Latent Subgroup Analysis of a Randomized Clinical Trial through a Semiparametric Accelerated Failure Time Mixture Model

被引:33
作者
Altstein, L. [1 ]
Li, G. [2 ]
机构
[1] Novartis Inst Biomed Res, Cambridge, MA 02139 USA
[2] Univ Calif Los Angeles, Sch Publ Hlth, Dept Biostat, Los Angeles, CA 90095 USA
关键词
All-or-none noncompliance; BuckleyJames estimator; Clinical trials; Competing risks; EM algorithm; Nonproportional hazards model; Treatment efficacy; LINEAR-REGRESSION; CENSORED-DATA; NODE BIOPSY; NONCOMPLIANCE; INFERENCE; ESTIMATOR; COMPLIERS; EFFICACY; TESTS;
D O I
10.1111/j.1541-0420.2012.01818.x
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This article studies a semiparametric accelerated failure time mixture model for estimation of a biological treatment effect on a latent subgroup of interest with a time-to-event outcome in randomized clinical trials. Latency is induced because membership is observable in one arm of the trial and unidentified in the other. This method is useful in randomized clinical trials with all-or-none noncompliance when patients in the control arm have no access to active treatment and in, for example, oncology trials when a biopsy used to identify the latent subgroup is performed only on subjects randomized to active treatment. We derive a computational method to estimate model parameters by iterating between an expectation step and a weighted BuckleyJames optimization step. The bootstrap method is used for variance estimation, and the performance of our method is corroborated in simulation. We illustrate our method through an analysis of a multicenter selective lymphadenectomy trial for melanoma.
引用
收藏
页码:52 / 61
页数:10
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