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AI 根据所提供的论文材料归类:摘要明确使用潜在结果、主层分层和随机试验研究因果效应识别及替代终点评价。

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关注这篇论文的作者
Zhichao Jiang
Peng Ding
Zhi Geng

利用多项试验识别主层因果效应并评价替代终点

研究问题
随机试验中由治疗后变量潜在结果定义的主层不可观测时,如何借助多项试验识别层内因果效应,并评价替代终点?
方法与思路
作者以跨试验主层因果效应同质性替代排除限制,讨论取消单调性后的局部识别必要条件,并用贝叶斯层级模型开展敏感性分析。
材料陈述的贡献
摘要给出取消单调性时至少三项试验的局部识别必要条件;在所用结肠癌试验中,作者报告三年无病生存满足所述替代终点评价准则。
阅读关注点
应核对同质性假设、主层定义及识别条件,特别区分至少三项试验的必要性与充分性,并检查替代终点结论的敏感性。
阅读边界
仅依据所给Crossref摘要;至少三项试验不是充分识别保证,应用结论依赖跨试验同质性等条件,不能推广到其他疾病或终点。

原文摘要

Summary Principal stratification is a causal framework to analyse randomized experiments with a post-treatment variable between the treatment and end point variables. Because the principal strata defined by the potential outcomes of the post-treatment variable are not observable, we generally cannot identify the causal effects within principal strata. Motivated by a real data set of phase III adjuvant colon cancer clinical trials, we propose approaches to identifying and estimating the principal causal effects via multiple trials. For the identifiability, we remove the commonly used exclusion restriction assumption by stipulating that the principal causal effects are homogeneous across these trials. To remove another commonly used monotonicity assumption, we give a necessary condition for the local identifiability, which requires at least three trials. Applying our approaches to the data from adjuvant colon cancer clinical trials, we find that the commonly used monotonicity assumption is untenable, and disease-free survival with 3-year follow-up is a valid surrogate end point for overall survival with 5-year follow-up, which satisfies both causal necessity and causal sufficiency. We also propose a sensitivity analysis approach based on Bayesian hierarchical models to investigate the effect of the deviation from the homogeneity assumption.

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