Literature DB >> 34249223

A comparative study of Bayesian optimal interval (BOIN) design with interval 3+3 (i3+3) design for phase I oncology dose-finding trials.

Yanhong Zhou1, Ruobing Li2, Fangrong Yan3, J Jack Lee1, Ying Yuan1.   

Abstract

Bayesian optimal interval (BOIN) design is a model-assisted phase I dose-finding design to find the maximum tolerated dose (MTD). The hallmark of the BOIN design is its concise decision rule - making the decision of dose escalation and de-escalation by simply comparing the observed dose-limiting toxicity (DLT) rate at the current dose with a pair of optimal dose escalation and de-escalation boundaries. The interval 3+3 (i3+3) design is a recently proposed algorithm-based dose-finding design based on a similar decision rule with some modifications. The similarity in the appearance of the two designs has caused confusions among practitioners. In this article, we demystify the i3+3 design by elucidating its links with the BOIN design and compare their similarities and differences, as well as pros and cons. We perform comprehensive simulation studies to compare the operating characteristics of the two designs. Our results show that, compared to the algorithm-based i3+3 design, which are characterized by ad hoc and often scientifically and logically incoherent decision rules, the mode-assisted BOIN design is not only simpler, but also statistically more rigorous with better operating characteristics, thus providing a better design choice for phase I oncology trials.

Entities:  

Keywords:  Algorithm-based design; Dose finding; Model-assisted design; Phase I trials

Year:  2020        PMID: 34249223      PMCID: PMC8261789          DOI: 10.1080/19466315.2020.1811147

Source DB:  PubMed          Journal:  Stat Biopharm Res        ISSN: 1946-6315            Impact factor:   1.452


  29 in total

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Authors:  Y K Cheung; R Chappell
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6.  Cancer phase I clinical trials: efficient dose escalation with overdose control.

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7.  The accelerated biased coin up-and-down design in phase I trials.

Authors:  Mario Stylianou; Dean A Follmann
Journal:  J Biopharm Stat       Date:  2004-02       Impact factor: 1.051

Review 8.  Embracing model-based designs for dose-finding trials.

Authors:  Sharon B Love; Sarah Brown; Christopher J Weir; Chris Harbron; Christina Yap; Birgit Gaschler-Markefski; James Matcham; Louise Caffrey; Christopher McKevitt; Sally Clive; Charlie Craddock; James Spicer; Victoria Cornelius
Journal:  Br J Cancer       Date:  2017-06-29       Impact factor: 7.640

9.  A comprehensive comparison of the continual reassessment method to the standard 3 + 3 dose escalation scheme in Phase I dose-finding studies.

Authors:  Alexia Iasonos; Andrew S Wilton; Elyn R Riedel; Venkatraman E Seshan; David R Spriggs
Journal:  Clin Trials       Date:  2008       Impact factor: 2.486

10.  Overall success rate of a safe and efficacious drug: Results using six phase 1 designs, each followed by standard phase 2 and 3 designs.

Authors:  Amy S Ruppert; Abigail B Shoben
Journal:  Contemp Clin Trials Commun       Date:  2018-08-24
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