Annals of Surgical Oncology Cite Track
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

10.1245/ASO.2004.06.016
Annals of Surgical Oncology 11:71-77 (2004)
© 2004 Society of Surgical Oncology
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Beck, S. D. W.
Right arrow Articles by Russo, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Beck, S. D. W.
Right arrow Articles by Russo, P.
Related Collections
Right arrow Prognostic factors
Right arrow Surgery

ORIGINAL ARTICLES

Effect of Papillary and Chromophobe Cell Type on Disease-Free Survival After Nephrectomy for Renal Cell Carcinoma

Stephen D. W. Beck, MD, Manish I. Patel, MD, Mark E. Snyder, BA, Michael W. Kattan, MD, Robert J. Motzer, MD, Victor E. Reuter, MD and Paul Russo, MD

From the Departments of Urology (SDWB, MIP, MES, PR), Epidemiology and Biostatistics (MWK), Medicine (RJM), and Pathology (VER), Memorial Sloan-Kettering Cancer Center, New York, New York.

Correspondence: Address correspondence and reprint requests to: Paul Russo, MD, Department of Urology, Sidney Kimmel Center for Prostate and Urologic Cancers, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021; Fax: 212-988-0760; E-mail: russop{at}mskcc.org

Background: The clinical staging of renal cortical tumors traditionally has not evaluated the potential effect of histological subtypes on survival. Evidence suggests that conventional clear cell renal cell carcinoma (RCC) and nonconventional clear cell RCC (chromophobe and papillary) have different metastatic potential. Using a large renal tumor database, we examined the effect of tumor histology on the pattern of metastasis and patient survival.

Methods: All patients with nonmetastatic renal cortical tumors undergoing partial or radical nephrectomy were identified from a renal tumor database between July 1989 and July 2002. Kaplan-Meier and Cox regression tests were used for statistical analysis.

Results: Analysis revealed 1057 patients: 794 with conventional clear cell RCC, 157 with papillary RCC, and 106 with chromophobe RCC. Metastasis occurred in 95 conventional clear cell RCC, 9 papillary RCC, and 6 chromophobe RCC with a median follow-up of 34.6, 43.0, and 33.2 months, respectively. Using log-rank analysis, chromophobe and papillary RCC were associated with an improved disease-free survival at 5 years (P = .009 and .015, respectively). Multivariate analysis revealed tumor size, stage, and chromophobe histology as significant variables for disease progression.

Conclusions: Renal cortical tumors have distinct histological subtypes with varying degrees of metastatic potential. Conventional clear cell RCC, which comprises two thirds of renal cortical tumors presenting with localized disease, has a less favorable outcome when compared with papillary and chromophobe RCC. Controlling for size and stage, chromophobe, and not papillary, RCC was a significant variable for disease progression compared with conventional clear cell RCC. Knowledge of renal cortical tumor histological subtype is critical for projecting prognosis, tailoring follow-up strategies, and designing clinical trials.

Key Words: Kidney cancer • Histology • Metastases • Staging




This article has been cited by other articles:


Home page
Am. J. Roentgenol.Home page
N. Griffin, M. E. Gore, and S. A. Sohaib
Imaging in Metastatic Renal Cell Carcinoma
Am. J. Roentgenol., August 1, 2007; 189(2): 360 - 370.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
J. Zhang, R. A. Lefkowitz, N. M. Ishill, L. Wang, C. S. Moskowitz, P. Russo, H. Eisenberg, and H. Hricak
Solid Renal Cortical Tumors: Differentiation with CT
Radiology, August 1, 2007; 244(2): 494 - 504.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
H. T. Cohen and F. J. McGovern
Renal-Cell Carcinoma
N. Engl. J. Med., December 8, 2005; 353(23): 2477 - 2490.
[Full Text] [PDF]


Home page
J. Mol. Diagn.Home page
A. N. Schuetz, Q. Yin-Goen, M. B. Amin, C. S. Moreno, C. Cohen, C. D. Hornsby, W. L. Yang, J. A. Petros, M. M. Issa, J. G. Pattaras, et al.
Molecular Classification of Renal Tumors by Gene Expression Profiling
J. Mol. Diagn., May 1, 2005; 7(2): 206 - 218.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
J.-J. Patard, E. Leray, N. Rioux-Leclercq, L. Cindolo, V. Ficarra, A. Zisman, A. De La Taille, J. Tostain, W. Artibani, C. C. Abbou, et al.
Prognostic Value of Histologic Subtypes in Renal Cell Carcinoma: A Multicenter Experience
J. Clin. Oncol., April 20, 2005; 23(12): 2763 - 2771.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
W. M. Stadler
Therapeutic Options for Variant Renal Cancer: A True Orphan Disease
Clin. Cancer Res., September 15, 2004; 10(18): 6393S - 6396S.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the Society of Surgical Oncology.