Research Methods · Study Design

Using pilot data to size a two-arm randomized trial to find a nearly optimal personalized treatment strategy

Laber EB, Zhao YQ, Regh T, Davidian M, Tsiatis A, Zeng D, Song R, Kosorok MR, Stanford JB

Published April 15, 2016 Statistics in Medicine, 35(8), 1245-1256
DOI 10.1002/sim.6783 PMID 26506890 PMC PMC4777666

Abstract

A personalized treatment strategy formalizes evidence-based treatment selection by mapping patient information to a recommended treatment. Personalized treatment strategies can produce better patient outcomes while reducing cost and treatment burden. Thus, among clinical and intervention scientists, there is a growing interest in conducting randomized clinical trials when one of the primary aims is estimation of a personalized treatment strategy. However, at present, there are no appropriate sample size formulae to assist in the design of such a trial. Furthermore, because the sampling distribution of the estimated outcome under an estimated optimal treatment strategy can be highly sensitive to small perturbations in the underlying generative model, sample size calculations based on standard (uncorrected) asymptotic approximations or computer simulations may not be reliable. We offer a simple and robust method for powering a single stage, two-armed randomized clinical trial when the primary aim is estimating the optimal single stage personalized treatment strategy. The proposed method is based on inverting a plugin projection confidence interval and is thereby regular and robust to small perturbations of the underlying generative model. The proposed method requires elicitation of two clinically meaningful parameters from clinical scientists and uses data from a small pilot study to estimate nuisance parameters, which are not easily elicited. The method performs well in simulated experiments and is illustrated using data from a pilot study of time to conception and fertility awareness.

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By this author

Research Methods › Study Design › Randomized Controlled Trials
Eric B Laber, Ying Zhao, Marie Davidian, Anastasios Tsiatis, Joseph B Stanford, Donglin Zeng, Rui Song, Michael R Kosorok, Todd Regh
E Laber, Y Zhao, M Davidian, A Tsiatis, Joe Stanford, Joey Stanford, J Stanford, D Zeng, R Song, Mike Kosorok, M Kosorok, T Regh
PMID 26506890 26506890 DOI 10.1002/sim.6783 10.1002/sim.6783 Laber et al. 2016, Laber 2016