Gilbert Peter B, Peng James, Han Larry, Lange Theis, Lu Yun, Nie Lei, Shih Mei-Chiung, Waddy Salina P, Wiley Ken, Yann Margot, Zafari Zafar, Ghosh Debashis, Follmann Dean, Juraska Michal, Díaz Iván
Vaccine and Infectious Disease and Public Health Sciences Divisions, Fred Hutchinson Cancer Center, 1100 Fairview AVE N PO Box 19024, Seattle, WA 98109, United States.
Department of Biostatistics, University of Washington, 3980 15th Avenue NE, Box 351617, Seattle, WA 98195, United States.
Biostatistics. 2024 Dec 31;26(1). doi: 10.1093/biostatistics/kxaf018.
For many rare diseases with no approved preventive interventions, promising interventions exist. However, it has proven difficult to conduct a pivotal phase 3 trial that could provide direct evidence demonstrating a beneficial effect of the intervention on the target disease outcome. When a promising putative surrogate endpoint(s) for the target outcome is available, surrogate-based provisional approval of an intervention may be pursued. Following the general Causal Roadmap rubric, we describe a surrogate endpoint-based provisional approval causal roadmap. Based on an observational study data set and a phase 3 randomized trial data set, this roadmap defines an approach to analyze the combined data set to draw a conservative inference about the treatment effect (TE) on the target outcome in the phase 3 study population. The observational study enrolls untreated individuals and collects baseline covariates, surrogate endpoints, and the target outcome, and is used to estimate the surrogate index-the regression of the target outcome on the surrogate endpoints and baseline covariates. The phase 3 trial randomizes participants to treated vs. untreated and collects the same data but is much smaller and hence very underpowered to directly assess TE, such that inference on TE is based on the surrogate index. This inference is made conservative by specifying 2 bias functions: one that expresses an imperfection of the surrogate index as a surrogate endpoint in the phase 3 study, and the other that expresses imperfect transport of the surrogate index in the untreated from the observational to the phase 3 study. Plug-in and nonparametric efficient one-step estimators of TE, with inferential procedures, are developed. The finite-sample performance of the estimators is evaluated in simulation studies. The causal roadmap is motivated by and illustrated with contemporary Group B Streptococcus vaccine development.
对于许多尚无获批预防干预措施的罕见病,其实存在有前景的干预措施。然而,事实证明开展一项关键的3期试验很困难,该试验本可提供直接证据,证明干预措施对目标疾病结局具有有益效果。当有针对目标结局的有前景的假定替代终点可用时,可寻求基于替代终点的干预措施临时批准。遵循一般的因果路线图规则,我们描述了一种基于替代终点的临时批准因果路线图。基于一项观察性研究数据集和一项3期随机试验数据集,该路线图定义了一种分析合并数据集的方法,以便在3期研究人群中对目标结局的治疗效果(TE)得出保守推断。观察性研究纳入未接受治疗的个体,收集基线协变量、替代终点和目标结局,并用于估计替代指数——目标结局关于替代终点和基线协变量的回归。3期试验将参与者随机分为治疗组和未治疗组,并收集相同的数据,但规模要小得多,因此直接评估TE的效能非常低,以至于对TE的推断基于替代指数。通过指定两个偏差函数使这种推断更加保守:一个偏差函数表示替代指数作为3期研究中的替代终点存在缺陷,另一个偏差函数表示未治疗组中替代指数从观察性研究到3期研究的传递存在缺陷。开发了带有推断程序的TE的插件式和非参数有效一步估计器。在模拟研究中评估了估计器的有限样本性能。因果路线图的灵感来自当代B族链球菌疫苗的研发,并以其为例进行说明。