关于贝叶斯顺序临床试验设计

Tianjian Zhou, Yuan Ji
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引用次数: 1

摘要

临床试验通常涉及顺序患者入组。在设计临床试验时,通常希望包括对积累的数据进行中期分析的规定,这些数据有可能提前停止试验。我们回顾了基于后验概率、后验预测概率和决策理论框架的贝叶斯顺序临床试验设计。一个相关的问题是贝叶斯序列设计是否需要为中期分析的规划进行调整。我们从三个角度回答这个问题:频率导向的角度,校准贝叶斯的角度,和主观贝叶斯的角度。我们还提供了新的见解的可能性原则,这是通常与统计推断和决策制定顺序临床试验。推导了一些理论结果,并进行了数值研究来说明和评估这些设计。
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On Bayesian Sequential Clinical Trial Designs
Clinical trials usually involve sequential patient entry. When designing a clinical trial, it is often desirable to include a provision for interim analyses of accumulating data with the potential for stopping the trial early. We review Bayesian sequential clinical trial designs based on posterior probabilities, posterior predictive probabilities, and decision-theoretic frameworks. A pertinent question is whether Bayesian sequential designs need to be adjusted for the planning of interim analyses. We answer this question from three perspectives: a frequentist-oriented perspective, a calibrated Bayesian perspective, and a subjective Bayesian perspective. We also provide new insights into the likelihood principle, which is commonly tied to statistical inference and decision making in sequential clinical trials. Some theoretical results are derived, and numerical studies are conducted to illustrate and assess these designs.
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