Chromophobe renal cell carcinoma (RCC): Oncological outcomes and prognostic factors in a large multicentre series

Alessandro Volpe, Giacomo Novara, Alessandro Antonelli, Roberto Bertini, Michele Billia, Giorgio Carmignani, Sergio Cosciani Cunico, Nicola Longo, Guido Martignoni, Andrea Minervini, Vincenzo Mirone, Alchiede Simonato, Carlo Terrone, Filiberto Zattoni, Vincenzo Ficarra, O. De Cobelli, G. Martorana, R. Schiavina, S. Corti, C. SimeoneM. Castelli, S. Cimino, V. Favilla, G. Morgia, C. Imbimbo, M. Carini, L. Masieri, S. Serni, F. Oneto, V. Varca, F. Rocco, C. Valotto, E. Costantini, M. Porena, A. Zucchi, S. Ciciliato, N. Lampropoulou, S. Siracusano, D. Fontana, P. Gontero, A. Tizzani, W. Artibani, M. Brunelli, F. Montorsi, G. Petralia, M. Roscigno, E. Strada

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

OBJECTIVES: • To investigate cancer-related outcomes of chromophobe renal cell carcinoma (ChRCC) in a large multicentre dataset. • To determine prognostic factors for recurrence-free survival (RFS) and cancer-specific survival (CSS) for this RCC histological type. PATIENTS AND METHODS: • In all, 291 patients with ChRCC were identified from a multi-institutional retrospective database including 5463 patients who were surgically treated for RCC at 16 Italian academic centres between 1995 and 2007. • Univariable and multivariable Cox regression models were used to identify prognostic factors predictive of RFS and CSS after surgery for ChRCC. RESULTS: • At a median follow-up of 44 months, 25 patients (8.6%) had disease recurrence and 18 patients (6.2%) died from disease.• The 5-year RFS and CSS rates were 89.3% and 93%, respectively. • Gender ( P = 0.014), clinical T stage ( P = 0.017), pathological T stage ( P = 0.003), and sarcomatoid differentiation ( P = 0.032) were independent predictors of RFS at multivariable analysis. • For CSS, there was an independent prognostic role for gender ( P = 0.032) and T stage ( P = 0.019) among the clinical variables and for T stage ( P = 0.016), N/M stage ( P = 0.023), and sarcomatoid differentiation ( P = 0.015) among the pathological variables. CONCLUSIONS: • Patients with ChRCC have a low risk of tumour progression, metastasis, and cancer-specific death. • Patient gender, clinical and pathological tumour stage, and sarcomatoid differentiation are significant predictors of RFS and CSS for ChRCC.

Lingua originaleInglese
pagine (da-a)76-83
Numero di pagine8
RivistaBJU International
Volume110
Numero di pubblicazione1
DOI
Stato di pubblicazionePubblicato - lug 2012

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