Literature DB >> 22718676

Dose-finding designs: the role of convergence properties.

Assaf P Oron1, David Azriel, Peter D Hoff.   

Abstract

It is common for novel dose-finding designs to be presented without a study of their convergence properties. In this article we suggest that examination of convergence is a necessary quality check for dose-finding designs. We present a new convergence proof for a nonparametric family of methods called "interval designs," under certain conditions on the toxicity-frequency function F. We compare these conditions with the convergence conditions for the popular CRM one-parameter Phase I cancer design, via an innovative numerical sensitivity study generating a diverse sample of dose-toxicity scenarios. Only a small fraction of scenarios meet the Shen-O'Quigley convergence conditions for CRM. Conditions for "interval design" convergence are met more often, but still less than half the time. In the discussion, we illustrate how convergence properties and limitations help provide insight about small-sample behavior.

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Year:  2011        PMID: 22718676     DOI: 10.2202/1557-4679.1298

Source DB:  PubMed          Journal:  Int J Biostat        ISSN: 1557-4679            Impact factor:   0.968


  9 in total

1.  Bias induced by adaptive dose-finding designs.

Authors:  Nancy Flournoy; Assaf P Oron
Journal:  J Appl Stat       Date:  2019-08-01       Impact factor: 1.416

2.  Adaptive Clinical Trials: Overview of Early-Phase Designs and Challenges.

Authors:  Olga Marchenko; Valerii Fedorov; J Jack Lee; Christy Nolan; José Pinheiro
Journal:  Ther Innov Regul Sci       Date:  2013-11-26       Impact factor: 1.778

3.  A simulation-free approach to assessing the performance of the continual reassessment method.

Authors:  Thomas M Braun
Journal:  Stat Med       Date:  2020-09-16       Impact factor: 2.497

4.  Evaluating the effects of design parameters on the performances of phase I trial designs.

Authors:  Yaqian Zhu; Wei-Ting Hwang; Yimei Li
Journal:  Contemp Clin Trials Commun       Date:  2019-05-17

5.  An adaptive gBOIN design with shrinkage boundaries for phase I dose-finding trials.

Authors:  Rongji Mu; Zongliang Hu; Guoying Xu; Haitao Pan
Journal:  BMC Med Res Methodol       Date:  2021-12-13       Impact factor: 4.615

6.  Early phase clinical trials extension to guidelines for the content of statistical analysis plans.

Authors:  Victoria Homer; Christina Yap; Simon Bond; Jane Holmes; Deborah Stocken; Katrina Walker; Emily J Robinson; Graham Wheeler; Sarah Brown; Samantha Hinsley; Matthew Schipper; Christopher J Weir; Khadija Rantell; Thomas Prior; Ly-Mee Yu; John Kirkpatrick; Alun Bedding; Carrol Gamble; Piers Gaunt
Journal:  BMJ       Date:  2022-02-07

7.  A dose-finding design for phase I clinical trials based on Bayesian stochastic approximation.

Authors:  Jin Xu; Dapeng Zhang; Rongji Mu
Journal:  BMC Med Res Methodol       Date:  2022-10-01       Impact factor: 4.612

8.  Flexible, rule-based dose escalation: The cohort-sequence design.

Authors:  Shuang Li; Xian-Jin Xie; Daniel F Heitjan
Journal:  Contemp Clin Trials Commun       Date:  2020-02-09

Review 9.  A Brief Overview of Adaptive Designs for Phase I Cancer Trials.

Authors:  Anshul Saxena; Muni Rubens; Venkataraghavan Ramamoorthy; Zhenwei Zhang; Md Ashfaq Ahmed; Peter McGranaghan; Sankalp Das; Emir Veledar
Journal:  Cancers (Basel)       Date:  2022-03-18       Impact factor: 6.639

  9 in total

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