| Literature DB >> 30203592 |
Zhenzhen Xu1, Yongsoek Park2, Boguang Zhen1, Bin Zhu3.
Abstract
In some clinical settings such as the cancer immunotherapy trials, a treatment time-lag effect may be present and the lag duration possibly vary from subject to subject. An efficient study design and analysis procedure should not only take into account the time-lag effect but also consider the individual heterogeneity in the lag duration. In this paper, we present a Generalized Piecewise Weighted Logrank (GPW-Logrank) test, designed to account for the random time-lag effect while maximizing the study power with respect to the weights. Based on the proposed test, both analytic and numeric approaches are developed for the sample size and power calculation. Asymptotic properties are derived and finite sample efficiency is evaluated in simulations. Compared with the standard practice ignoring the delayed effect, the proposed design and analysis procedures are substantially more efficient when a random lag is expected; further, compared with the existing methods by Xu et al considering the fixed time-lag effect, the proposed approaches are significantly more robust when the lag model is misspecified. An R package (DelayedEffect.Design) is developed for implementation. Published 2018. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: cancer immunotherapy; clinical trial; nonproportional hazards assumption; random time-lag effect; sample size and power calculation; treatment time-lag effect
Mesh:
Year: 2018 PMID: 30203592 PMCID: PMC6279582 DOI: 10.1002/sim.7937
Source DB: PubMed Journal: Stat Med ISSN: 0277-6715 Impact factor: 2.373