Abstract
We propose a novel response‐adaptive randomization procedure for multi‐armed trials with continuous outcomes that are assumed to be normally distributed. Our proposed rule is non‐myopic, and oriented toward a patient benefit objective, yet maintains computational feasibility. We derive our response‐adaptive algorithm based on the Gittins index for the multi‐armed bandit problem, as a modification of the method first introduced in Villar et al. (Biometrics, 71, pp. 969‐978). The resulting procedure can be implemented under the assumption of both known or unknown variance. We illustrate the proposed procedure by simulations in the context of phase II cancer trials. Our results show that, in a multi‐armed setting, there are efficiency and patient benefit gains of using a response‐adaptive allocation procedure with a continuous endpoint instead of a binary one. These gains persist even if an anticipated low rate of missing data due to deaths, dropouts, or complete responses is imputed online through a procedure first introduced in this paper. Additionally, we discuss how there are response‐adaptive designs that outperform the traditional equal randomized design both in terms of efficiency and patient benefit measures in the multi‐armed trial context.
Highlights
Response‐adaptive randomization (RAR) has been widely developed ever since the idea was first suggested by Thompson (1933) (Hu and Rosenberger, 2006)
The RAR literature contains relatively few procedures for a continuous endpoint assumed to be normally distributed with unknown variance, fewer still that are defined for the multi‐armed case and none that are forward‐looking
We propose the first forward‐looking RAR algorithm applicable to this case which is oriented toward an optimality criterion with respect to patient benefit
Summary
A response‐adaptive randomization procedure for multi‐armed clinical trials with normally distributed outcomes. Funding information Engineering and Physical Sciences Research Council, Grant/Award Number: EP/H023151/1; Medical Research Council, Grant/Award Number: MC UU 00002/3
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