Literature DB >> 34085764

Bayesian single-arm phase II trial designs with time-to-event endpoints.

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.
© 2021 John Wiley & Sons Ltd.

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


  13 in total

1.  Monitoring event times in early phase clinical trials: some practical issues.

Authors:  Peter F Thall; Leiko H Wooten; Nizar M Tannir
Journal:  Clin Trials       Date:  2005       Impact factor: 2.486

2.  TOP: Time-to-Event Bayesian Optimal Phase II Trial Design for Cancer Immunotherapy.

Authors:  Ruitao Lin; Robert L Coleman; Ying Yuan
Journal:  J Natl Cancer Inst       Date:  2020-01-01       Impact factor: 13.506

3.  Bayesian enhancement two-stage design for single-arm phase II clinical trials with binary and time-to-event endpoints.

Authors:  Haolun Shi; Guosheng Yin
Journal:  Biometrics       Date:  2018-02-21       Impact factor: 2.571

4.  Two-stage optimal designs based on exact variance for a single-arm trial with survival endpoints.

Authors:  Guogen Shan
Journal:  J Biopharm Stat       Date:  2020-03-04       Impact factor: 1.051

5.  Bayesian decision theoretic two-stage design in phase II clinical trials with survival endpoint.

Authors:  Lili Zhao; Jeremy M G Taylor; Scott M Schuetze
Journal:  Stat Med       Date:  2012-02-23       Impact factor: 2.373

6.  MIDAS: a practical Bayesian design for platform trials with molecularly targeted agents.

Authors:  Ying Yuan; Beibei Guo; Mark Munsell; Karen Lu; Amir Jazaeri
Journal:  Stat Med       Date:  2016-04-25       Impact factor: 2.373

7.  Bayesian methods for setting sample sizes and choosing allocation ratios in phase II clinical trials with time-to-event endpoints.

Authors:  Amy Cotterill; John Whitehead
Journal:  Stat Med       Date:  2015-01-26       Impact factor: 2.373

8.  Two-stage phase II survival trial design.

Authors:  Jianrong Wu; Li Chen; Jing Wei; Heidi Weiss; Aman Chauhan
Journal:  Pharm Stat       Date:  2019-11-21       Impact factor: 1.234

9.  A proposed architecture and method of operation for improving the protection of privacy and confidentiality in disease registers.

Authors:  Tim Churches
Journal:  BMC Med Res Methodol       Date:  2003-01-06       Impact factor: 4.615

10.  A two-stage design for phase II trials with time-to-event endpoint using restricted follow-up.

Authors:  Lisa Belin; Yann De Rycke; Philippe Broët
Journal:  Contemp Clin Trials Commun       Date:  2017-10-01
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