Activity endpoints reported in soft tissue sarcoma phase II trials: Quality of reported endpoints and correlation with overall survival

被引:8
作者
Penel, Nicolas [1 ,2 ]
Cousin, Sophie [1 ]
Duhamel, Alain [2 ]
Kramar, Andrew [2 ,3 ]
机构
[1] Ctr Oscar Lambret, Dept Gen Oncol, F-59020 Lille, France
[2] Lille Nord de France Univ, Sch Med, EA 2694, Unit Res, Lille, France
[3] Ctr Oscar Lambret, Methodol & Biostat Unit, F-59020 Lille, France
关键词
Phase II trials; Activity endpoint; Correlation; Advanced soft tissue sarcoma; EUROPEAN ORGANIZATION; RESPONSE EVALUATION; PROGRESSION-FREE; PAZOPANIB; DISEASE; DESIGN;
D O I
10.1016/j.critrevonc.2013.05.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Despite extensive research over the past 3 decades, few investigational drugs are considered as promising and these drugs failed to improve overall survival. Therefore we performed a systematic review of the literature to improve our understanding of the reasons that explain these failures. Methods: We reviewed 53 phase II trial reports that investigated new treatments in patients with advanced soft tissue sarcoma from 1999 to 2011. We critically reviewed the selected primary endpoint used in these trials. Results: Forty percent of trials were not interpretable because of major inherent methodological flaws. Only 3 primary endpoints were correlated with median overall survival (mOS): 3- and 6-month progression free rates and median progression-free survival. Nevertheless, the mOS was not significantly higher in the cases of active drugs. Discussion: We need to improve the definition of primary active endpoints and develop better designs for future trials. The current definition of promising drugs must be refined. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:309 / 317
页数:9
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