A Multi-state Model for Designing Clinical Trials for Testing Overall Survival Allowing for Crossover after Progression.

TitleA Multi-state Model for Designing Clinical Trials for Testing Overall Survival Allowing for Crossover after Progression.
Publication TypeJournal Article
Year of Publication2016
AuthorsXia, Fang, Stephen L. George, and Xiaofei Wang
JournalStat Biopharm Res
Volume8
Issue1
Pagination12-21
Date Published2016
ISSN1946-6315
Abstract

In designing a clinical trial for comparing two or more treatments with respect to overall survival (OS), a proportional hazards assumption is commonly made. However, in many cancer clinical trials, patients pass through various disease states prior to death and because of this may receive treatments other than originally assigned. For example, patients may crossover from the control treatment to the experimental treatment at progression. Even without crossover, the survival pattern after progression may be very different than the pattern prior to progression. The proportional hazards assumption will not hold in these situations and the design power calculated on this assumption will not be correct. In this paper we describe a simple and intuitive multi-state model allowing for progression, death before progression, post-progression survival and crossover after progression and apply this model to the design of clinical trials for comparing the OS of two treatments. For given values of the parameters of the multi-state model, we simulate the required number of deaths to achieve a specified power and the distribution of time required to achieve the requisite number of deaths. The results may be quite different from those derived using the usual PH assumption.

DOI10.1080/19466315.2015.1093539
Alternate JournalStat Biopharm Res
Original PublicationA multi-state model for designing clinical trials for testing overall survival allowing for crossover after progression.
PubMed ID27239255
PubMed Central IDPMC4879617
Grant ListP01 CA142538 / CA / NCI NIH HHS / United States