| Literature DB >> 34085764 |
Jianrong Wu1, Haitao Pan2, Chia-Wei Hsu2.
Abstract
For the cancer clinical trials with immunotherapy and molecularly targeted therapy, time-to-event endpoint is often a desired endpoint. In this paper, we present an event-driven approach for Bayesian one-stage and two-stage single-arm phase II trial designs. Two versions of Bayesian one-stage designs were proposed with executable algorithms and meanwhile, we also develop theoretical relationships between the frequentist and Bayesian designs. These findings help investigators who want to design a trial using Bayesian approach have an explicit understanding of how the frequentist properties can be achieved. Moreover, the proposed Bayesian designs using the exact posterior distributions accommodate the single-arm phase II trials with small sample sizes. We also proposed an optimal two-stage approach, which can be regarded as an extension of Simon's two-stage design with the time-to-event endpoint. Comprehensive simulations were conducted to explore the frequentist properties of the proposed Bayesian designs and an R package BayesDesign can be assessed via R CRAN for convenient use of the proposed methods.Entities:
Keywords: Bayesian design; phase II trial; proportional hazards; sample size calculation; time-to-event endpoint
Mesh:
Year: 2021 PMID: 34085764 PMCID: PMC9502026 DOI: 10.1002/pst.2143
Source DB: PubMed Journal: Pharm Stat ISSN: 1539-1604 Impact factor: 1.234