随机化推断在早期疫苗试验中揭示个体治疗效果的作用。

Zhe Chen, Xinran Li, Bo Zhang
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引用次数: 0

摘要

在早期疫苗试验中,当估计一种治疗方案对安慰剂或另一种治疗方案的因果效应时,随机化推断是一种强有力的工具。基于随机化的推断通常侧重于检验费雪的 "对任何参与者均无治疗效果 "的尖锐零假设或奈曼的 "无样本平均治疗效果 "的弱零假设。最近,很多人都在探索对治疗效果曲线的其他总结(例如治疗效果分布函数的量值)进行精确的随机化推断。在本文中,我们系统地回顾了对个体治疗效果(ITEs)的量化值进行基于随机化的精确推断的方法,并将一些结果扩展到一种特殊情况,即天真的参与者预计不会表现出对高度特异性终点的反应。这些方法适用于完全随机试验、分层完全随机试验,以及对可能来自不同试验的两个非随机臂进行比较的匹配研究。我们在模拟研究中使用合成数据评估了这些方法的实用性。最后,我们将这些方法应用于 HIV 疫苗试验网络研究 086(HVTN 086)和 HVTN 205,并展示了这些方法的广泛应用场景。复制本文所有分析的 R 代码可在第一作者的 GitHub 页面 https://github.com/Zhe-Chen-1999/ITE-Inference 找到。
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The role of randomization inference in unraveling individual treatment effects in early phase vaccine trials.

Randomization inference is a powerful tool in early phase vaccine trials when estimating the causal effect of a regimen against a placebo or another regimen. Randomization-based inference often focuses on testing either Fisher's sharp null hypothesis of no treatment effect for any participant or Neyman's weak null hypothesis of no sample average treatment effect. Many recent efforts have explored conducting exact randomization-based inference for other summaries of the treatment effect profile, for instance, quantiles of the treatment effect distribution function. In this article, we systematically review methods that conduct exact, randomization-based inference for quantiles of individual treatment effects (ITEs) and extend some results to a special case where naïve participants are expected not to exhibit responses to highly specific endpoints. These methods are suitable for completely randomized trials, stratified completely randomized trials, and a matched study comparing two non-randomized arms from possibly different trials. We evaluate the usefulness of these methods using synthetic data in simulation studies. Finally, we apply these methods to HIV Vaccine Trials Network Study 086 (HVTN 086) and HVTN 205 and showcase a wide range of application scenarios of the methods. R code that replicates all analyses in this article can be found in first author's GitHub page at https://github.com/Zhe-Chen-1999/ITE-Inference.

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Study design approaches for future active-controlled HIV prevention trials. The role of randomization inference in unraveling individual treatment effects in early phase vaccine trials. Nonlinear mixed-effects models for HIV viral load trajectories before and after antiretroviral therapy interruption, incorporating left censoring. Estimation and interpretation of vaccine efficacy in COVID-19 randomized clinical trials Sample size calculation for active-arm trial with counterfactual incidence based on recency assay.
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