Journal of Clinical Oncology, Vol 23, No 12 (April 20), 2005: pp. 2763-2771
© 2005 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2005.07.055
Prognostic Value of Histologic Subtypes in Renal Cell Carcinoma: A Multicenter Experience
Jean-Jacques Patard,
Emmanuelle Leray,
Nathalie Rioux-Leclercq,
Luca Cindolo,
Vincenzo Ficarra,
Amnon Zisman,
Alexandre De La Taille,
Jacques Tostain,
Walter Artibani,
Claude C. Abbou,
Bernard Lobel,
François Guillé,
Dominique K. Chopin,
Peter F.A. Mulders,
Christopher G. Wood,
David A. Swanson,
Robert A. Figlin,
Arie S. Belldegrun,
Allan J. Pantuck
From the Department of Urology; Department of Public Health; Department of Pathology, Rennes University Hospital, Rennes; Department of Urology, Centre Hospitalier Universitaire (CHU) Henri Mondor, Creteil; Department of Urology, North Hospital, CHU of Saint-Etienne, France; University of California, Los Angeles (UCLA) Department of Urology; Department of Biostatistics, UCLA School of Medicine, Los Angeles, CA; Department of Urology, Medical School of University Federico II, Naples; Department of Urology, University of Verona, Verona, Italy; University Medical Center Nijmegen, Nijmegen, the Netherlands
Address reprint requests to Allan J. Pantuck, MD, UCLA Department of Urology, CHS 66-118, 10833 LeConte Avenue, Los Angeles, CA 90095-1738; e-mail: APantuck{at}mednet.ucla.edu
PURPOSE: To analyze to what extent histologic subtype is of prognostic importance in renal cell carcinoma based on a large, international, multicenter experience.
PATIENTS AND METHODS: Four thousand sixty-three patients from eight international centers were included in this retrospective study. Histologic subtype (1997 International Union Against Cancer [UICC] criteria of tumor response), age, sex, TNM stage, Fuhrman grade, tumor size, Eastern Cooperative Oncology Goup performance status (ECOG PS), and overall survival were determined in all cases. The prognostic values of clear cell, papillary, and chromophobe histologic features were assessed by uni- and multivariate analysis using the Kaplan-Meier method and Cox model, respectively.
RESULTS: Clear cell, papillary, and chromophobe carcinomas accounted for 3,564 (87.7%), 396 (9.7%) and 103 (2.5%) cases, respectively. In univariate analysis, a trend toward a better survival was observed when clear cell, papillary, and chromophobe histologies were considered prognostic categories (log-rank P = .0007). However, in multivariate analysis, TNM stage, Fuhrman grade and ECOG PS, but not histology, were retained as independent prognostic variables (P < .001).
CONCLUSION: The stratification in three main renal cell carcinoma histologic subtypes as defined by the 1997 UICCAmerican Joint Committee on Cancer consensus should not be considered a major prognostic variable comparable to TNM stage, Fuhrman grade and ECOG PS.
Authors' disclosures of potential conflicts of interest are found at the end of this article.
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