ESTIMATING THE AVERAGE TREATMENT EFFECT IN RANDOMIZED CLINICAL TRIALS WITH ALL-OR-NONE COMPLIANCE

被引:2
作者
Zhang, Zhiwei [1 ]
Hu, Zonghui [2 ]
Follmann, Dean [2 ]
Nie, Lei [3 ]
机构
[1] NCI, Div Canc Treatment & Diag, Bethesda, MD 20892 USA
[2] Natl Inst Allergy & Infect Dis, Div Clin Res, Rockville, MD USA
[3] FDA, Ctr Drug Evaluat & Res, Silver Spring, MD USA
关键词
Complier-average treatment effect; effect modification; instrumental variable; non-compliance; principal stratification; unmeasured confounding; DOUBLY ROBUST ESTIMATION; CAUSAL INFERENCE; MORTALITY; MODELS;
D O I
10.1214/22-AOAS1627
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
Noncompliance is a common intercurrent event in randomized clini-cal trials that raises important questions about analytical objectives and ap-proaches. Motivated by the Multiple Risk Factor Intervention Trial (MRFIT), we consider how to estimate the average treatment effect (ATE) in random-ized trials with all-or-none compliance. Confounding is a major challenge in estimating the ATE, and conventional methods for confounding adjustment typically require the assumption of no unmeasured confounders which may be difficult to justify. Using randomized treatment assignment as an instru-mental variable, the ATE can be identified in the presence of unmeasured confounders under suitable assumptions, including an assumption that limits the effect-modifying activities of unmeasured confounders. We describe and compare several estimation methods based on different modeling assump-tions. Some of these methods are able to incorporate information from auxil-iary covariates for improved efficiency without introducing bias. The different methods are compared in a simulation study and applied to the MRFIT.
引用
收藏
页码:294 / 312
页数:19
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