A randomised, double-blind phase III study of pazopanib in patients with advanced and/or metastatic renal cell carcinoma: Final overall survival results and safety update

被引:356
|
作者
Sternberg, Cora N. [1 ,2 ]
Hawkins, Robert E. [3 ,4 ]
Wagstaff, John [5 ]
Salman, Pamela [6 ]
Mardiak, Jozef [7 ]
Barrios, Carlos H. [8 ]
Zarba, Juan J. [9 ]
Gladkov, Oleg A. [10 ]
Lee, Eunsik [11 ]
Szczylik, Cezary [12 ]
McCann, Lauren [13 ]
Rubin, Stephen D. [13 ]
Chen, Mei [13 ]
Davis, Ian D. [14 ]
机构
[1] San Camillo Hosp, Dept Med Oncol, I-00152 Rome, Italy
[2] Forlanini Hosp, Dept Med Oncol, I-00152 Rome, Italy
[3] Univ Manchester, Canc Res UK Dept Med Oncol, Manchester, Lancs, England
[4] Christie Hosp NHS Fdn Trust, Manchester, Lancs, England
[5] Singleton Hosp, South West Wales Canc Inst, Swansea SA2 8QA, W Glam, Wales
[6] Fdn Arturo Lopez Perez, Div Hematol & Med Oncol, Santiago, Chile
[7] Natl Oncol Inst, Bratislava, Slovakia
[8] PUCRS Sch Med, Oncol Serv, Oncol Res Unit, Porto Alegre, RS, Brazil
[9] Ctr Med San Roque, San Miguel De Tucuman, Argentina
[10] Chelyabinsk Reg Oncol Ctr, Chelyabinsk, Russia
[11] Seoul Natl Univ, Coll Med, Dept Urol, Seoul, South Korea
[12] Mil Inst Med, Dept Oncol, Warsaw, Poland
[13] GlaxoSmithKline, Collegeville, PA USA
[14] Austin Hlth, Ludwig Inst Canc Res, Joint Austin Ludwig Oncol Unit, Melbourne, Vic, Australia
关键词
Renal cell carcinoma; Pazopanib; Overall survival; Rank-preserving structural failure time model; Inverse probability of censor weighting; INTERFERON ALPHA-2A; INVERSE PROBABILITY; NONCOMPLIANCE; GUIDELINES; TRIALS;
D O I
10.1016/j.ejca.2012.12.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: In this randomised phase III study (VEG105192; NCT00334282), pazopanib previously demonstrated statistically and clinically meaningful improvement of progression-free survival versus placebo in patients with advanced/metastatic renal cell carcinoma (mRCC). Final overall survival (OS) and updated safety results are now reported. Methods: Treatment-naive or cytokine-pretreated mRCC patients (n = 435) stratified and randomised (2: 1) to pazopanib 800 mg daily or placebo, were treated until disease progression, death or unacceptable toxicity. Upon progression, placebo patients could receive pazopanib through an open-label study. Final OS in the intent-to-treat population was analysed using a stratified log-rank test. Rank-preserving structural failure time (RPSFT) and inverse probability of censoring weighted (IPCW) analyses were performed post-hoc to adjust for crossover. Findings: The difference in final OS between pazopanib- and placebo-treated patients was not statistically significant (22.9 versus 20.5 months, respectively; hazard ratio [HR] = 0.91; 95% confidence interval [CI], 0.71-1.16; one-sided P = .224). Early and frequent crossover from placebo to pazopanib and prolonged duration of crossover treatment confounded the OS analysis. In IPCW analyses, pazopanib decreased mortality (HR = 0.504; 95% CI, 0.315-0.762; two-sided P = .002). Similar, albeit non-significant, results were obtained in RPSFT analyses (HR = 0.43; 95% CI, 0.215-1.388; two-sided P = .172). Since the last cutoff, cumulative exposure to pazopanib increased by 30%. The pazopanib safety profile showed no new safety signals or changes in the type, frequency and severity of adverse events. Interpretation: Although no significant difference in OS was observed in this study, extensive crossover from placebo to pazopanib confounded final OS analysis. Post-hoc analyses adjusting for crossover suggest OS benefit with pazopanib treatment for mRCC patients. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1287 / 1296
页数:10
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