| Literature DB >> 26787557 |
Zhenzhen Xu1, Michael Proschan2, Shiowjen Lee1.
Abstract
Minimization, a dynamic allocation method, is gaining popularity especially in cancer clinical trials. Aiming to achieve balance on all important prognostic factors simultaneously, this procedure can lead to a substantial reduction in covariate imbalance compared with conventional randomization in small clinical trials. While minimization has generated enthusiasm, some controversy exists over the proper analysis of such a trial. Critics argue that standard testing methods that do not account for the dynamic allocation algorithm can lead to invalid statistical inference. Acknowledging this limitation, the International Conference on Harmonization E9 guideline suggests that 'the complexity of the logistics and potential impact on analyses be carefully evaluated when considering dynamic allocation'. In this article, we investigate the proper analysis approaches to inference in a minimization design for both continuous and time-to-event endpoints and evaluate the validity and power of these approaches under a variety of scenarios both theoretically and empirically. Published 2016. This article is a U.S. Government work and is in the public domain in the USA. Published 2016. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: analyze as you randomize; covariate adaptive randomization; dynamic allocation; minimization; permutation test; power; randomization; re-randomization test; temporal trend; validity
Mesh:
Year: 2016 PMID: 26787557 DOI: 10.1002/sim.6874
Source DB: PubMed Journal: Stat Med ISSN: 0277-6715 Impact factor: 2.373