Literature DB >> 25545805

A randomized two-stage design for phase II clinical trials based on a Bayesian predictive approach.

Matteo Cellamare1, Valeria Sambucini.   

Abstract

The rate of failure in phase III oncology trials is surprisingly high, partly owing to inadequate phase II studies. Recently, the use of randomized designs in phase II is being increasingly recommended, to avoid the limits of studies that use a historical control. We propose a two-arm two-stage design based on a Bayesian predictive approach. The idea is to ensure a large probability, expressed in terms of the prior predictive probability of the data, of obtaining a substantial posterior evidence in favour of the experimental treatment, under the assumption that it is actually more effective than the standard agent. This design is a randomized version of the two-stage design that has been proposed for single-arm phase II trials by Sambucini. We examine the main features of our novel design as all the parameters involved vary and compare our approach with Jung's minimax and optimal designs. An illustrative example is also provided online as a supplementary material to this article.
Copyright © 2014 John Wiley & Sons, Ltd.

Keywords:  Bayesian predictive approach; analysis and design priors; phase II clinical trials; randomized trials; two-stage designs

Mesh:

Year:  2014        PMID: 25545805     DOI: 10.1002/sim.6396

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


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