Blinded independent central review of progression-free survival in phase III clinical trials: Important design element or unnecessary expense?

被引:143
作者
Dodd, Lori E. [1 ]
Korn, Edward L.
Freidlin, Boris
Jaffe, C. Carl
Rubinstein, Lawrence V.
Dancey, Janet
Mooney, Margaret M.
机构
[1] NCI, Branch Biometr Res, Div Canc Treatment & Diag, Bethesda, MD 20892 USA
关键词
D O I
10.1200/JCO.2008.16.1711
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Progression-free survival is an important end point in advanced disease settings. Blinded independent central review (BICR) of progression in randomized clinical trials has been advocated to control bias that might result from errors in progression assessments. However, although BICR lessens some potential biases, it does not remove all biases from evaluations of treatment effectiveness. In fact, as typically conducted, BICRs may introduce bias because of informative censoring, which results from having to censor unconfirmed locally determined progressions. In this article, we discuss the rationale for BICR and different ways of implementing independent review. We discuss the limitations of these approaches and review published trials that report implementing BICR. We demonstrate the existence of informative censoring using data from a randomized phase II trial. We conclude that double-blinded trials with consistent application of measurement criteria are the best means of ensuring unbiased trial results. When such designs are not practical, BICR is not recommended as a general strategy for reducing bias. However, BICR may be useful as an auditing tool to assess the reliability of marginally positive results.
引用
收藏
页码:3791 / 3796
页数:6
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