Semiparametric regression analysis for composite endpoints subject to componentwise censoring

被引:7
|
作者
Diao, Guoqing [1 ]
Zeng, Donglin [2 ]
Ke, Chunlei [3 ]
Ma, Haijun [3 ]
Jiang, Qi [3 ]
Ibrahim, Joseph G. [2 ]
机构
[1] George Mason Univ, Dept Stat, 4400 Univ Dr, Fairfax, VA 22030 USA
[2] Univ N Carolina, Dept Biostat, CB 7420, Chapel Hill, NC 27599 USA
[3] Amgen Inc, One Amgen Ctr Dr, Thousand Oaks, CA 91320 USA
关键词
Composite endpoint; Hazard ratio; Progression-free survival; Semiparametric model; PROGRESSION-FREE SURVIVAL; MODELS;
D O I
10.1093/biomet/asy013
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Composite endpoints with censored data are commonly used as study outcomes in clinical trials. For example, progression-free survival is a widely used composite endpoint, with disease progression and death as the two components. Progression-free survival time is often defined as the time from randomization to the earlier occurrence of disease progression or death from any cause. The censoring times of the two components could be different for patients not experiencing the endpoint event. Conventional approaches, such as taking the minimum of the censoring times of the two components as the censoring time for progression-free survival time, may suffer from efficiency loss and could produce biased estimates of the treatment effect. We propose a new likelihood-based approach that decomposes the endpoints and models both the progression-free survival time and the time from disease progression to death. The censoring times for different components are distinguished. The approach makes full use of available information and provides a direct and improved estimate of the treatment effect on progression-free survival time. Simulations demonstrate that the proposed method outperforms several other approaches and is robust against various model misspecifications. An application to a prostate cancer clinical trial is provided.
引用
收藏
页码:403 / 418
页数:16
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