Validation and extension of the Memorial Sloan-Kettering prognostic factors model for survival in patients with previously untreated metastatic renal cell carcinoma

被引:415
作者
Mekhail, TM [1 ]
Abou-Jawde, RM [1 ]
BouMerhi, G [1 ]
Malhi, S [1 ]
Wood, L [1 ]
Elson, P [1 ]
Bukowski, R [1 ]
机构
[1] Cleveland Clin Fdn, Taussig Canc Ctr, Taussig Canc Ctr R35, Cleveland, OH 44195 USA
关键词
D O I
10.1200/JCO.2005.05.179
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To validate the Motzer et al prognostic factors model for survival in patients with previously untreated metastatic renal cell carcinoma (RCC) and to identify additional independent prognostic factors. Patients and Methods Data were collected on 353 previously untreated metastatic RCC patients enrolled onto clinical trials between 1987 and 2002. Results Four of the five prognostic factors identified by Motzer were independent predictors of survival. In addition, prior radiotherapy and presence of hepatic, lung, and retroperitoneal nodal metastases were found to be independent prognostic factors. Using the number of metastatic sites as surrogate for individual sites (none or one v two or three sites), Motzer's definitions of risk groups were expanded to accommodate these two additional prognostic factors. Using this expanded criteria, favorable risk is defined as zero or one poor prognostic factor, intermediate risk is two poor prognostic factors, and poor risk is more than two poor prognostic factors. According to Motzer's definitions, 19% of patients were favorable risk, 70% were intermediate risk, and 11% were poor risk; median overall survival times for these groups were 28.6, 14.6, and 4.5 months, respectively (P < .0001). Using the expanded criteria, 37% of patients were favorable risk, 35% were intermediate risk, and 28% were poor risk; median overall survival times of these groups were 26.0, 14.4, and 7.3 months, respectively (P < .0001). Conclusion These data validate the model described by Motzer et al. Additional independent prognostic factors identified were prior radiotherapy and sites of metastasis. Incorporation of these additional prognostic factors into the Motzer et al model can help better define favorable risk, intermediate risk, and poor risk patients.
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页码:832 / 841
页数:10
相关论文
共 39 条
[1]  
AGRAWAL N, 2002, P AN M AM SOC CLIN, V21, pB5
[2]   Metastatic renal carcinoma comprehensive prognostic system [J].
Atzpodien, J ;
Royston, P ;
Wandert, T ;
Reitz, M .
BRITISH JOURNAL OF CANCER, 2003, 88 (03) :348-353
[3]  
BUKOWSKI RM, 1991, CANCER RES, V51, P836
[4]   Phase II trial of interleukin-2 and interferon-alpha in patients with renal cell carcinoma: Clinical results and immunologic correlates of response [J].
Bukowski, RM ;
Olencki, T ;
Wang, Q ;
Peereboom, D ;
Budd, GT ;
Elson, P ;
Sandstrom, K ;
Tuason, L ;
Rayman, P ;
Tubbs, R ;
McLain, D ;
Klein, E ;
Novick, A ;
Finke, J .
JOURNAL OF IMMUNOTHERAPY, 1997, 20 (04) :301-311
[5]   Phase I trial of capecitabine in combination with interferon alpha in patients with metastatic renal cancer: toxicity and pharmacokinetics [J].
Chang, DZ ;
Olencki, T ;
Budd, GT ;
Peereboom, D ;
Ganapathi, R ;
Osterwalder, B ;
Bukowski, R .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2001, 48 (06) :493-498
[6]   Rising incidence of renal cell cancer in the United States [J].
Chow, WH ;
Devesa, SS ;
Warren, JL ;
Fraumeni, JF .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (17) :1628-1631
[7]  
Cox D.R., 1990, ANAL SURVIVAL DATA
[8]   PROGNOSTIC FACTORS OF ADULT METASTIC RENAL-CARCINOMA - A MULTIVARIATE-ANALYSIS [J].
DEFORGES, A ;
REY, A ;
KLINK, M ;
GHOSN, M ;
KRAMAR, A ;
DROZ, JP .
SEMINARS IN SURGICAL ONCOLOGY, 1988, 4 (03) :149-154
[9]  
ELSON PJ, 1988, CANCER RES, V48, P7310
[10]   Multicenter, randomized, phase III trial of CD8+ tumor-infiltrating lymphocytes in combination with recombinant interleukin-2 in metastatic renal cell carcinoma [J].
Figlin, RA ;
Thompson, JA ;
Bukowski, RM ;
Vogelzang, NJ ;
Novick, AC ;
Lange, P ;
Steinberg, GD ;
Belldegrun, AS .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (08) :2521-2529