Phase 3 Trial of Everolimus for Metastatic Renal Cell Carcinoma Final Results and Analysis of Prognostic Factors

被引:979
作者
Motzer, Robert J. [1 ]
Escudier, Bernard [2 ]
Oudard, Stephane [3 ]
Hutson, Thomas E. [4 ]
Porta, Camillo [5 ]
Bracarda, Sergio [6 ]
Grunwald, Viktor [7 ]
Thompson, John A. [8 ]
Figlin, Robert A. [9 ]
Hollaender, Norbert [10 ]
Kay, Andrea [11 ]
Ravaud, Alain [12 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Genitourinary Oncol Serv, Dept Med, New York, NY 10021 USA
[2] Inst Gustave Roussy, Immunotherapy Unit, Villejuif, France
[3] Georges Pompidou Hosp, Oncol Translat Res Unit, Paris, France
[4] US Oncol Baylor Sammons Canc Ctr, Dallas, TX USA
[5] IRCCS, San Matteo Univ Hosp Fdn, Pavia, Italy
[6] San Donato Hosp, Arezzo, Italy
[7] Hannover Med Sch, Clin Hematol Hemostaseol Oncol & Stem Cell Transp, D-3000 Hannover, Germany
[8] Seattle Canc Care Alliance, Seattle, WA USA
[9] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[10] Novartis Oncol, Basel, Switzerland
[11] Novartis Oncol, Florham Pk, NJ USA
[12] St Andre CHU Hosp, Bordeaux, France
关键词
everolimus; metastatic renal cell carcinoma; phase; 3; prognostic factors; RAD001; RANDOMIZED-TRIALS; NONCOMPLIANCE; MTOR;
D O I
10.1002/cncr.25219
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: A phase 3 trial demonstrated superiority at interim analysis for everolimus over placebo in patients with metastatic renal cell carcinoma (mRCC) progressing on vascular endothelial growth factor receptor-tyrosine kinase inhibitors. Final results and analysis of prognostic factors are reported. METHODS: Patients with mRCC (N = 416) were randomized (2:1) to everolimus 10 mg/d (n = 277) or placebo (n = 139) plus best supportive care. Progression-free survival (PFS) and safety were assessed to the end of double-blind treatment. Mature overall survival (OS) data were analyzed, and prognostic factors for survival were investigated by multivariate analyses. A rank-preserving structural failure time model estimated the effect on OS, correcting for crossover from placebo to everolimus. RESULTS: The median PFS was 4.9 months (everolimus) versus 1.9 months (placebo) (hazard ratio [HR], 0.33; P < .001) by independent central review and 5.5 months (everolimus) versus 1.9 months (placebo) (HR, 0.32; P < .001) by investigators. Serious adverse events with everolimus, independent of causality, in >= 5% of patients included infections (all types, 10%), dyspnea (7%), and fatigue (5%). The median OS was 14.8 months (everolimus) versus 14.4 months (placebo) (HR, 0.87; P = .162), with 80% of patients in the placebo arm crossed over to everolimus. By the rank-preserving structural failure time model, the survival corrected for crossover was 1.9-fold longer (95% confidence interval, 0.5-8.5) with everolimus compared with placebo only. Independent prognostic factors for shorter OS in the study included low performance status, high corrected calcium, low hemoglobin, and prior sunitinib (P < .01). CONCLUSIONS: These results established the efficacy and safety of everolimus in patients with mRCC after progression on sunitinib and/or sorafenib. Cancer 2010;116:4256-65. (C) 2010 American Cancer Society.
引用
收藏
页码:4256 / 4265
页数:10
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