrenoceptors Expression Patterns in Human Non-small Cell Lung Cancer: Relationship with Cancer Histology.
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Coelho M, Imperatori A, Chiaravalli AM, Franzi F, Castiglioni M, Rasini E, Luini A, Legnaro M, Marino F, Ribeiro L, and Cosentino M
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- A549 Cells, Adrenergic beta-1 Receptor Agonists pharmacology, Adrenergic beta-2 Receptor Agonists pharmacology, Aged, Biomarkers, Tumor biosynthesis, Biomarkers, Tumor genetics, Carcinoma, Non-Small-Cell Lung genetics, Carcinoma, Non-Small-Cell Lung pathology, Dose-Response Relationship, Drug, Female, Humans, Lung Neoplasms genetics, Lung Neoplasms pathology, Male, Middle Aged, Receptors, Adrenergic, beta-1 genetics, Receptors, Adrenergic, beta-2 genetics, Retrospective Studies, S Phase drug effects, S Phase physiology, Carcinoma, Non-Small-Cell Lung metabolism, Gene Expression Regulation, Enzymologic drug effects, Lung Neoplasms metabolism, Receptors, Adrenergic, beta-1 biosynthesis, Receptors, Adrenergic, beta-2 biosynthesis
- Abstract
Assessment of Beta-AR protein expression on tumour tissues might be a plausible strategy to select cancer patients who can benefit from Beta-blockers therapy. The aim of this study is to evaluate the differences between resected tissue specimens from primary lung cancer (adenocarcinoma (ADC) and squamous cell carcinoma (SCC)) in terms of expression pattern of Beta1- and Beta2-AR in both tumour and adjacent surrounding non-tumour tissue. This retrospective study was based on the analysis of 80 patients with histologically confirmed diagnosis of primary Non-Small Cell Lung Cancer (NSCLC) who received surgical treatment. The cases were carefully selected in order to obtain the most homogeneous sample in terms of histologic subtype (40 ADCs and 40 SCCs) and clinical stage (10 each). Beta1- and Beta2-AR expression was determined by immunohistochemistry and the staining evaluated by semi-quantitative scoring using the H-score method. In our NSCLC series, Beta1- and Beta2-AR are differentially expressed. Beta1-AR expression is present at low levels in both SCC and ADC. Likewise, when compared with the matched surrounding non-tumour tissues, Beta1-AR expression level was significantly lower in both histologic subtypes. Conversely, Beta2-AR is highly expressed in both histologic subtypes, but clearly highly expressed in ADC when compared with SCC and with their matched surrounding non-tumour tissue. Overall, this clinicopathological study highlights the differential expression of Beta1- and Beta2-AR in ADC and SCC. Repurposing non-selective Beta-blockers in oncologic setting might be a suitable therapeutic strategy for lung ADC. Graphical abstract.
- Published
- 2019
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36. LINE-1 hypomethylation is associated to specific clinico-pathological features in Stage I non-small cell lung cancer.
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Imperatori A, Sahnane N, Rotolo N, Franzi F, Nardecchia E, Libera L, Romualdi C, Cattoni M, Sessa F, Dominioni L, and Furlan D
- Subjects
- Aged, Aged, 80 and over, Biomarkers, Tumor, Carcinoma, Non-Small-Cell Lung mortality, Carcinoma, Non-Small-Cell Lung therapy, DNA Mutational Analysis, Epigenesis, Genetic, Female, Follow-Up Studies, Genetic Association Studies, Humans, Lung Neoplasms mortality, Lung Neoplasms therapy, Male, Middle Aged, Neoplasm Grading, Neoplasm Staging, Prognosis, Smoking, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Survival Analysis, Carcinoma, Non-Small-Cell Lung diagnosis, Carcinoma, Non-Small-Cell Lung genetics, DNA Methylation, Long Interspersed Nucleotide Elements, Lung Neoplasms diagnosis, Lung Neoplasms genetics
- Abstract
Objectives: We hypothesize that selected genetic and/or epigenetic changes associated with advanced tumours may help identifying early non-small cell lung cancers (NSCLCs) that recur after resection. Among epigenetic changes, long interspersed nuclear element-1 (LINE-1) hypomethylation is seen early during carcinogenesis and may act in concert with genetic alterations to cancer progression. LINE-1 hypomethylation and gene mutations frequently involved in lung cancer, were analysed to evaluate their prognostic role in resected stage I NSCLC., Methods: Gene mutations and LINE-1 methylation were analysed in 167 Caucasian patients with stage I NSCLC, namely 100 adenocarcinomas (ADC) and 67 squamous-cell carcinomas (SqCC), using mass-spectrometry and pyrosequencing. We evaluated the correlation between molecular results and clinico-pathological data: age, gender, smoking status, period of surgery, histology, grading, pathological stage, p53 expression, LINE-1 hypomethylation. These variables have been assessed as possible predictors of cancer related survival by regression analysis., Results: Frequency and spectrum of gene mutations were significantly different in ADCs compared with SqCCs. p53 positivity was more common in SqCC, while EGFR or KRAS mutations were mainly detected in ADC. LINE1 hypomethylation was associated with SqCC histology, p53 immunoreactivity and smoking habit. Stage IB, LINE-1 hypomethylation and PIK3CA mutation independently predicted a worse cancer-related survival. When combined into a scoring system, their prognostic power was strengthened., Conclusions: In many stage I NSCLC a mutation pattern of advanced disease was observed. Stage IB, LINE-1 hypomethylation and PIK3CA mutation were associated to poor prognosis. Genetic and epigenetic events occurring in early carcinogenesis may help identifying stage I NSCLC patients who deserve adjuvant therapy., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2017
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37. Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA)-from morphology to molecular testing.
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Righi L, Franzi F, Montarolo F, Gatti G, Bongiovanni M, Sessa F, and La Rosa S
- Abstract
In recent years, endobronchial ultrasound-guided TBNA (EBUS-TBNA) has emerged as an innovative technique for diagnosis and staging of lung cancer and has been successfully introduced into daily clinical practice with several advantages including minimally invasive approach, safe, cost-effective, real time image guidance, broad sampling capability, and rapid on-site evaluation (ROSE). Both cytological and histological approach could be useful to have material for diagnosis, immunohistochemical and molecular analyses which may be very important for targeted therapy with successful rate ranging from 89% to 98%. The utility of ROSE during EBUS-TBNA has been matter of debate. Indeed, although some evidence concluded that ROSE does not increase the diagnostic efficacy of EBUS-TBNA, other demonstrated that it improves the diagnostic yield of the procedure up to 30%, allows to avoid repetition of additional diagnostic procedures and reduces risk of complications. Furthermore the sample preparation by cytopathologist is optimized with the aid of direct macroscopic inspection, optimal smearing techniques, and triage of the sample permitting to obtain adequate tissue for diagnosis, ancillary techniques and molecular testing, when needed. Some pathological issues on EBUS-TBNA are reviewed and discussed with particular focus on ROSE and molecular testing., Competing Interests: Conflicts of Interest: The authors have no conflicts of interest to declare.
- Published
- 2017
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38. Pyrosequencing for EGFR mutation detection: diagnostic accuracy and clinical implications.
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Sahnane N, Gueli R, Tibiletti MG, Bernasconi B, Stefanoli M, Franzi F, Pinotti G, Capella C, and Furlan D
- Subjects
- Adult, Aged, Aged, 80 and over, Antineoplastic Agents therapeutic use, Carcinoma, Non-Small-Cell Lung drug therapy, Enzyme Inhibitors therapeutic use, Female, Humans, Male, Middle Aged, Retrospective Studies, Treatment Outcome, ErbB Receptors genetics, Mutation, Pathology, Molecular methods, Sequence Analysis, DNA methods
- Abstract
EGFR-activating mutations predict responsiveness to EGFR tyrosine kinase inhibitors (TKIs) in non-small cell lung cancer (NSCLC) patients. Mutation screening is crucial to support therapeutic decisions and is commonly conducted using dideoxy sequencing, although its sensitivity is suboptimal in clinical settings. To evaluate the diagnostic performance of pyrosequencing and dideoxy sequencing, we examined EGFR mutation status in a retrospective cohort of 53 patients with NSCLCs clinically selected for TKI therapy and whose clinical outcome was available. Moreover, pyrosequencing quantitative results were compared with EGFR amplification data. EGFR mutations were investigated by pyrosequencing and by dideoxy sequencing. Detection rates of both methods were determined by titration assays using NCI-H1975 and HCC-827 cell lines. Increased EGFR copy number was assessed by fluorescence in situ hybridization (FISH). Pyrosequencing showed a higher detection rate than dideoxy sequencing. Tumor control rate of cases with mutant and wild-type EGFR was 86% and 29%, respectively. EGFR amplification was significantly associated with EGFR mutation and a positive correlation between high percentages of mutant alleles and clinical response to TKI was observed. We concluded that pyrosequencing is more sensitive than dideoxy sequencing in mutation screening for EGFR mutations. Detection rate of dideoxy sequencing was suboptimal when low frequencies of mutant alleles or low tumor cell contents were observed. Pyrosequencing enables quantification of mutant alleles that correlates well with increased EGFR copy number assessed by FISH. Pyrosequencing should be used in molecular diagnostic of NSCLC to appropriately select patients who are likely to benefit from TKI therapy.
- Published
- 2013
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39. Mixed exocrine-neuroendocrine carcinoma of the nasal cavity: clinico-pathologic and molecular study of a case and review of the literature.
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La Rosa S, Furlan D, Franzi F, Battaglia P, Frattini M, Zanellato E, Marando A, Sahnane N, Turri-Zanoni M, Castelnuovo P, and Capella C
- Subjects
- Adenocarcinoma genetics, Adenocarcinoma metabolism, Adenocarcinoma pathology, Aged, Biomarkers, Tumor analysis, Carcinoma, Neuroendocrine genetics, Carcinoma, Neuroendocrine metabolism, Carcinoma, Neuroendocrine pathology, DNA Mutational Analysis, Humans, Immunohistochemistry, Male, Neoplasms, Complex and Mixed genetics, Neoplasms, Complex and Mixed metabolism, Nose Neoplasms genetics, Nose Neoplasms metabolism, Nasal Cavity pathology, Neoplasms, Complex and Mixed pathology, Nose Neoplasms pathology
- Abstract
Sinonasal intestinal-type adenocarcinomas (ITACs) are rare neoplasms histologically resembling intestinal adenocarcinomas. Although a neuroendocrine differentiation in ITACs has been described, true mixed exocrine-neuroendocrine carcinomas, neoplasms in which each component represents at least 30 % of the lesion, are extremely rare and their molecular alterations are largely unknown. We describe herein the clinico-pathologic features, the methylation profile, chromosomal gains and losses, and mutation analysis of KRAS, BRAF and p53 in a nasal mixed exocrine-neuroendocrine carcinoma resected in a 79-year-old man. The tumor was composed of an ITAC and a poorly differentiated neuroendocrine carcinoma. Both exocrine and neuroendocrine components were CK8, CK20, CDX2 and p53 positive, and CK7 and TTF1 negative. The neuroendocrine component also showed immunoreactivity for chromogranin A, synaptophysin, serotonin and glicentin. Gains and losses were found at following chromosome regions: 17p13 (TP53), 14q24 (MLH3), 19q13 (KLK3), 5q21 (APC), 7q21 (CDK6), 9q34 (DAPK1), 12p13 (TNFRSF 1A, CDKN1B), 13q12 (BRCA2), 17p13.3 (HIC1), 18q21 (BCL2), and 22q12 (TIMP3). Aberrant methylation was detected only in the neuroendocrine component and involved APC and DAPK1 genes. No mutation of KRAS (exons 2-4), BRAF (exon 15), and p53 (exons 4-10) was found in both components. The results suggest a monoclonal origin of the tumor from a pluripotent cell undergoing a biphenotypic differentiation and that the neuroendocrine differentiation may be from an exocrine to an endocrine pathway. We have also reviewed the literature on sinonasal mixed exocrine-neuroendocrine carcinomas to give to the reader a comprehensive overview of these very rare tumor types.
- Published
- 2013
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40. The proangiogenic phenotype of natural killer cells in patients with non-small cell lung cancer.
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Bruno A, Focaccetti C, Pagani A, Imperatori AS, Spagnoletti M, Rotolo N, Cantelmo AR, Franzi F, Capella C, Ferlazzo G, Mortara L, Albini A, and Noonan DM
- Subjects
- Aged, Carcinoma, Non-Small-Cell Lung metabolism, Carcinoma, Non-Small-Cell Lung pathology, Female, Humans, Immunity, Innate genetics, Killer Cells, Natural cytology, Lung Neoplasms metabolism, Lung Neoplasms pathology, Male, Middle Aged, Neoplasm Staging, Transforming Growth Factor beta1 immunology, Tumor Microenvironment immunology, Carcinoma, Non-Small-Cell Lung immunology, Killer Cells, Natural immunology, Lung Neoplasms immunology, Neovascularization, Pathologic genetics, Neovascularization, Pathologic immunology, Transforming Growth Factor beta1 metabolism
- Abstract
The tumor microenvironment can polarize innate immune cells to a proangiogenic phenotype. Decidual natural killer (dNK) cells show an angiogenic phenotype, yet the role for NK innate lymphoid cells in tumor angiogenesis remains to be defined. We investigated NK cells from patients with surgically resected non-small cell lung cancer (NSCLC) and controls using flow cytometric and functional analyses. The CD56(+)CD16(-) NK subset in NSCLC patients, which represents the predominant NK subset in tumors and a minor subset in adjacent lung and peripheral blood, was associated with vascular endothelial growth factor (VEGF), placental growth factor (PIGF), and interleukin-8 (IL-8)/CXCL8 production. Peripheral blood CD56(+)CD16(-) NK cells from patients with the squamous cell carcinoma (SCC) subtype showed higher VEGF and PlGF production compared to those from patients with adenocarcinoma (AdC) and controls. Higher IL-8 production was found for both SCC and AdC compared to controls. Supernatants derived from NSCLC CD56(+)CD16(-) NK cells induced endothelial cell chemotaxis and formation of capillary-like structures in vitro, particularly evident in SCC patients and absent from controls. Finally, exposure to transforming growth factor-β(1) (TGFβ(1)), a cytokine associated with dNK polarization, upregulated VEGF and PlGF in peripheral blood CD56(+)CD16(-) NK cells from healthy subjects. Our data suggest that NK cells in NSCLC act as proangiogenic cells, particularly evident for SCC and in part mediated by TGFβ(1).
- Published
- 2013
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41. Clinicopathologic study of 62 acinar cell carcinomas of the pancreas: insights into the morphology and immunophenotype and search for prognostic markers.
- Author
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La Rosa S, Adsay V, Albarello L, Asioli S, Casnedi S, Franzi F, Marando A, Notohara K, Sessa F, Vanoli A, Zhang L, and Capella C
- Subjects
- Adult, Aged, Aged, 80 and over, Carcinoma, Acinar Cell chemistry, Carcinoma, Acinar Cell immunology, Carcinoma, Acinar Cell mortality, Carcinoma, Acinar Cell secondary, Carcinoma, Acinar Cell surgery, Cell Proliferation, Europe, Female, Humans, Immunohistochemistry, Japan, Kaplan-Meier Estimate, Lymphatic Metastasis, Male, Middle Aged, Multivariate Analysis, Necrosis, Neoplasm Invasiveness, Neoplasm Staging, Pancreatic Neoplasms chemistry, Pancreatic Neoplasms immunology, Pancreatic Neoplasms mortality, Pancreatic Neoplasms pathology, Pancreatic Neoplasms surgery, Predictive Value of Tests, Prognosis, Proportional Hazards Models, Risk Assessment, Risk Factors, Tumor Burden, United States, Biomarkers, Tumor analysis, Carcinoma, Acinar Cell diagnosis, Immunophenotyping, Pancreatic Neoplasms diagnosis
- Abstract
Acinar cell carcinoma (ACC) of the pancreas is a very rare tumor that has various morphologic features, which may give rise to diagnostic difficulties. Because of its rarity, many clinicopathologic characteristics remain to be further elucidated, and prognostic factors are yet to be well established. With the aim of better characterizing this carcinoma and searching for prognostic indicators, we collected 62 ACCs and investigated the following parameters: site, size, local infiltration, node and distant metastases, architectural pattern, nuclear atypia, presence of necrosis, lymphovascular and perineural invasion, proliferation, BCL10, trypsin, carboxyl ester lipase, amylase, lipase, PDX1, cytokeratin 19 (CK19), CK7, p53, and β-catenin expression. Twelve cases showing >30% of endocrine cells were reclassified as mixed acinar-neuroendocrine carcinomas, whereas 1 tumor was reclassified as a mixed ductal-acinar carcinoma and was excluded from the statistical prognostic evaluations. BCL10 and trypsin were the most reliable immunohistochemical markers, whereas amylase and lipase were not. Surgery was statistically correlated with a better prognosis (P=0.0008). Among resected tumors there was no difference in survival between ACCs and mixed acinar-neuroendocrine carcinomas, and factors that significantly correlated with poor prognosis were size >6.5 cm (P=0.004), lymph node (P=0.0039) and distant (P=0.008) metastases, and UICC stage (P=0.009). Stage was the only independent prognostic factor at multivariable analysis, and the best prognostic discrimination was observed on grouping together stages I and II and grouping together stages III and IV, suggesting a simplification of the UICC staging for such cancers. In addition, vascular and perineural invasion and CK19 and p53 expression showed a trend for poor prognosis, not reaching statistical significance.
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- 2012
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42. Serotonin-producing enterochromaffin cell tumors of the pancreas: clinicopathologic study of 15 cases and comparison with intestinal enterochromaffin cell tumors.
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La Rosa S, Franzi F, Albarello L, Schmitt A, Bernasconi B, Tibiletti MG, Finzi G, Placidi C, Perren A, and Capella C
- Subjects
- Adult, Aged, Chromosomes, Human, Pair 18 genetics, Female, Humans, In Situ Hybridization, Fluorescence, Intestinal Neoplasms genetics, Kaplan-Meier Estimate, Male, Malignant Carcinoid Syndrome genetics, Malignant Carcinoid Syndrome metabolism, Malignant Carcinoid Syndrome pathology, Microscopy, Electron, Transmission, Middle Aged, Pancreatic Neoplasms genetics, Carcinoid Tumor metabolism, Carcinoid Tumor pathology, Enterochromaffin Cells metabolism, Enterochromaffin Cells pathology, Intestinal Neoplasms metabolism, Intestinal Neoplasms pathology, Pancreatic Neoplasms metabolism, Pancreatic Neoplasms pathology, Serotonin biosynthesis
- Abstract
Objectives: Serotonin-producing tumors of the pancreas are rare endocrine neoplasms composed of enterochromaffin (EC) cells that have been mainly described in the literature as case reports. This study analyzes the clinicopathologic features of a series of pancreatic EC cell neoplasms and their similarities to and differences from intestinal EC cell tumors., Methods: The morphological, immunohistochemical, ultrastructural, and fluorescent in situ hybridization features of 15 pancreatic and 20 intestinal serotonin-producing neoplasms were compared. In addition, we reviewed the literature on pancreatic serotonin-producing tumors to better understand the clinicopathologic features of this rare tumor type., Results: The lack of substance P and acidic fibroblast growth factor immunoreactivity; the low immunohistochemical expression of CDX2, vesicular monoamine transporter 1, connective tissue growth factor, and prostatic acid phosphatase; the lack of S100-positive sustentacular cells; the strong expression of vesicular monoamine transporter 2; and peculiar ultrastructural features characterize pancreatic EC cell tumors and differentiate them from intestinal ones, although both categories show similar chromosome 18 cytogenetic alterations. The review of the literature indicates that pancreatic functioning tumors associated with the carcinoid syndrome arise in younger patients and are larger, more frequently malignant, and more aggressive neoplasms than pancreatic nonfunctioning ones., Conclusions: Pancreatic EC cell tumors show several different morphological features compared with related intestinal tumors despite similar cytogenetic alterations on chromosome 18.
- Published
- 2011
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43. Ectopic congenital thymic cyst in the right pleural cavity.
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Bruno VD, Mariscalco G, Franzi F, Miceli A, Piffaretti G, and Sala A
- Subjects
- Adult, Biopsy, Choristoma surgery, Humans, Male, Mediastinal Cyst congenital, Mediastinal Cyst surgery, Pleural Diseases surgery, Radiography, Thoracic, Thoracotomy, Tomography, X-Ray Computed, Treatment Outcome, Choristoma diagnosis, Mediastinal Cyst diagnosis, Pleural Diseases diagnosis
- Abstract
A 37-year-old man with a huge pleural cyst, presented with symptoms of right heart compression. The mass on the right side of the chest seemed initially to be in connection with the mediastinum. Computed tomography failed to define its relationship with the pericardium, and echocardiography excluded any involvement of the mediastinal structures. The final diagnosis was a congenital thymic cyst exclusively located in the pleural cavity.
- Published
- 2010
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44. Osteopontin is not a specific marker in malignant pleural mesothelioma.
- Author
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Paleari L, Rotolo N, Imperatori A, Puzone R, Sessa F, Franzi F, Meacci E, Camplese P, Cesario A, and Paganuzzi M
- Subjects
- Adult, Aged, Aged, 80 and over, Disease Progression, Female, Humans, Male, Middle Aged, Neoplasm Metastasis, Treatment Outcome, Biomarkers, Tumor metabolism, Lung Neoplasms diagnosis, Lung Neoplasms metabolism, Mesothelioma diagnosis, Mesothelioma metabolism, Osteopontin biosynthesis, Pleural Neoplasms diagnosis, Pleural Neoplasms metabolism
- Abstract
Background and Aims: Osteopontin (OPN) is an integrin-binding protein recently shown to be related to tumorigenesis, progression and metastasis in different experimental models of malignancy. Malignant pleural mesothelioma (MPM) is a fatal disease in which the prognosis remains very poor and the knowledge of predictive factors for outcome is insufficient. The identification of new molecules involved in cancer initiation and development is a fundamental step for improving the curability of this kind of tumor. The purpose of this study is to define the role of OPN in the diagnosis of MPM by determining its prognostic and diagnostic value., Methods: A group of 24 surgically staged MPM subjects was compared with a group of 31 subjects with nonmalignant pulmonary diseases, and with 37 healthy controls. Tumor tissue was analyzed for OPN by immunohistochemical tests, and plasma OPN levels were measured by an enzyme-linked immunosorbent assay., Results: Plasma OPN levels were not significantly higher in either of the patient groups compared with the control group. Immunohistochemical analysis revealed OPN staining of tumor cells in 21 of 24 MPMs. Receiver operating characteristic curve/area under the curve (ROC/AUC) analysis comparing the plasma OPN levels in the healthy group with those of MPM patients showed 40% sensitivity and 100% specificity at a cutoff value of 60.8 ng of OPN per milliliter (AUC 0.6)., Conclusion: Plasma OPN levels do not discriminate between chronic inflammatory and malignant lung diseases and staining intensity in MPM specimens does not correlate with OPN plasma levels.
- Published
- 2009
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45. The monoclonal anti-BCL10 antibody (clone 331.1) is a sensitive and specific marker of pancreatic acinar cell carcinoma and pancreatic metaplasia.
- Author
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La Rosa S, Franzi F, Marchet S, Finzi G, Clerici M, Vigetti D, Chiaravalli AM, Sessa F, and Capella C
- Subjects
- Adaptor Proteins, Signal Transducing immunology, B-Cell CLL-Lymphoma 10 Protein, Carboxylesterase analysis, Humans, Immunohistochemistry, Metaplasia, Sensitivity and Specificity, Adaptor Proteins, Signal Transducing analysis, Antibodies, Monoclonal immunology, Biomarkers, Tumor analysis, Carcinoma, Acinar Cell diagnosis, Pancreas pathology, Pancreatic Neoplasms diagnosis
- Abstract
Acinar cell carcinoma (ACC) is a rare pancreatic cancer which may be difficult to distinguish from other solid nonadenocarcinoma tumors. The diagnosis depends on the demonstration of acinar differentiation, obtained with antibodies recognizing various pancreatic enzymes that, although specific, show different sensitivity. The C-terminal portion of the BCL10 protein shows homology with carboxyl ester hydrolase (CEH), an enzyme produced by pancreatic acinar cells. We investigated the usefulness of a C-terminal BCL10 monoclonal antibody in the diagnosis of ACCs. We examined normal pancreases and different pancreatic tumors including ACCs, mixed acinar-endocrine carcinomas, ductal adenocarcinomas, mucinous, serous, solid pseudopapillary, and endocrine neoplasms. In addition, various normal tissues and cases of pancreatic metaplasia of the gastroesophageal mucosa, cases of ectopic pancreas, gastrointestinal endocrine tumors, salivary and breast acinic cell carcinomas, gastric adenocarcinomas with and without acinar differentiation, and hepatocellular carcinomas were studied. BCL10 immunoreactivity paralleled that of CEH and was restricted to acinar cells of normal and ectopic pancreas, of pancreatic metaplasia, and of ACCs. The anti-BCL10 antibody was more sensitive in detecting ACCs and pancreatic metaplasia than antibodies directed against other pancreatic enzymes. We suggest using BCL10 antibody for diagnosing pancreatic tumors and whenever an acinar differentiation is suspected in gastrointestinal neoplastic and metaplastic lesions.
- Published
- 2009
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46. Different intracellular compartmentalization of TA and DeltaNp73 in non-small cell lung cancer.
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Di Vinci A, Sessa F, Casciano I, Banelli B, Franzi F, Brigati C, Allemanni G, Russo P, Dominioni L, and Romani M
- Subjects
- Apoptosis, Carcinoma, Non-Small-Cell Lung genetics, Carcinoma, Non-Small-Cell Lung pathology, Cell Line, Tumor, DNA Methylation, DNA Primers, DNA, Neoplasm genetics, Gene Expression Regulation, Neoplastic, Humans, Lung Neoplasms genetics, Lung Neoplasms pathology, Neoplasm Proteins metabolism, Promoter Regions, Genetic, Reverse Transcriptase Polymerase Chain Reaction, Transcription, Genetic, Tumor Protein p73, Carcinoma, Non-Small-Cell Lung metabolism, DNA-Binding Proteins genetics, DNA-Binding Proteins metabolism, Lung Neoplasms metabolism, Nuclear Proteins genetics, Nuclear Proteins metabolism, Tumor Suppressor Proteins genetics, Tumor Suppressor Proteins metabolism
- Abstract
The p53 homologue p73 is overexpressed in many tumors, including lung cancer. We have evaluated the differential expression and subcellular localization of the functionally distinct apoptotic (TA) and anti-apoptotic (DeltaN) isoforms of p73 in non-small cell lung cancer (NSCLC), their possible association with p53 expression and determined the methylation status of the two p73 gene promoters (P1 and P2) in this tumor type. Immunohistochemical analysis showed that both isoforms are expressed in the majority of cases. However, the oncogenic DeltaN variant, derived from the transcripts DeltaN'p73 (from P1) and/or DeltaNp73 (from P2), is localized mainly in the nucleus, while the anti-oncogenic TAp73 isoform (derived from a P1 transcript) is sequestered in the cytoplasm in almost all cases analyzed. Significant correlation was found between p53 and DeltaNp73 expression (p=0.041). Methylation analysis conducted on 41 tumor samples showed that the P1 promoter is almost invariably unmethylated (39/41 cases) whereas P2 was found completely methylated in 17 cases and partially or totally unmethylated in 24 samples. No correlation was found between the methylation status of P1 and P2 and p73 expression. Our results demonstrate that both isoforms contribute to p73 overexpression in NSCLC and suggest that their different intracellular localization may reflect an alteration of the functional p53-p73 network that might contribute to lung cancer development.
- Published
- 2009
47. BACE2 is stored in secretory granules of mouse and rat pancreatic beta cells.
- Author
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Finzi G, Franzi F, Placidi C, Acquati F, Palumbo E, Russo A, Taramelli R, Sessa F, and La Rosa S
- Subjects
- Amyloid Precursor Protein Secretases ultrastructure, Animals, Aspartic Acid Endopeptidases ultrastructure, Immunohistochemistry, Insulin-Secreting Cells ultrastructure, Mice, Microscopy, Electron, Transmission, Rats, Secretory Vesicles ultrastructure, Amyloid Precursor Protein Secretases metabolism, Aspartic Acid Endopeptidases metabolism, Insulin-Secreting Cells enzymology, Secretory Vesicles enzymology
- Abstract
BACE2 is a protease homologous to BACE1 protein, an enzyme involved in the amyloid formation of Alzheimer disease (AD). However, despite the high homology between these two proteins, the biological role of BACE2 is still controversial, even though a few studies have suggested a pathogenetic role in sporadic inclusion-body myositis and hereditary inclusion-body myopathy, which are characterized by vacuolization of muscular fibers with intracellular deposits of proteins similar to those found in the brain of AD patients. Although BACE2 has also been identified in the pancreas, its function remains unknown and its specific localization in different pancreatic cell types has not been definitively ascertained. For these reasons, the authors have investigated the cellular and subcellular localization of BACE2 in normal rodent pancreases. BACE2 immunoreactivity was found in secretory granules of beta cells, co-stored with insulin and IAPP, while it was lacking in the other endocrine and exocrine cell types. The presence of BACE2 in secretory granules of beta cells suggests that it may play a role in diabetes-associated amyloidogenesis.
- Published
- 2008
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48. Physical performance characteristics of assisted living residents and risk for adverse health outcomes.
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Giuliani CA, Gruber-Baldini AL, Park NS, Schrodt LA, Rokoske F, Sloane PD, and Zimmerman S
- Subjects
- Aged, Aged, 80 and over, Female, Hand Strength physiology, Humans, Locomotion physiology, Male, United States, Activities of Daily Living, Assisted Living Facilities, Risk Assessment methods, Task Performance and Analysis
- Abstract
Purpose: Researchers know little about the physical performance ability of residential care/assisted living (RC/AL) residents and its relationship to adverse outcomes such as fracture, nursing home placement, functional decline, and death. The purposes of this article are to (a) describe the functional characteristics of RC/AL residents, (b) examine the relationships between resident- and facility-level characteristics and physical performance, and (c) determine the predictive value of physical performance for adverse outcomes., Design and Methods: Data came from 1,791 residents in 189 RC/AL facilities participating in the Collaborative Studies of Long-Term Care. At baseline, residents were tested on four performance measures (grip strength, chair rise, balance, and walking speed), and other resident- and facility-level information was collected. Adverse outcomes were measured over 1 year., Results: Average grip strength was 14 +/- 7 kg, 61% of residents walked <0.6 m/s (M = 0.41 m/s), 26% could perform five chair rises, and only 19% could perform a tandem stand for a least 1 s. Multivariable analyses showed that more cognitive and functional impairment, depressive symptoms and comorbid conditions, and for-profit ownership were associated with poorer physical performance. Controlling for individual characteristics, we found that better performance on the four physical performance measures was associated with a reduced risk of nursing home placement, fracture, and decline in function over 1 year., Implications: Simple performance measures identify modifiable functional deficits and suggest targeted interventions to prolong independent mobility and aging in place in RC/AL facilities.
- Published
- 2008
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49. Prognostic factors for ampullary adenocarcinomas: tumor stage, tumor histology, tumor location, immunohistochemistry and microsatellite instability.
- Author
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Sessa F, Furlan D, Zampatti C, Carnevali I, Franzi F, and Capella C
- Subjects
- Adenocarcinoma genetics, Adenocarcinoma mortality, Adult, Aged, Aged, 80 and over, CDX2 Transcription Factor, Common Bile Duct Neoplasms genetics, Common Bile Duct Neoplasms mortality, Female, Homeodomain Proteins analysis, Humans, Immunohistochemistry, Male, Middle Aged, Mucins analysis, Neoplasm Staging, Prognosis, Survival Rate, Adenocarcinoma pathology, Ampulla of Vater, Common Bile Duct Neoplasms pathology, Microsatellite Instability
- Abstract
Prognostic factors for ampullary carcinomas (ACs) are poorly defined. Fifty three resected ACs were analyzed for CDX2, MUC1, MUC5AC, MUC6, MUC2, and for mismatch repair proteins (hMLH1, hMSH2, PMS2, hMSH6) using immunohistochemistry. Microsatellite instability (MSI) status was evaluated by fluorescently labeled PCR using an automated sequencer. Univariate and multivariate analysis was performed for clinicopathological, immunohistochemical and molecular parameters. CDX2 was found in 32 out of 53 (60%) ACs with a significantly higher frequency among intestinal ACs compared with biliopancreatic (BP) ACs. The MUC1, MUC5AC, MUC6, MUC2 apomucins were expressed in 75, 43, 39, and 28% of ACs, respectively, with a significantly higher coexpression of MUC1/MUC5AC in BP ACs. MSI and loss of expression of hMLH1/PMS2 or hMSH2/hMSH6 proteins were observed only in intestinal ACs. Factors significantly correlated with improved survival in the univariate analysis were: low stage, absence of lymph nodes metastases, negative surgical margins (R0 status), and presence of MSI. In the multivariate analysis, stage was the only independent prognostic factor of survival. We conclude that stage is the only independent prognostic factor of survival in the multivariate analysis, whereas histological criteria and the immunohistochemical expression of apomucins and CDX2 are helpful in the classification and understanding of the histogenesis of ACs.
- Published
- 2007
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50. Ultrastructural evidence of Tropheryma whippelii in PAS-negative granulomatous lymph nodes.
- Author
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Finzi G, Franzi F, Sessa F, Mastaglio C, and Capella C
- Subjects
- Actinobacteria ultrastructure, Anti-Infective Agents therapeutic use, Granuloma microbiology, Hepatomegaly microbiology, Hepatomegaly pathology, Humans, Lymph Nodes ultrastructure, Lymphatic Diseases microbiology, Lymphatic Diseases pathology, Macrophages microbiology, Macrophages ultrastructure, Male, Mesentery pathology, Middle Aged, Periodic Acid-Schiff Reaction, Splenomegaly microbiology, Splenomegaly pathology, Treatment Outcome, Trimethoprim, Sulfamethoxazole Drug Combination therapeutic use, Whipple Disease drug therapy, Whipple Disease microbiology, Actinobacteria isolation & purification, Granuloma pathology, Lymph Nodes microbiology, Whipple Disease pathology
- Abstract
The presence of Tropheryma whippelii was demonstrated in the PAS-negative mesenteric granulomatous lymph nodes of a patient affected by Whipple disease. Ultrastructurally a few bacteria, enclosed by a membrane characteristic of Tropheryma whippelii, were found in the extracellular spaces and remnants of bacteria were found in the phagocytic vacuoles of macrophages. The scarce number of bacilli, probably due to the fact that the disease was at an initial phase, could explain the absence of PAS positivity. This case confirms the role of the electron microscopy in the diagnosis of Whipple disease, especially for extra-intestinal lesions and at the initial phase of the disease, when the characteristic PAS-positive macrophages can be absent.
- Published
- 2007
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