The Bayesian Time Machine: Accounting for temporal drift in multi-arm platform trials

贝叶斯概率 频数推理 平滑的 计算机科学 背景(考古学) 人口 可信区间 统计 贝叶斯推理 人工智能 医学 数学 古生物学 环境卫生 生物
作者
Benjamin R. Saville,Donald A. Berry,Nicholas Berry,Kert Viele,Scott Berry
出处
期刊:Clinical Trials [SAGE Publishing]
卷期号:19 (5): 490-501 被引量:63
标识
DOI:10.1177/17407745221112013
摘要

Background Multi-arm platform trials investigate multiple agents simultaneously, typically with staggered entry and exit of experimental treatment arms versus a shared control arm. In such settings, there is considerable debate whether to limit analyses for a treatment arm to concurrent randomized control subjects or to allow comparisons to both concurrent and non-concurrent (pooled) control subjects. The potential bias from temporal drift over time is at the core of this debate. Methods We propose time-adjusted analyses, including a “Bayesian Time Machine,” to model potential temporal drift in the entire study population, such that primary analyses can incorporate all randomized control subjects from the platform trial. We conduct a simulation study to assess performance relative to utilizing concurrent or pooled controls. Results In multi-arm platform trials with staggered entry, analyses adjusting for temporal drift (either Bayesian or frequentist) have superior estimation of treatment effects and favorable testing properties compared to analyses using either concurrent or pooled controls. The Bayesian Time Machine generally provides estimates with greater precision and smaller mean square error than alternative approaches, at the risk of small bias and small Type I error inflation. Conclusions The Bayesian Time Machine provides a compromise between bias and precision by smoothing estimates across time and leveraging all available data for the estimation of treatment effects. Prior distributions controlling the behavior of dynamic smoothing across time must be pre-specified and carefully calibrated to the unique context of each trial, appropriately accounting for the population, disease, and endpoints.
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