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Through simulation studies, we show that RAR (both versions) allocates more participants to better treatments compared to equal randomization, while reducing potential covariate imbalances. We also show that dynamic allocation using mixed models for repeated measures yields a smaller allocation proportion variance while having a similar covariate imbalance as regression models. Additionally, covariate imbalance was smallest for methods using covariate-adjusted RAR (CARA) in scenarios with small sample sizes and covariate prevalence less than 0.3. Covariate imbalance did not differ between RAR and CARA in simulations with larger sample sizes and higher covariate prevalence. 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引用次数: 0
摘要
研究设计包括中期分析,以便修改试验设计。这些分析可能有助于决定样本大小、无效性和安全性。此外,这些分析还可以为治疗臂之间的潜在差异提供证据。贝叶斯反应自适应随机化(RAR)会调整分配比例,使较少的参与者被分配到较差的治疗方案中。然而,这些分配变化可能会带来协变量不平衡。我们讨论了贝叶斯 RAR 的两个版本(对二元协变量进行协变量调整和不进行协变量调整),适用于使用变化评分和重复测量进行分析的连续结果,同时考虑使用回归模型或混合模型进行中期分析建模。通过模拟研究,我们发现与平等随机化相比,RAR(两种版本)能将更多参与者分配到更好的治疗中,同时减少潜在的协变量不平衡。我们还表明,使用重复测量混合模型进行动态分配可获得较小的分配比例方差,同时具有与回归模型类似的协变量不平衡。此外,在样本量较小且协变量流行率小于 0.3 的情况下,使用协变量调整 RAR(CARA)的方法的协变量不平衡最小。在样本量较大、共变因素流行率较高的模拟中,RAR 和 CARA 的共变因素不平衡性没有差异。因此,我们建议在小型试点/探索性研究中采用 CARA 方法,以确定候选治疗方法,供进一步的确证研究使用。
Bayesian Response Adaptive Randomization for Randomized Clinical Trials With Continuous Outcomes: The Role of Covariate Adjustment.
Study designs incorporate interim analyses to allow for modifications to the trial design. These analyses may aid decisions regarding sample size, futility, and safety. Furthermore, they may provide evidence about potential differences between treatment arms. Bayesian response adaptive randomization (RAR) skews allocation proportions such that fewer participants are assigned to the inferior treatments. However, these allocation changes may introduce covariate imbalances. We discuss two versions of Bayesian RAR (with and without covariate adjustment for a binary covariate) for continuous outcomes analyzed using change scores and repeated measures, while considering either regression or mixed models for interim analysis modeling. Through simulation studies, we show that RAR (both versions) allocates more participants to better treatments compared to equal randomization, while reducing potential covariate imbalances. We also show that dynamic allocation using mixed models for repeated measures yields a smaller allocation proportion variance while having a similar covariate imbalance as regression models. Additionally, covariate imbalance was smallest for methods using covariate-adjusted RAR (CARA) in scenarios with small sample sizes and covariate prevalence less than 0.3. Covariate imbalance did not differ between RAR and CARA in simulations with larger sample sizes and higher covariate prevalence. We thus recommend a CARA approach for small pilot/exploratory studies for the identification of candidate treatments for further confirmatory studies.
期刊介绍:
Pharmaceutical Statistics is an industry-led initiative, tackling real problems in statistical applications. The Journal publishes papers that share experiences in the practical application of statistics within the pharmaceutical industry. It covers all aspects of pharmaceutical statistical applications from discovery, through pre-clinical development, clinical development, post-marketing surveillance, consumer health, production, epidemiology, and health economics.
The Journal is both international and multidisciplinary. It includes high quality practical papers, case studies and review papers.