Department of Biostatistics and Computational Biology, University of Rochester, Rochester, New York.
Biometrics. 2022 Dec;78(4):1503-1514. doi: 10.1111/biom.13504. Epub 2021 Jun 15.
An adaptive treatment length strategy is a sequential stage-wise treatment strategy where a subject's treatment begins at baseline and one chooses to stop or continue treatment at each stage provided the subject has been continuously treated. The effects of treatment are assumed to be cumulative and, therefore, the effect of treatment length on clinical endpoint, measured at the end of the study, is of primary scientific interest. At the same time, adverse treatment-terminating events may occur during the course of treatment that require treatment be stopped immediately. Because the presence of a treatment-terminating event may be strongly associated with the study outcome, the treatment-terminating event is informative. In observational studies, decisions to stop or continue treatment depend on covariate history that confounds the relationship between treatment length on outcome. We propose a new risk-set weighted estimator of the mean potential outcome under the condition that time-dependent covariates update at a set of common landmarks. We show that our proposed estimator is asymptotically linear given mild assumptions and correctly specified working models. Specifically, we study the theoretical properties of our estimator when the nuisance parameters are modeled using either parametric or semiparametric methods. The finite sample performance and theoretical results of the proposed estimator are evaluated through simulation studies and demonstrated by application to the Enhanced Suppression of the Platelet Receptor IIb/IIIa with Integrilin Therapy (ESPRIT) infusion trial data.
一种自适应治疗时长策略是一种序贯阶段式治疗策略,其中受试者的治疗从基线开始,如果受试者持续接受治疗,则在每个阶段选择停止或继续治疗。假设治疗效果是累积的,因此,治疗时长对研究结束时临床终点的影响是主要的科学关注点。同时,在治疗过程中可能会发生不良的治疗终止事件,需要立即停止治疗。由于治疗终止事件的存在可能与研究结果密切相关,因此该事件具有信息性。在观察性研究中,停止或继续治疗的决策取决于协变量历史,这会混淆治疗时长与结局之间的关系。我们提出了一种新的风险集加权估计量,用于在时变协变量在一组共同标记点更新的条件下估计潜在结果的平均值。我们证明,在假设和正确指定的工作模型下,我们提出的估计量是渐近线性的。具体而言,我们研究了当使用参数或半参数方法对干扰参数进行建模时,我们的估计量的理论性质。通过模拟研究评估了所提出的估计量的有限样本性能和理论结果,并通过对增强血小板受体 IIb/IIIa 抑制素治疗(ESPRIT)输注试验数据的应用进行了演示。