233 results on '"E, Comperat"'
Search Results
2. Impact pronostique de l’expression de pd-1 et pd-l1 pour les tumeurs de la voie excrétrice supérieure
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L. Campedel, J. Varinot, G. Cancel-tassin, M. Rouprêt, P. Gabriel, G. Daniel, M. Decaussin-petrucci, C. Eymerit, C. Lebacle, S. Ferlicot, F. Mège-lechevalier, V. Lindner, P. Léon, A. Durlach, F. Gobet, N. Vuong, M. Philip, O. Cussenot, E. Comperat, and T. Seisen
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Urology - Published
- 2022
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3. Genomic profiling of urothelial carcinoma in situ of bladder
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M. Anurag, T. Strandgaard, S. Kim, E. Comperat, H. Al-Ahmadie, B.A. Inman, L. Dyrskjot, and S. Lerner
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Urology - Published
- 2023
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4. En-bloc vs. conventional resection of primary bladder tumor (eBLOC): A multicenter, open-label, phase 3 randomised controlled trial
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D. D’Andrea, F. Soria, R. Hurle, D. Enikeev, S. Kotov, E. Xylinas, L. Lusuardi, A. Heidenreich, D. Gu, N. Frego, M. Taraktin, M. Ryabov, P. Gontero, E. Comperat, and S.F. Shariat
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Urology - Published
- 2022
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5. En-bloc vs conventional resection of primary bladder tumor (EBLOC): a multicenter, open-label, phase 3 randomised controlled trial
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F. Soria, D. D’andrea, R. Hurle, D. Enikeev, S. Kotov, A. Heidenreich, L. Lusuardi, N. Frego, M. Ryabov, P. Gontero, E. Comperat, and S. Shariat
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Urology - Published
- 2022
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6. Assessing the impact of BCG on progression of NMIBC in the new EAU high risk and very high-risk groups
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P. Gontero, J.L. Dominguez-Escrig, B.W.G. Van Rhijn, A.H. Mostafid, M. Roupret, D. Cohen, E. Comperat, F. Liedberg, J. Palou Redorta, M. Burger, S. Shariat, T. Seisen, V. Soukup, A. Masson-Lecomte, O. Capoun, M. Babjuk, and R.J. Sylvester
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Urology - Published
- 2022
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7. Assessment of systematic and combined MRI-targeted biopsy for prostate cancer diagnosis during 10 years of practice at a single institution
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L. Lenfant, R. Renard-Penna, Y. De Rycke, M. Roupret, A. Baugerie, E. Comperat, E. Chartier-Kastler, and P-C. Mozer
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Urology - Published
- 2022
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8. RE-TUR + BCG vs. upfront BCG in high-risk non-muscle invasive bladder cancer: A feasibility phase of a randomized controlled study
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F. Soria, M. Rosazza, M. Burger, E. Comperat, F. Liedberg, A. Masson-Lecomte, H. Mostafid, B.W. Van Rhijn, S.F. Shariat, M. Babjuk, R.J. Sylvester, J. Palou, and P. Gontero
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Urology - Published
- 2022
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9. Surveillance des carcinomes urothéliaux : revue du Comité de cancérologie de l’Association française d’urologie
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Nadine Houede, Géraldine Pignot, Catherine Roy, H. Quintens, Y. Neuzillet, membres du Comité de cancérologie de l’Association française d’urologie, Christian Pfister, Michel Soulié, Morgan Rouprêt, E. Comperat, Stéphane Larré, and Pierre Colin
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Gynecology ,03 medical and health sciences ,medicine.medical_specialty ,0302 clinical medicine ,business.industry ,030220 oncology & carcinogenesis ,Urology ,030232 urology & nephrology ,Medicine ,business ,3. Good health ,Urothelial carcinoma - Abstract
Resume Introduction Le Comite de cancerologie de l’Association francaise d’urologie (CCAFU) a realise une revue de la litterature concernant la surveillance des carcinomes urotheliaux et propose des recommandations de suivi. Materiel et methode Une recherche bibliographique en langue francaise et anglaise a partir de PubMed » a ete effectuee de 1990 a 2014 en utilisant les mots cles « carcinome urothelial », « suivi », « pronostic », et « recidive ». Resultats Le rythme et les moyens de surveillance (cytologie, fibroscopie, uro-TDM) des tumeurs de la vessie non infiltrant le muscle (TVNIM) doivent etre adaptes aux risques de recidive et de progression definis selon les tables de l’EORTC. Apres traitement radical d’une tumeur de la vessie infiltrant le muscle (TVIM), la surveillance est basee sur la fibroscopie, la cytologie et la realisation d’une imagerie de coupe avec temps tardifs. La surveillance de l’uretre doit etre adaptee aux facteurs de recidive et poursuivie au moins 5 ans. La surveillance du haut appareil est a poursuivre a vie. En cas de traitement conservateur d’une TVIM, une reevaluation precoce par imagerie et fibroscopie est necessaire. Apres traitement radical d’une tumeur des voies excretrices superieures (TVES), la surveillance par cystoscopie et cytologie est essentielle en raison de la frequence des recidives vesicales au cours des trois premieres annees. Le traitement conservateur des TVES necessite une surveillance stricte notamment par uretero-renoscopie. Conclusion La surveillance des carcinomes urotheliaux est a adapter en fonction des stades et grades tumoraux, de la localisation et de la modalite de traitement definissant ainsi le risque de recidive dans le temps.
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- 2015
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10. [Prognostic value of PD-1/PD-L1 expression in upper tract urothelial carcinoma]
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L, Campedel, T, Seisen, O, Cussenot, E, Comperat, J, Varinot, M, Rouprêt, and G, Cancel-Tassin
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Carcinoma, Transitional Cell ,Urologic Neoplasms ,Predictive Value of Tests ,Programmed Cell Death 1 Receptor ,Biomarkers, Tumor ,Humans ,Prognosis ,Immunohistochemistry ,B7-H1 Antigen - Abstract
Current literature supports the efficacy of anti-PD-1 and anti-PD-L1 immune checkpoint inhibitors for the treatment of urothelial carcinomas. While the prognostic value of PD-1 and PD-L1 levels has been comprehensively analyzed for urothelial carcinoma of the bladder, less is known for upper tract urothelial carcinoma. In addition, available data on the prognostic value of PD-1 and/or PD-L1 level in the tumor and/or peritumoral microenvironment are heterogeneous and even sometimes contradictory. In this article, we compared the methodologies of the various available studies in order to highlight the factors that can explain these discordant results.
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- 2018
11. [Sporadic kidney cancer of young subjects: Study of the clinical and pathological features of a bicentric cohort]
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J, Cohen, M O, Timsit, O D, Zerbib, M, Rouprêt, V, Verkarre, E, Comperat, A, Mejean, and M O, Bitker
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Adult ,Male ,Young Adult ,Adolescent ,Incidence ,Age Factors ,Humans ,Female ,Kidney Neoplasms ,Retrospective Studies - Abstract
The epidemiology of kidney cancer is evolving with a net increase in the incidence of renal tumors, globally, and in young people in particular.To evaluate the incidence and clinical and pathological characteristics of sporadic renal tumors in young subjects and their risk factors.A retrospective study aimed at collecting clinical, epidemiological and anatomopathological information from the 118 patients aged 18 to 40 treated for a sporadic kidney tumor in two Parisian university hospital centers between 2003 and 2013.Our study showed a very significant increase in the incidence of renal tumors in our 11 years of decline (P=6.10Our study showed a marked increase in the incidence of renal tumors with specific clinical and epidemiological features in a population of young subjects. The role and importance of oncogenetic management as well as the study of environmental factors could lead to the identification of new risk factors and corollary to their prevention.4.
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- 2017
12. Prognostic performance and reproducibility of the 1973 and 2004/2016 WHO grading classification systems in non-muscle-invasive bladder cancer: A European Association of Urology non-muscle invasive bladder cancer guidelines panel systematic review
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V. Soukup, O. Čapoun, D. Cohen, V. Hernandez, M. Babjuk, M. Burger, E. Comperat, P. Gontero, T. Lam, S. MacLennan, A.H. Mostafid, J. Palou, B.W.G. Van Rhijn, M. Roupret, S.F. Shariat, R. Sylvester, Y. Yuan, and R. Zigeuner
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Urology - Published
- 2018
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13. Tumeurs de vessie intradiverticulaires : revue du Comité de cancérologie de l’Association française d’urologie
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Yann Neuzillet, Christian Pfister, Morgan Rouprêt, H. Quintens, H. Wallerand, E. Comperat, Catherine Roy, Géraldine Pignot, Michel Soulié, Nadine Houede, and Stéphane Larré
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Gynecology ,medicine.medical_specialty ,business.industry ,Urology ,medicine ,Bladder tumor ,Neoplasm staging ,business ,Urothelial carcinoma - Abstract
Resume Introduction Le Comite de cancerologie de l’Association francaise d’urologie (CCAFU) a realise une revue de la litterature sur l’epidemiologie, le diagnostic et les traitements des tumeurs de vessie intradiverticulaires (TVID) et a propose des propositions therapeutiques. Materiel et methode Une recherche bibliographique en langue francaise et anglaise par Medline ® en utilisant les mots cles « tumeurs », « vessie » et « diverticule » a ete effectuee. Resultats Les TVID etaient plus frequemment de stade T ≥ 3a et de types histologiques non urotheliaux que les tumeurs de vessie classiques. Lors de leur diagnostic, un risque de sous-evaluation de l’extension et de la multifocalite tumorale a ete constate. Leur pronostic a ete plus pejoratif que celui des tumeurs classiques qui incite a une limitation de l’indication des traitements conservateurs. Les niveaux de preuves de publications analysees etaient faibles, avec un niveau C selon le score de Sackett. Conclusion Les specificites des TVID a conduit le CCAFU a proposer des prise en charge therapeutiques specifiques, se basant sur de faible niveaux de preuves. Les TVID Ta-T1 et de bas grade peuvent etre traitees par une resection endoscopique seule ou suivi d’une BCG therapie en cas de carcinome in situ associe. Les TVID de haut grade, unique et sans carcinome in situ associe, peuvent etre traitees par diverticulectomie associee a un curage ganglionnaire pelvien. Les TVID de haut grade, multiples ou associees a du carcinome in situ, justifient une cystectomie totale.
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- 2012
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14. [Pathological advances in renal, prostatic, bladder and testis neoplasia]
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N, Rioux-Leclercq, E, Comperat, S-F, Kammerer-Jacquet, P, Camparo, and G, Fromont
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Male ,Testicular Neoplasms ,Urinary Bladder Neoplasms ,Humans ,Prostatic Neoplasms ,Kidney Neoplasms - Abstract
The ISUP (International Society of Urological Pathology) Consensus Conferences between 2012 and 2015 made recommendations regarding the classification, staging, prognostic factors of adult tumors from kidney, prostate, bladder and testis. The main points of these recommendations are highlighted in this article.This article is based on a systematic literature search by using different keywords "cancer, kidney, prostate, bladder, testis, pathology, classification" from Pubmed database. Only publications between 2012 and 2015 were retained.The different Consensus conferences since 2012 in uropathology have provided international guidelines for the classification, grading and staging of tumors in kidney, bladder, prostate and testis. We identified in this article the main points of these new guidelines that are about to be published in the new 2016 WHO classification of urogenital tract tumors in adult.New pathological guidelines in urogenital tumors have to be taken into account for a better diagnosis and therapy.
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- 2016
15. [Not Available]
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B, Peyronnet, S, Kozal, T, Seisen, E, Comperat, C, Vaessen, P, Mozer, R, Renard-Penna, M, Bitker, E, Chartier-Kastler, O, Cussenot, M, Rouprêt, and S, Drouin
- Published
- 2015
16. [Not Available]
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L, Salomon, S, Bastuji-Garin, C, Mazerolles, M, Devonec, M, Soulie, G, Benoit, P, Rischmann, M, Decaussin-Petrucci, N, Mottet, D, Gasman, G, Fromont-Hankard, J, Irani, A, De la Taille, M, Zerbib, S, Ferlicot, E, Comperat, C, Vaesen, F, Beuvon, T, Lebret, E, Boutin, F, Mege-Lechevallier, B, Dore, C, Radulescu, M, Paoletti, A, Shar, M, Colombel, and E, Lechevallier
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- 2015
17. [Not Available]
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R, Renard-Penna, G Cancel, Tassin, E, Comperat, P, Leon, M, Roupret, P, Mozer, M, Bitker, and O, Cussenot
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- 2015
18. [Not Available]
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A, Mason-Lecomte, E, Xylinas, P, Colin, E, Comperat, F, Dubosq, N, Houedee, S, Larré, Y, Neuzillet, G, Pignot, P, Puech, A, Mejean, B, Qvick, P, Bes, and M, Rouprêt
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- 2015
19. [Not Available]
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V, Phe, M, Rouprêt, O, Cussenot, E Chartier, Kastler, X, Game, and E, Comperat
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- 2015
20. [Observational survey of the French Urological Association Oncology Committee (CCAFU) evaluating the practice of immediate postoperative instillation (IPOP) using mitomycin C for non-muscle invasive bladder cancer (NMIBC) treatment]
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Y, Neuzillet, P, Colin, E, Comperat, F, Dubosq, N, Houede, S, Larre, A, Masson-Lecomte, G, Pignot, P, Puech, M, Roumiguie, E, Xylinas, A, Mejean, and M, Roupret
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Postoperative Care ,Administration, Intravesical ,Time Factors ,Urinary Bladder Neoplasms ,Health Care Surveys ,Mitomycin ,Urology ,Humans ,Neoplasm Invasiveness ,France ,Practice Patterns, Physicians' ,Combined Modality Therapy ,Societies, Medical - Abstract
To evaluate the practice of immediate postoperative instillation (IPOP) using mitomycin C for non-muscle invasive bladder cancer (NMIBC) treatment by urologists members of the French Association of Urology (AFU).Internet-based observational survey evaluating indications and practical modalities of IPOP in NMIBC treatment using questionnaire sent in May 2014 to 915 urologists.Two hundred ninety-eight urologists participated in the survey (response rate: 32.6%) and 57% prescribed the IPOP. The median frequency of IPOP prescription was 3.3%, and was higher in the academic public sector. The CASE recommendations were self-assessed as known or well-known in 67% of cases. The selections criteria for IPOP were adequately identified by 62% of urologists, without differences according to sectors of activity. The IPOP prescription modalities were declared as an obstacle to the completion for 41.9% of urologists, and especially in the private sector. Completion times of IPOP were declared24h in 91% of cases. We see that 28.5% of urologists prescribed an urinary alkalization. The average frequency of complications of IPOP was 0.91 per urologist.The IPOP prescription frequency was higher among urologists practicing in the academic sector. Neither the level of knowledge of the recommendations nor the frequency of complications of IPOP had explained this difference. However, the prescription modalities were more frequently reported as an obstacle to their completion in the private sector.3.
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- 2015
21. [Pathologic analysis of upper tract urothelial carcinomas: state of the art review for the yearly scientific report of the French National Association of Urology]
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J, Varinot, P, Colin, M, Rouprêt, X, Leroy, and E, Comperat
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Carcinoma, Transitional Cell ,Urologic Neoplasms ,Biopsy ,Adenocarcinoma ,Prognosis ,Immunohistochemistry ,Carcinoma, Papillary ,Carcinoma, Neuroendocrine ,Lymphatic Metastasis ,Carcinoma, Squamous Cell ,Humans ,Microsatellite Instability ,Neoplasm Invasiveness ,Neoplasm Grading ,Urothelium ,Neoplasm Staging - Abstract
Upper tract urothelial carcinomas (UTUC) are rare tumors. Pathologist have a crucial role in establishing the diagnosis and the evaluation of the prognosis of these tumors.A systematic review of the scientific literature was performed in the Medline database (PubMed) using different associations of the following key words alone or concomittantly: ureter; renal pelvis; urothelial carcinoma; specimen; pathology; histology; classification; grade; stage; prognosis. A particular search was done on the characteristics of the specimen management provided by urologists to pathologists and main prognostic specificities expected in UTUCs.Urinary cytology and biopsies are useful to provide the grade of the tumor according to the WHO classification 2004. The urologist needs to depict the clinical context to the pathologist in order to eliminate differential diagnosis. The main prognostic informations provided by the pathologist from the specimen analysis are the following: stage (TNM 2009), grade (WHO 2004), carcinoma in situ, location within upper tract, multifocality, necrosis, tumor size, lymphovascular invasion, margins and potentially microsatellite status when a HNPCC case is suspected.The pathologic analysis of a UTUC specimen needs nowadays to fulfill standardised international criteria of quality. However, specific additional aspects reported in the literature (e.g., lymphovascular invasion) are not systematically depicted.
- Published
- 2014
22. [Surgical treatment of metastatic urothelial carcinoma of the bladder: Review of the Cancer Committee of the French Association of Urology]
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Y, Neuzillet, S, Larré, E, Comperat, M, Rouprêt, G, Pignot, N, Houede, H, Quintens, H, Wallerand, C, Roy, M, Soulie, and C, Pfister
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Carcinoma, Transitional Cell ,Urinary Bladder Neoplasms ,Humans ,Cystectomy - Abstract
The role of surgery in the treatment of patients with metastatic urothelial bladder cancer is controversial. The aim was to review situations where surgical resection of the bladder tumor and/or metastatic urothelial carcinoma has been reported and analyze its results.A bibliographic research in French and English using the keywords BCG, bladder cancer, metastases, cystectomy, metastasectomy, radiotherapy, curative treatment and palliative treatment was performed, 177 articles have been reviewed, and 18 have been selected.Synchronous or metachronous urothelial carcinoma metastases were diagnosed in 4 and 50% of the cases, respectively. The surgical treatment of metastatic urothelial carcinoma of the bladder has been proposed to achieve oncologic resection of all detectable lesions after a first-line chemotherapy or to treat symptoms, which were refractory to other treatment modalities. In achieving complete resection of the primary tumor and metastases after MVAC chemotherapies, the 5years overall survival was 28%.There was no evidence in favouring surgical treatment of metastatic urothelial carcinoma. Considering the high perioperative mortality rate of cystectomy in imperative indications, particularly in the case of hematuria, all therapeutic alternatives must have been exhausted and urine derived in the simplest way.
- Published
- 2013
23. [Prognostic influence of prostate gland invasion by bladder tumour and/or prostate cancer in cystoprostatectomy specimen: a review]
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C M, Champy, V, Phé, S J, Drouin, E, Comperat, J, Parra, C, Vaessen, P, Mozer, M-O, Bitker, and M, Rouprêt
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Male ,Prostatectomy ,Survival Rate ,Incidental Findings ,Urinary Bladder Neoplasms ,Incidence ,Humans ,Prostatic Neoplasms ,Neoplasm Invasiveness ,Cystectomy ,Prognosis ,Neoplasm Staging - Abstract
Cystoprostatectomy (CPT) is the gold standard surgical treatment for muscle invasive bladder cancer (MIBC). In certain cases, MIBC can invade the prostate gland and/or a prostate cancer (PCa) can be discovered fortuitously on the pathologic specimen. The aim of the current study was to report the prognostic influence of PCa in patients who underwent a CPT for MIBC.A systematic review of the scientific literature was achieved in the Pubmed database, using the following keywords: prostatic neoplasm; urinary bladder neoplasm; cystectomy; surgery; recurrence; prognosis; survival. Clinical cases and series of less than five cases were deliberately excluded herein.Overall, ten studies published between 2004 and 2011 and involving 2196 patients were selected. Only retrospective studies of low level of evidence (NP 4) were available. The incidence of neoplastic invasion of the prostate gland by MIBC ranged from 25 to 48%. Preoperative predictors were multiple BC, recurrent, location in the trigone and existence of CIS. Overall survival at 3 years was significantly affected by the invasion of the prostate gland (pT4a) in these patients. The incidence of PCa discovered incidentally pathologic specimen CPT ranged from 14 to 49%. Only age was found as a positive predictor. The diagnosis of PCa did not influence survival of patients with MIBC and no specific PCa adjuvant treatment was systematically advocated.Fortuitous diagnosis of PCa and/or neoplastic invasion of the prostatic gland by BC on CPT specimen is not uncommon but this is variable across studies, depending on the quality of the pathological analysis. The invasion of the prostate gland by MIBC is a serious situation (pT4a) and linked with a poor prognosis. In case of concomitant PCa and MIBC, the prognosis is much more related to the natural history of the bladder tumour.
- Published
- 2012
24. [Intradiverticular bladder tumours: review of the Cancer Committee of the French Association of Urology]
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Y, Neuzillet, E, Comperat, M, Rouprêt, S, Larre, C, Roy, H, Quintens, N, Houede, G, Pignot, H, Wallerand, M, Soulie, and C, Pfister
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Diagnostic Imaging ,Diverticulum ,Urinary Bladder Neoplasms ,Urinary Bladder ,BCG Vaccine ,Humans ,Cystectomy ,Combined Modality Therapy ,Neoplasm Staging - Abstract
Cancer Committee of the French Association of Urology (CCAFU) conducted a review of the epidemiology, diagnosis and treatment of intradiverticular bladder tumours (TVID) and proposed therapeutic management.A bibliographic research in French and English using Medline(®) with the keywords "tumor", "bladder" and "diverticulum" was performed.TVID are more frequently of stage T ≥ 3a and with non urothelial histology than classical bladder tumors. At diagnosis, the risk of underestimation of the extent and multifocality of the tumor was described. Their prognosis, that was more pejorative than conventional tumors, should impelled to limit the indications of conservative treatment. The evidence levels of analyzed publications were low, with C level according to Sackett score.the specificities of the TVID have lead the CCAFU to propose specific therapeutic guidelines, based on poor evidence level. Ta-T1 low grade TVID can be treated by transurethral resection alone or followed by BCG therapy in cases of associated carcinoma in situ. High-grade TVID, unifocal and without associated carcinoma in situ, can be treated by diverticulectomy associated with pelvic lymphadenectomy. High grade TVID, multiple or associated with carcinoma in situ, warranted total cystectomy.
- Published
- 2012
25. [Primary upper urinary tract tumors and subsequent location in the bladder]
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M-D, Azémar, M, Audouin, A, Revaux, V, Misraï, E, Comperat, M-O, Bitker, E, Chartier-Kastler, F, Richard, O, Cussenot, and M, Rouprêt
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Carcinoma, Transitional Cell ,Urinary Bladder Neoplasms ,Risk Factors ,Ureteral Neoplasms ,Humans ,Neoplasms, Second Primary ,Kidney Neoplasms - Abstract
The urothelium is the epithelium that lines the upper and lower urinary tract. Over 95% of urothelial carcinomas are derived from urothelium. They can be located in the lower tract (bladder, urethra) or upper tract (pyelocaliceal cavities, ureter). Urothelial carcinomas are the fourth most common tumours after prostate (or breast) cancer, lung cancer and colorectal cancer. On one hand, bladder tumours account for 90-95% of urothelial carcinomas. It is the most common malignancy of the urinary tract and the second most common malignancy of the urogenital tract after prostate cancer. It accounts for 5-10% of all cancers diagnosed each year in Europe. On the other hand, upper urinary tract urothelial cell carcinomas (UUT-UCC) are scarce and account for only 5-10% of urothelial carcinomas. Recurrence in the bladder after primary UUT-UCC occurs in 15-50% of UUT-UCC. Differences in treatment modalities of the primary UUT-UCC do not play a key role in the subsequent appearance of a bladder recurrence. However, others factors have been described such as stage and location in the upper tract of the primary tumour or upper tract tumour multifocality. Previous history of bladder tumour is also associated with the risk that another tumour arises in the bladder subsequently. However, it becomes difficult to distinguish between natural history of bladder tumour and evolution of UUT-UCC in these cases. In most cases, bladder cancer occurs in the first two years after UUT-UCC management. Surveillance protocol is based on cystoscopy and on urinary cytology during at least every three months for two years. Current surveillance regimen have a low level of evidence considering the paucity of UUT-UCC.
- Published
- 2009
26. [Results of nephron-sparing surgery for renal cell carcinoma of more than 4 cm in diameter]
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M, Peycelon, C, Vaessen, V, Misraï, E, Comperat, P, Conort, M-O, Bitker, A, Haertig, E, Chartier-Kastler, F, Richard, and M, Rouprêt
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Humans ,Nephrons ,Carcinoma, Renal Cell ,Nephrectomy ,Kidney Neoplasms - Abstract
To date, radical nephrectomy (RN) remains the gold standard treatment for renal cell carcinoma (RCC) larger than 4 cm. However, from the early 1990's, improvements in surgical techniques have lead to the development of nephron-sparing surgery (NSS) for small renal tumours of less than 4 cm in diameter. This surgical procedure avoids nephronic waste with an acceptable morbidity and similar oncological outcomes compared to radical surgery. Recent large published series did not show any difference between NSS and RN in terms of oncological safety. Specific and disease-free five-year survival rates (82% to 97.3% and 81% to 97.3%, respectively) have confirmed the safety of NSS. Regarding laparoscopic NSS, the technique is still under evaluation and only mid-term outcomes are available so far. However, these studies are still limited and longer follow-up is needed before any definitive statement can be made. Current guidelines recommend NSS only in case of RCC of less than 4 cm in diameter in elective indications. In daily practice however, surgical teams are pushing back the limit above the threshold of 4 cm. More and more surgeons are either considering anatomical location or technical expected difficulties rather than just the tumour size. NSS leads to higher risk of bleeding, especially in case of tumours larger than 4 cm. Therefore, it is absolutely necessary to investigate thoroughly the vascularization of the tumour to avoid such complications with exhaustive and accurate preoperative imaging.
- Published
- 2008
27. [Ductal adenocarcinoma, four years follow-up]
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A, Dohan, S, Bart, R, Renard-Penna, E, Comperat, F, Thibault, A, Doerfler, and F, Richard
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Male ,Time Factors ,Humans ,Prostatic Neoplasms ,Adenocarcinoma ,Aged ,Follow-Up Studies - Abstract
Ductal adenocarcinoma of the prostate (DAP) is an unusual form of prostatic cancer rising in the light of the acini and prostatic ducts with preservation of their architecture. We report the case of a 78-year-old patient presenting a pure ductal adenocarcinoma of the prostate locally advanced, with a four years' follow-up. With this case, we report the principal aspects of the literature.
- Published
- 2008
28. [Primary carcinoma of the head of the epididymis]
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F, Thibault, S, Bart, O, Rixe, E, Comperat, R, Renard, E, Chartier-Kastler, and F, Richard
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Adult ,Epididymis ,Male ,Carcinoma ,Genital Neoplasms, Male ,Humans - Abstract
The authors report the case of a 44-year-old man in whom a poorly differentiated primary carcinoma of the head of the epididymis was discovered incidentally. Due to the rarity of this diagnosis, a comprehensive assessment was performed looking for a primary tumour, but without success. Despite early surgical resection, the patient developed lymph-node metastases. This exceptional tumour showed low sensitivity to chemotherapy. Malignant tumours of the epididymis are exceptional and require investigations to detect a primary tumour. Treatment is based on surgical resection, ideally via an inguinal incision, combined with chemotherapy adapted to the histological type.
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- 2008
29. [Crohn's disease presenting with colovesical fistula]
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P, Simon, N, Turin, E, Comperat, Y, Benhamou, M-O, Bitker, and F, Richard
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Adult ,Diagnostic Imaging ,Male ,Crohn Disease ,Urinary Bladder Fistula ,Intestinal Fistula ,Humans - Abstract
Crohn's disease is responsible for 20% of uroenteric fistulas and is the first aetiology of colovesical fistula in young patients. The authors report an unusual case of rectovesical fistula and discuss diagnosis and treatment of Crohn's urodigestive fistulas.A young patient, 38 years old, non smoker, was operated of a suspected bladder tumor by a transuretral approach. Postoperatively appeared a pneumaturia, later on related to a rectovesical fistula. Histology was unclear reporting inflammatory pseudotumor of the bladder. A laparotomy was then performed as the patient was in incomplete bowel occlusion. Peroperative findings and pathological analysis were in favor of a Crohn's disease which was confirmed by secondary study of pathology samples. Resection of terminal ileum and cure of rectovesical fistula protected by a colostomy were performed. The patient completely recovered with an adjuvant medical treatment by infliximab (Remicade).The authors discuss diagnosis management of a pneumaturia and the occurrence of various Crohn's disease related urodigestive fistulas. A review of recently published papers emphasises the interest of using monoclonal antibodies in the medical treatment of Crohn's fistulas after discarding abdominal tuberculosis. In every cases anyway, surgery remains indicated when diagnosis work up reveals presence of an abscess or a bowel stenosis.Crohn's disease should be evocated when histology is not relevant in front of a bladder pseudotumor or a rectovesical fistula.
- Published
- 2007
30. [Neoadjuvant therapy for renal cancer]
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F, Thibault, O, Rixe, J-B, Meric, R, Renard-Penna, H, Boostan, P, Mozer, E, Comperat, F, Richard, and M-O, Bitker
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Male ,Indoles ,Antineoplastic Agents ,Nephrectomy ,Kidney Neoplasms ,Neoadjuvant Therapy ,Treatment Outcome ,Chemotherapy, Adjuvant ,Sunitinib ,Humans ,Lymph Node Excision ,Pyrroles ,Tomography, X-Ray Computed ,Carcinoma, Renal Cell ,Aged - Abstract
A 73-year-old man presented with renal cell carcinoma of the left kidney. Despite the absence of metastases, primary nephrectomy was not performed immediately due to the large tumour volume and the presence of large lymph node extension. The patient was treated with sunitinib for 10 months. Computed tomography at the end of treatment showed a significant reduction of the size of the tumour and the volume of lymph node extension. Radical nephrectomy was then performed. On histological evaluation, the primary renal tumour and, to a lesser degree, the lymph nodes were predominantly necrotic.
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- 2007
31. [Bladder cancer and neurogenic bladder]
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A, Ruffion, E, Comperat, M, Roupret, and E, Chartier-Kastler
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Urinary Bladder Neoplasms ,Carcinoma, Squamous Cell ,Humans ,Urinary Bladder, Neurogenic ,Prognosis ,Risk Assessment - Abstract
In 2006, the risk of developing bladder tumour remains an important aspect of the management and surveillance of spinal cord injury patients. Based on a review of the literature, the authors show that these patients present a particularly high risk of squamous cell carcinoma of the bladder Risk factors remain controversial, but the duration of neurogenic bladder and the voiding mode appear to be the main risk factors. The authors discuss the optimal diagnostic modalities in this setting and the particular case of bladder augmentation.
- Published
- 2007
32. [Disorders of bladder compliance and neurogenic bladder]
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E, Chartier-Kastler, E, Comperat, and A, Ruffion
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Administration, Intravesical ,Urinary Bladder Diseases ,Humans ,Renal Insufficiency ,Botulinum Toxins, Type A ,Urinary Bladder, Neurogenic ,Spinal Cord Injuries - Abstract
Bladder compliance is defined as the relationship between change in bladder volume and change in detrusor pressure (DV/DP). The pathophysiology of neurogenic disorders of bladder compliance is still poorly understood. Experimental reduction of blood flow in the bladder wall, bilateral hypogastric nerve section in rats, the study of spinalized rat bladders, and reduction of oestrogen impregnation show that these conditions induce loss of the viscoelastic properties of the bladder. With the arrival of new treatments active on afferent and/or efferent pathways or on the central nervous system, it is very important to improve our understanding of the pathophysiology of neurogenic disorders of bladder compliance. The reversibility of these disorders constitutes a major therapeutic challenge and their functional consequences constitute a crucial prognostic element of neurogenic bladder. Disorders of bladder compliance can be assessed clinically from two points of view: 1) The natural history of onset of these disorders in neurogenic bladder. Clinical experience demonstrates certain risk factors for the development of these disorders, such as the voiding mode (intermittent self-catheterization or by a carer versus indwelling catheter), the level of the spinal cord lesion (suprasacral versus sacral, incomplete versus complete, and cauda equina lesions), and the presence of myelomeningocele. 2) Data derived from conservative management of these disorders in patients with neurogenic bladder: urethral dilatation, various types of sphincterotomy, vesical denervation, alpha-blockers, sympatholytics, vanilloids (resiniferatoxin and capsaicin), intra-detrusor botulinum toxin and intrathecal baclofen have been shown to improve disorders of compliance of neurogenic bladder.
- Published
- 2007
33. Metastin (KISS-1) and metastin-coupled receptor (GPR54) expression in transitional cell carcinoma of the bladder
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G Cancel-Tassin, Nathalie Nicolaiew, E Comperat, G Nicolle, and Olivier Cussenot
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Regulation of gene expression ,Carcinoma, Transitional Cell ,Kisspeptins ,business.industry ,Tumor Suppressor Proteins ,Hematology ,medicine.disease ,KISS (TNC) ,Receptors, G-Protein-Coupled ,Gene Expression Regulation, Neoplastic ,Transitional cell carcinoma ,Cell Transformation, Neoplastic ,Oncology ,Urinary Bladder Neoplasms ,Kisspeptin-1 ,Cell Line, Tumor ,medicine ,Carcinoma ,Cancer research ,Humans ,RNA, Messenger ,Receptor ,business ,Receptors, Kisspeptin-1 - Published
- 2006
34. 283 Incidence and prognostic impact of prostate cancer on cystectomy specimens: results of a French multicenter study
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G. Pignot, L. Salomon, Y. Neuzillet, A. Masson-Lecomte, C. Lebacle, J-J. Patard, P. Lunardi, P. Rischmann, G. Pasticier, J-C. Bernhard, J. Cohen, M-O. Timsit, B. Peyronnet, G. Verhoest, C. Legoux, M. Zerbib, F. Brecheteau, P. Bigot, S. Larre, T. Murez, R. Thuret, E. Lacarriere, C. Champy, M. Rouprêt, E. Comperat, J. Berger, A. Descazeaud, S. Lavilledieu, C. Avances, F. Delage, A. Valeri, B. Molimard, X. Durand, A. Houlgatte, P. Gres, A. Donnaint, F. Kleinclauss, S. Legal, A. Doerfler, N. Koutlidis, L. Cormier, J-F. Hetet, P. Colls, A. Arvin-Berod, J-J. Rambeaud, H. Quintens, M. Soulie, and C. Pfister
- Subjects
Cystectomy ,Oncology ,Prostate cancer ,medicine.medical_specialty ,Multicenter study ,business.industry ,Urology ,medicine.medical_treatment ,Incidence (epidemiology) ,Internal medicine ,medicine ,medicine.disease ,business - Published
- 2013
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35. Expression et fonction de deux corégulateurs du récepteur des androgènes, SRC2 et HBO1, dans le testicule humain
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P. Camparo, V. Izard, E. Comperat, S. Viengchareun, Lavinia Vija, Jacques Young, G. Meduri, Marc Lombès, and Viorel Vasiliu
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Endocrinology ,Endocrinology, Diabetes and Metabolism ,General Medicine - Published
- 2012
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36. 694 CROSS-CULTURAL VALIDATION OF A PROGNOSTIC TOOL: EXAMPLE OF THE LIMITATIONS OF THE KATTAN PREOPERATIVE NOMOGRAM AS A PREDICTOR OF PROSTATE CANCER RECURRENCE AFTER RADICAL PROSTATECTOMY
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M. Rouprêt, V. Hupertan, E. Comperat, S.J. Drouin, V. Phé, E. Xylinas, M. Sibony, M.O.B. Bitker, E. Chartier-Kastler, F. Richard, and O. Cussenot
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Urology - Published
- 2009
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37. L’imagerie ultrasonore morphologique et fonctionnelle chez la souris
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E. Comperat, Y. Badachi, Michele Lamuraglia, Sébastien Mulé, O. Rixe, Olivier Lucidarme, A. Guibal, E. Jouannot, L. Taillade, and Lori Bridal
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Radiological and Ultrasound Technology ,Radiology, Nuclear Medicine and imaging - Abstract
Objectifs Connaitre l’apport de l’echographie haute frequence dans un essai therapeutique tumoral. Connaitre la technique d’imagerie fonctionnelle de contraste. Reconnaitre en ultrasonographie de contraste les modifications fonctionnelles associees a l’angiogenese. Points cles Les mesures fonctionnelles peuvent permettre une detection plus precoce de la reponse anti-angiogenique que les mesures morphologiques conventionnelles. Ces techniques peuvent contribuer a la comparaison des associations therapeutiques et a l’acceleration des essais pre-cliniques. L’application clinique de l’imagerie ultrasonore fonctionnelle pourrait contribuer a une meilleure optimisation therapeutique en tenant compte de la reponse individuelle du patient. Resume L’echographie haute-resolution (24 MHz) a permis de suivre des tumeurs renales chez la souris de diametre > 5 mm pour l’initiation du traitement (placebo/anti-angiogenique). L’echographie de contraste a ete realisee ensuite tous les 4 - 5 jours (systeme clinique). Dans le plan presentant la plus grande surface tumorale les evaluations morphologiques (dimensions) et fonctionnelle (l’intensite du contraste et la vitesse de remplissage suite a sa destruction acoustique - toujours dans la meme zone de profondeur) ont ete effectuees. L’echographie haute-resolution permet d’initier le traitement apres detection. Des reponses therapeutiques ont ete detectees plus precocement sur les mesures fonctionnelles que sur les mesures morphologiques.
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- 2008
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38. Valeurs prédictives desexpressions deHIF-1 alpha, HIF-2 alpha etCA IX parlesadénocarcinomes delaprostate traités parirradiation exclusive. Étude ancillaire duprotocole GETUG 06
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Pierre Bey, E. Comperat, V. Beckendorf, J.-M. Simon, P. Jaillon, and Jean-Jacques Mazeron
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Oncology ,business.industry ,Medicine ,Radiology, Nuclear Medicine and imaging ,business - Published
- 2007
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39. Tumeurs surrenaliennes : comment raisonne l’anatomo-pathologiste
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E. Comperat
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Radiological and Ultrasound Technology ,Radiology, Nuclear Medicine and imaging - Abstract
Resume Devant une tumeur de la surrenale, les problemes diagnostiques sont essentiellement de trois orders : distinguer une tumeur primitive d’une lesion metastatique ; en cas de tumeur primitive, distinguer les tumeurs du cortex des tumeurs de la medullaire et d’autres entites tumorales plus rares ; enfin dans le cas d’une tumeur surrenalienne corticale ou medullaire primitive, reconnaitre les elements en faveur d’une lesion benigne ou au contraire maligne. En dehors des origines renales qui constituent un piege classique, le diagnostic differentiel entre lesion surrenalienne primitive et metastatique est facilite par la connaissance du contexte clinique. L’analyse immunohistochimique permet habituellement de confirmer l’origine d’une lesion secondaire au sein de la surrenale. Devant une lesion corticale unique, bien limitee, de couleur chamois ou jaunâtre, accompagnee de manifestations cliniques a type d’hypercorticisme ou un syndrome de Cushing, le premier diagnostic a evoquer est celui d’un adenome surrenalien. Mais l’hyperplasie surrenalienne peut parfois prendre un aspect nodulaire ou diffus meme si elle atteint le plus souvent l’ensemble de la glande ou est bilaterale. Les kystes, epitheliaux, endotheliaux ou parasitaires (hydatidose, echinoccocose) et les autres neoplasies mesenchymateuses, notamment le myelolipome, sont generalement d’aspect radiologique evocateur. Les pheochromocytomes constituent les principales lesions de la medullaire. Parmi les autres tumeurs dans cette localisation, on observe des proliferations neurogenes comme les neuroblastomes. L’hyperplasie est egalement decrite. La distinction entre tumeur primitive benigne et maligne peut etre delicate en l’absence de metastase d’emblee. Les tumeurs malignes presentent souvent des zones de necrose, mais une tumeur benigne de grande taille peut etre siege de remaniements kystiques et hemorragiques. La distinction histologique se fonde sur l’analyse de criteres (dits de Weiss ou Weiss modifie). Des recidives tardives, meme 5 a 10 ans apres la tumeur initiale, ont ete rapportees. Chez l’enfant, des pheochromocytomes malins multiples ont ete rapportes soulignant l’importance des donnees de l’analyse moleculaire dans ces lesions pouvant entrer dans des syndromes complexes. Les donnees de l’imagerie et de l’anatomie pathologique apparaissent donc complementaires dans la prise en charge diagnostique et therapeutique de ces lesions dont l’incidence des decouvertes fortuites est en augmentation.
- Published
- 2006
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40. Atteinte tumorale du retroperitoine : aspects anatomo-pathologiques
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A. Vleillefond and E. Comperat
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Radiological and Ultrasound Technology ,Radiology, Nuclear Medicine and imaging - Abstract
Resume Le RP peut heberger pratiquement tous les types de proliferations tumorales. L’imagerie ne permet pas toujours d’apporter le diagnostic differentiel entre une lesion primitive ou secondaire (lymphome primitif versus metastase ganglionnaire, extension d’un carcinome de haut grade du rein, du pancreas, de la surrenale), ni entre une lesion benigne ou maligne (ex fibrose retroperitoneale idiopathique ou carcinose). La semiologie radiologique (mode developpement, contenu) compte tenu de la frequence des differentes tumeurs permet d’envisager un diagnostic de tumeur benigne tel que lymphangiome kystique, neurofibrome ou paragangliome ou de tumeur maligne (liposarcome le plus frequent). Mais il peut s’agir de tout autre type de sarcome (leiomyosarcome, angiosarcome, synovialosarcome.), ou d’une proliferation conjonctive de pronostic incertain (tumeur fibreuse solitaire, angiomyolipome epithelioide.). Une biopsie percutanee peut etre tres utile a condition qu’elle soit faite en concertation avec le pathologiste pour prevoir sur un materiel limite les etudes complementaires utiles : immunohistochimie (marqueurs lymphoi-des, musculaires, neuroides.,), une etude genomique (recherche d’anomalies cytogenetiques ou de transcrit de fusion). Ceci necessite que des prelevements soient congeles ou communiques frais au laboratoire de biologie moleculaire dans un milieu de transport (RPMI).
- Published
- 2004
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41. Expression of estrogen and progesterone receptors in breast metastases from malignant melanoma
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F. Cappuzzo, M. Spielmann, E. Comperat, M. Riofrio, and L. Zelek
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Oncology ,Cancer Research ,medicine.medical_specialty ,business.industry ,Estrogen ,medicine.drug_class ,Internal medicine ,Melanoma ,medicine ,business ,medicine.disease ,Receptor - Published
- 1999
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42. Metastases within the breast from extramammary primary solid tumors: a retrospective analysis
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M. Riofrio, L. Zelek, A. Ivanaj, M. Spielmann, C. Mathieu, E. Comperat, and F. Cappuzzo
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Cancer Research ,medicine.medical_specialty ,Primary (chemistry) ,Oncology ,business.industry ,Retrospective analysis ,Medicine ,Radiology ,business - Published
- 1999
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43. Metastin (KISS-1) and metastin-coupled receptor (GPR54) expression in transitional cell carcinoma of the bladder.
- Author
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G Nicolle, E Comperat, N Nicolaïew, G Cancel-Tassin, and O Cussenot
- Published
- 2007
- Full Text
- View/download PDF
44. Molecular Profiling of Sinonasal Adenoid Cystic Carcinoma: Canonical and Noncanonical Gene Fusions and Mutation.
- Author
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Skálová A, Bradová M, Agaimy A, Laco J, Badual C, Ihrler S, Damjanov I, Rupp NJ, Bacchi CE, Mueller S, Ventelä S, Zhang D, Comperat E, Martínek P, Šíma R, Vaněček T, Grossmann P, Steiner P, Hájková V, Kovářová I, Michal M, and Leivo I
- Abstract
Adenoid cystic carcinomas (AdCC) of salivary gland origin have long been categorized as fusion-defined carcinomas owing to the almost universal presence of the gene fusion MYB::NFIB, or less commonly MYBL1::NFIB. Sinonasal AdCC is an aggressive salivary gland malignancy with no effective systemic therapy. Therefore, it is urgent to search for potentially targetable genetic alterations associated with AdCC. We have searched the authors' registries and selected all AdCCs arising in the sinonasal tract. The tumors were examined histologically, immunohistochemically, by next generation sequencing (NGS) and/or fluorescence in situ hybridization (FISH) looking for MYB/MYBL1 and/or NFIB gene fusions or any novel gene fusions and/or mutations. In addition, all tumors were tested for HPV by genotyping using (q)PCR. Our cohort comprised 88 cases of sinonasal AdCC, predominantly characterized by canonical MYB::NFIB (49 cases) and MYBL1::NFIB (9 cases) fusions. In addition, noncanonical fusions EWSR1::MYB; ACTB::MYB; ESRRG::DNM3, and ACTN4::MYB were identified by NGS, each of them in 1 case. Among nine fusion-negative AdCCs, FISH detected rearrangements in MYB (7 cases), NFIB (1 case), and EWSR1 (1 case). Six AdCCs lacked fusions or gene rearrangements, while 11 cases were unanalyzable. Mutational analysis was performed by NGS in 31/88 (35%) AdCCs. Mutations in genes with established roles in oncogenesis were identified in 21/31 tumors (68%), including BCOR (4/21; 19%), NOTCH1 (3/21; 14%), EP300 (3/21; 14%), SMARCA4 (2/21; 9%), RUNX1 (2/21; 9%), KDM6A (2/21; 9%), SPEN (2/21; 9%), and RIT1, MGA, RB1, PHF6, PTEN, CREBBP, DDX41, CHD2, ROS1, TAF1, CCD1, NF1, PALB2, AVCR1B, ARID1A, PPM1D, LZTR1, GEN1, PDGFRA, each in 1 case (1/21; 5%). Additional 24 cases exhibited a spectrum of gene mutations of uncertain pathogenetic significance. No morphologic differences were observed between AdCCs with MYBL1::NFIB and MYB::NFIB fusions. Interestingly, mutations in the NOTCH genes were seen in connection with both canonical and noncanonical fusions, and often associated with high-grade histology or metatypical phenotype, as well as with poorer clinical outcome. Noncanonical fusions were predominantly observed in metatypical AdCCs. These findings emphasize the value of comprehensive molecular profiling in correlating morphologic characteristics, genetic landscape, and clinical behavior in AdCC., (Copyright © 2025 The Author(s). Published by Wolters Kluwer Health, Inc.)
- Published
- 2025
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45. Variation in cystectomy pathology reporting practice-results from an international survey of 212 pathologists.
- Author
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Griffin J, Hartmann A, and Comperat E
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- Humans, Practice Patterns, Physicians' statistics & numerical data, Pathology, Surgical methods, Neoplasm, Residual pathology, Tissue Fixation methods, Health Care Surveys, Surveys and Questionnaires, Cystectomy, Urinary Bladder Neoplasms pathology, Urinary Bladder Neoplasms surgery, Pathologists
- Abstract
The pathological assessment of cystectomy specimens is important for accurate prognostic information and to inform adjuvant therapy decisions. However, there is limited evidence regarding the best approach to fixation, dissection, block selection and microscopic assessment of cystectomies. We report the results of an international survey of 212 pathologists and their approach to cystectomy pathology. There is variation at all stages of the specimen journey including in fixation and dissection techniques, and in the approach to evaluating residual tumour. This is particularly evident in the post-neoadjuvant chemotherapy setting where there is variable use of response scoring systems and differing approaches to sampling. We also find variation in the use of digital and molecular pathology in cystectomy specimens. Finally, we have suggested areas for future research in cystectomy pathological assessment., Competing Interests: Declarations All participants gave informed consent to complete the questionnaire and the study received ethical approval from the University of Sheffield (UK) Ethics Committee on 24th July 2023 (approval number: 054611). Competing interests The authors declare no competing interests., (© 2024. The Author(s).)
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- 2024
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46. Final Results of the ANDROCAN Study: Histopathological Characteristics and Biochemical Recurrence at 5 Years of Localized Prostate Cancer According to Preoperative Gonadal Status.
- Author
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Neuzillet Y, Raynaud JP, Dreyfus JF, Radulescu C, Rouanne M, Schneider M, Krish S, Rouprêt M, Drouin SJ, Comperat E, Galiano M, Cathelineau X, Validire P, Molinié V, Fiet J, Giton F, Lebret T, and Botto H
- Abstract
Background and Objective: Failure rates after first-line treatment of localized prostate cancer (PCa) treatment remain high; therefore, it is essential to improve the selection and identification of at-risk patients to reduce mortality. The aim of the ANDROCAN study was to evaluate the biochemical recurrence (BCR) in patients with localized PCa treated by total prostatectomy at 5 yr after surgery, according to their presurgery gonadal status., Methods: A prospective cohort study was conducted including 1318 patients undergoing total prostatectomy for localized PCa with a 5-yr postoperative follow-up. Clinical and hormonal data (assays of total testosterone [TT], bioavailable testosterone [BT], dihydrotestosterone, estrone, and estradiol were performed by gas chromatography/mass spectrometry) as well as metabolic syndrome parameters were collected at baseline before surgery. Pathological data (predominant Gleason grade 4 and stage) were collected and cross-referenced centrally. Factors associated with BCR were assessed by a multivariate analysis, and BCR-free survival was assessed by a Kaplan-Meier analysis., Key Findings and Limitations: Among the 1318 patients, 237 had BCR of PCa. Considering demographic characteristics, populations with and without BCR were similar. However, patients with BCR had cancers with a higher Gleason score (p = 0.0001) and higher prostate-specific antigen (PSA) values (p = 0.0005) at baseline. Gleason score, pT >3a, and PSA level at baseline were positively correlated with BCR (p < 0.0001, p < 0.0001, and p = 0.0048, respectively), while BT and TT levels were not associated with BCR. This study includes patients with varying clinical characteristics, such as cancer history and metabolic syndrome, introducing variability that makes it challenging to isolate the specific effects of gonadal status on BCR. Another limitation is the lack of evaluation of long-term BCR beyond 5 yr, potentially overlooking recurrences that occur between 5 and 15 yr after surgery. This could lead to an underestimation of the actual long-term recurrence rates., Conclusions and Clinical Implications: Overall, PSA levels, high Gleason score, and pT >3a are associated with a greater likelihood of disease recurrence following initial treatment and could serve as important prognostic indicators for predicting the risk of BCR. In this prospective study, biochemical hypogonadism was not associated with a higher occurrence of BCR within 5 yr of prostatectomy. The biological gonadal status of preoperative patients could potentially be useful for therapeutic decisions but does not provide an indication for the oncological follow-up., Patient Summary: Five-year follow up of patients after surgery showed that there is no association between hypogonadism (low levels of total testosterone and bioavailable testosterone) and cancer recurrence. However, cancer recurrence seems to be more associated with aggressiveness of cancer at the time of detection., (Copyright © 2024 European Association of Urology. Published by Elsevier B.V. All rights reserved.)
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- 2024
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47. Renal cell carcinoma: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up.
- Author
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Powles T, Albiges L, Bex A, Comperat E, Grünwald V, Kanesvaran R, Kitamura H, McKay R, Porta C, Procopio G, Schmidinger M, Suarez C, Teoh J, de Velasco G, Young M, and Gillessen S
- Subjects
- Humans, Follow-Up Studies, Europe epidemiology, Carcinoma, Renal Cell therapy, Carcinoma, Renal Cell diagnosis, Carcinoma, Renal Cell pathology, Kidney Neoplasms therapy, Kidney Neoplasms diagnosis, Kidney Neoplasms pathology, Neoplasm Staging
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- 2024
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48. Neoadjuvant Cisplatin, Gemcitabine, and Docetaxel in Sarcomatoid Bladder Cancer: Clinical Activity and Whole Transcriptome Analysis.
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Johnson Iii BA, Teply BA, Kagemann C, McGuire B, Lombardo K, Jing Y, Langbo W, Epstein JI, Netto GJ, Baras AS, Matoso A, McConkey DJ, Gupta A, Ahuja N, Ross AE, Pierorazio PM, Comperat E, Hoffman-Censits J, Singla N, Patel SH, Kates M, Choi W, Bivalacqua TJ, and Hahn NM
- Abstract
Background: Sarcomatoid urothelial cancer of the bladder (SBC) is a rare, but aggressive histological subtype for which novel treatments are needed., Objective: We evaluated the clinical activity and safety of neoadjuvant cisplatin plus gemcitabine plus docetaxel (CGD) in muscle-invasive patients with SBC and assessed SBC tumor biology by whole transcriptome RNA sequencing., Methods: A single-institution, retrospective analysis of muscle-invasive SBC patients treated with neoadjuvant CGD with molecular analysis. Patients received cisplatin 35 mg/m2 + gemcitabine 800 mg/m2 + docetaxel 35 mg/m2 intravenously on days 1 and 8 + pegfilgrastim 6 mg subcutaneously on day 9 every 3 weeks for 4 cycles followed by cystectomy. The primary endpoint was pathologic complete response (ypCR) rate., Results: Sixteen patients with SBC received neoadjuvant CGD with a ypCR rate of 38% and a < ypT2 rate of 50%. Grade 3 and 4 toxicity occurred in 80% and 40% of patients, but was manageable with 81% of patients completing > 3 CGD cycles. Whole transcriptome RNA sequencing demonstrates co-clustering of SBC with conventional urothelial tumors. SBC tumors are characterized by basal-squamous and stroma rich gene signatures with frequent increased expression of immune checkpoint ( CD274 (PD-L1)), chemokine ( CXCL9 ), and T-cell ( CD8A ) genes., Conclusions: SBC is a chemosensitive subtype, with ypCR rate similar to urothelial bladder cancer following CGD neoadjuvant therapy. Whole transcriptome tissue analyses demonstrate increased expression of immune checkpoint and T-cell genes with therapeutic implications., Competing Interests: Noah Hahn discloses consulting compensation from AstraZeneca, Merck, BioGears, Seattle Genetics, Mirati, Incyte, RemGen, Janssen, Pfizer, EMD Serono, Verity Pharmaceuticals, Huron Consulting, Guidepoint, Natera, Protara Therapeutics, Astellas Pharma, Trya Biosciences; research support to the institution from HTG Molecular Diagnostics, AstraZeneca, Bristol Myers-Squibb, Genentech, Seattle Genetics, Pieris, Inovio, Principia Biopharm, Incyte, Loxo Oncology, and Ikena Oncology; speaking honorarium from Medscape. Max Kates discloses consulting compensation from Genesis Biotech, Janssen, Pacific Edge, and FerGene. Andres Matoso discloses consulting compensation from PathAI. Burles A. Johnson III discloses serving as an unpaid member of Seattle Genetics Emerging Thought Leaders Advisory Board. Burles A. Johnson III, Noah Hahn, Jean Hoffman-Censits, and David McConkey are co-authors on a provisional US patent for an immune-based biomarker to predict response to immunotherapy in patients with advanced bladder cancer. T.J.B., J.H-C., N.M.H., and D.J.M. are on the Editorial Board of this journal, but these individuals were not involved in the peer-review process nor had access to any information regarding its peer-review., (© 2024 – The authors. Published by IOS Press.)
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- 2024
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49. ESMO Clinical Practice Guideline interim update on first-line therapy in advanced urothelial carcinoma.
- Author
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Powles T, Bellmunt J, Comperat E, De Santis M, Huddart R, Loriot Y, Necchi A, Valderrama BP, Ravaud A, Shariat SF, Szabados B, van der Heijden MS, and Gillessen S
- Subjects
- Humans, Urologic Neoplasms drug therapy, Urologic Neoplasms pathology, Urinary Bladder Neoplasms drug therapy, Urinary Bladder Neoplasms pathology, Urinary Bladder Neoplasms therapy, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Carcinoma, Transitional Cell drug therapy, Carcinoma, Transitional Cell pathology
- Abstract
Competing Interests: Disclosure TP reports personal fees for advisory board membership from Astellas, AstraZeneca, Bristol Myers Squibb (BMS), Eisai, Exelixis, Incyte, Ipsen, Johnson & Johnson, Merck, Merck Serono, MSD, Novartis, Pfizer, Roche and Seattle Genetics; personal travel grants from AstraZeneca, Ipsen, MSD, Pfizer and Roche; personal sponsorship for the Uromigos Podcast from Mashup Ltd; institutional honoraria from Gilead; and institutional research grants from Astellas, AstraZeneca, BMS, Eisai, Exelixis, Ipsen, Johnson & Johnson, Merck, Merck Serono, MSD, Novartis, Pfizer, Roche and Seattle Genetics. JB reports personal fees for advisory board membership from AstraZeneca (bladder cancer), BMS (adjuvant study CM 247), Merck (bladder cancer) and Pfizer (global); personal fees as an invited speaker from Merck (lectures in national meetings) and MSD (ESMO Asia Congress 2020); personal stocks/shares in Bicycle; personal royalties as Section Editor for bladder cancer from UpToDate; institutional fees as coordinating principal investigator (PI) of the INDUCOMAIN trial from MSD and of a prostate cancer study of avelumab plus carboplatin from Pfizer, both through the Asia Pacific Regional Office (APRO) Association; and non-renumerated membership of the IMvigor011 study Steering Committee (Genentech) and the American Society of Clinical Oncology (ASCO). EC reports personal fees as an invited speaker from Janssen; and a non-renumerated advisory role as a consulting pathologist for the European Association of Urology (EAU) guidelines for bladder cancer. MDS reports fees from 4D (personal for advisory board membership; personal and institutional for Steering Committee membership and an advisory function), AAA (personal for advisory board and Steering Committee memberships), Amgen (personal for advisory board and Steering Committee memberships and an advisory function), Astellas (personal for advisory board membership, an advisory function and as an invited speaker; personal and institutional for Steering Committee membership and an advisory function), AstraZeneca (personal for advisory board and Steering Committee memberships and as an invited speaker; personal and institutional as coordinating PI and for an advisory function), Basilea (personal for advisory board membership; personal and institutional for Steering Committee membership, an advisory function, clinical trials and as local PI), Bayer (personal for advisory board membership; personal and institutional for Steering Committee membership and an advisory function), Bioclin (personal for advisory board membership, advisory functions and as an invited speaker), BMS (personal for advisory board membership; personal and institutional for Steering Committee membership, an advisory function and travel grants), Calithera (institutional as local PI), Eisai (personal for advisory board membership; personal and institutional as local PI, for an advisory function and clinical trials), Ferring (personal for advisory board membership and an advisory function), Gilead (personal for advisory board membership; personal and institutional for Steering Committee membership), Immunomedics/Gilead (personal for advisory board membership; personal and institutional for Steering Committee membership, an advisory function and as local PI), Ipsen (personal for advisory board membership; personal and institutional for Steering Committee membership and an advisory function), Janssen (personal as an invited speaker; personal and institutional for Steering Committee membership and an advisory function), Merck/Serono (personal for advisory board membership; personal and institutional for Steering Committee membership and an advisory function), MSD (personal for advisory board membership and as an invited speaker; personal and institutional for Steering Committee membership, an advisory function, clinical trials and as local PI), Nektar (institutional for clinical trials and as local PI), Novartis/Sandoz (personal for advisory board membership; personal and institutional for Steering Committee membership and advisory function), Pierre Fabre (personal for advisory board membership and as an invited speaker personal and institutional for Steering Committee membership, an advisory function and as local and coordinating PI), Roche (personal for advisory board membership), Roche/Genentech (personal and institutional for Steering Committee membership and an advisory function), Sandoz (personal for Steering Committee membership and an advisory function), Sanofi (personal for advisory board membership; personal and institutional for Steering Committee membership and an advisory function), Seagen (personal for advisory board membership; personal and institutional for Steering Committee membership, an advisory function and as local PI); and non-renumerated membership of the EAU guidelines group for prostate cancer (writing and discussing guidelines for treatment and diagnostics), the ESMO CPGs author group for bladder cancer and the S3-Leitlinie Blasenkrebs (guidelines for the treatment of bladder cancer). RH reports personal fees for advisory board membership from Astellas, BioNTech, BMS, Merck, MSD, Nektar and Roche; personal fees as an invited speaker from Pfizer and Roche; personal fees for expert testimony from the National Institute of Clinical Excellence; personal and institutional fees for Steering Committee membership from Janssen and Nektar; personal fees for consultancy from Roche; personal fees for a limited liability partnership from the Cancer Centre London; institutional royalties from Janssen; institutional fees as a local PI from Astellas, Basilea, Bicycle, Gilead, Janssen, MSD, Nektar and Roche; institutional fees as a coordinating PI from Cancer Research UK (CRUK); institutional research grants from MSD and Roche; non-renumerated roles as chief investigator or co-investigator on CRUK-funded studies; non-renumerated roles as educational secretary and trustee of the British Uro-oncology group; a non-renumerated role as chair of the NCRI Clinical and Translational Radiotherapy Research Working Group (CTRad); and non-renumerated membership of the consensus guideline group of the Royal College of Radiologists. YL reports personal fees for advisory board membership from Gilead, Merck KGaA, Pfizer, Seattle Genetics and Taiho; personal fees for advisory board membership and lectures from Astellas, AstraZeneca, BMS, Janssen, MSD and Roche; personal fees for Steering Committee membership from Basilea; institutional fees as a local PI from Astellas, AstraZeneca, BMS, Exelixis, Gilead, Incyte, Janssen, Merck KGaA, MSD and Pfizer; institutional fees for Steering Committee membership and as a coordinating PI from Janssen; institutional research grants from Celsius, Janssen, MSD, Roche and Sanofi; Steering Committee membership for Astellas, Gilead/Immunomedics, MSD and Taiho; and non-renumerated memberships of the American Association for Cancer Research (AACR), the Scientific Committee of Fondation ARC, ASCO and ESMO. AN reports personal fees for Steering Committee membership from Astellas, AstraZeneca, Bayer, Clovis Oncology, Janssen, Merck and Roche; institutional research grants from AstraZeneca, BMS, Gilead, Ipsen and Merck; a role as coordinating PI for Incyte; a role as local PI for Pfizer; and a non-renumerated leadership role for the Global Society of Rare Genitourinary Tumors (GSRGT). BPV reports personal fees for advisory board membership from AAA, Astellas Pharma, AstraZeneca, BMS, EUSA Pharma, Ipsen, Merck, MSD, Pfizer and Recordati; personal fees as an invited speaker from AAA, Almirall Pharma, Astellas Pharma, Bayer, BMS, Merck, MSD and Pfizer; and travel grants from BMS and Pfizer. AR reports personal fees for advisory board membership from AstraZeneca, BMS, Ipsen, Merck GA and Pfizer; institutional research grants from Ipsen, Merck GA and Pfizer; institutional fees as local PI from AstraZeneca, BMS, Ipsen, Merck GA and Pfizer; travel grants/accommodation compensation for meetings/conferences from BMS, Ipsen, Merck GA and Pfizer; and a non-renumerated role as affiliate of ASCO. SFS reports personal fees for advisory board membership from Astellas, AstraZeneca, Bayer, BMS, Cepheid, Ferring, Ipsen, Janssen, Lilly, MSD, Olympus, Pfizer, Pierre Fabre, Richard Wolf, Roche, Sanochemia, Sanofi, Takeda and UroGen. BS reports personal fees for advisory board membership from Merck KGaA; personal fees as an invited speaker from MSD and Pfizer; personal fees for expert testimony from Ellipses and Ipsen; and personal travel grants from Photocure and Roche/Genentech. MSvdH reports institutional fees for advisory board membership from AstraZeneca, BMS, Janssen, MSD, Pfizer and Seagen; institutional funding for investigator-initiated trials from 4SC, AstraZeneca, BMS and Roche; institutional fees for Steering Committee membership and as local PI from AstraZeneca, BMS, MSD and Seagen; and institutional fees as local and study co-PI from Janssen. SG reports personal fees as an invited speaker for DESO, ESMO, Meister ConCept GmbH and the Swiss Group for Clinical Cancer Research (SAKK); personal travel grants from AstraZeneca, Bayer, Gilead and Intellisphere LLC; a patent for a biomarker of Proteomedix/Onconetix; institutional fees for advisory board membership from Amgen, AstraZeneca, Bayer, BMS, Boehringer Ingelheim, Daiichi Sankyo, Innomedica, Ipsen, Macrogenics, MSD Merck Sharp & Dohme, Myriad Genetics and Orion; institutional fees as an invited speaker for AdMeTech Foundation, ASCO GU, EPG Health, ESMO, Intellisphere LLC, Meister ConCept GmbH, S. Grasso Consulting, SAKK and Silvio Grasso Consulting; institutional funding as a co-investigator from Astellas; other institutional fees from PeerVoice (interview), Pfizer (Scientific Committee Pfizer Forschungspreis), TOLREMO (consulting) and WebMD-Medscape (faculty activity); and a non-remunerated advisory role for ProteoMediX.
- Published
- 2024
- Full Text
- View/download PDF
50. Tumour-based Mutational Profiles Predict Visceral Metastasis Outcome and Early Death in Prostate Cancer Patients.
- Author
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Cussenot O, Timms KM, Perrot E, Blanchet P, Brureau L, Solimeno C, Fromont G, Comperat E, and Cancel-Tassin G
- Subjects
- Humans, Male, Aged, Middle Aged, Aged, 80 and over, Adenomatous Polyposis Coli Protein genetics, beta Catenin genetics, Tumor Suppressor Protein p53 genetics, Prognosis, BRCA2 Protein genetics, Kaplan-Meier Estimate, Bone Neoplasms secondary, Bone Neoplasms genetics, Bone Neoplasms mortality, Neoplasm Metastasis, Proportional Hazards Models, Lymphatic Metastasis genetics, Microsatellite Instability, Prostatic Neoplasms genetics, Prostatic Neoplasms pathology, Prostatic Neoplasms mortality, Mutation
- Abstract
Background: Visceral metastases are known to occur in advanced prostate cancer, usually when the tumour is resistant to androgen deprivation and, have worse outcomes regardless of therapies., Objective: To analyse genomic alterations in tumour samples according to their lymphatic, bone, and visceral metastatic stages and overall survival., Design, Setting, and Participants: We selected 200 patients with metastatic prostate cancer. Genomic profiling of 111 genes and molecular signatures (homologous recombination deficiency [HRD], microsatellite instability, and tumour burden mutation) was performed with the MyChoice test (Myriad Genetics, Inc, Salt Lake City, UT, USA)., Outcome Measurements and Statistical Analysis: The association between genomic profiles and visceral metastatic evolution was evaluated using logistic regression. Kaplan-Meier and Cox proportional hazard analyses were used for analyses of early death., Results and Limitations: A total of 173 (87%) genomic profiles were obtained. Eighty-four (49%) patients died during the follow-up period (median duration = 76 mo). TP53 was the most frequently mutated gene, followed by FANC genes, including BRCA2, and those of the Wnt-pathway (APC/CTNNB1). TP53 gene mutations were more frequent in patients of European (42%) than in those of African (16%) ancestry. An HRD score of >25 was predictive of FANC gene mutations. The mutational status of TP53 (p < 0.001) and APC (p = 0.002) genes were significantly associated with the risk of visceral metastases. The mutational status of CTNNB1 (p = 0.001), TP53 (p = 0.015), BRCA2 (p = 0.027), and FANC (p = 0.005) genes were significantly associated with an earlier age at death. The limitations are the retrospective study design based on a selection of genes and the low frequency of certain molecular events., Conclusions: Mutations in the TP53 gene and genes (APC/CTNNB1) related to the Wnt pathway are associated with metastatic visceral dissemination and early death. These genomic alterations could be considered as markers to identify prostate cancer patients at a high risk of life-threatening disease who might benefit from more intensified treatment or new targeted therapies., Patient Summary: In this report, we evaluated the relationships between genomic profiles (gene mutations and molecular signatures) of tumour samples from patients with metastatic prostate cancer and early death. We found that mutations of specific genes, notably TP53 and APC/CTNNB1 related to the Wnt pathway, are associated with visceral metastatic progression and an earlier age at death., (Copyright © 2023 European Association of Urology. Published by Elsevier B.V. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
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