Literature DB >> 30101616

Revisiting isotonic phase I design in the era of model-assisted dose-finding.

Nolan A Wages1, Mark R Conaway1.   

Abstract

Background/aims In the conduct of phase I trials, the limited use of innovative model-based designs in practice has led to an introduction of a class of "model-assisted" designs with the aim of effectively balancing the trade-off between design simplicity and performance. Prior to the recent surge of these designs, methods that allocated patients to doses based on isotonic toxicity probability estimates were proposed. Like model-assisted methods, isotonic designs allow investigators to avoid difficulties associated with pre-trial parametric specifications of model-based designs. The aim of this work is to take a fresh look at an isotonic design in light of the current landscape of model-assisted methods. Methods The isotonic phase I method of Conaway, Dunbar, and Peddada was proposed in 2004 and has been regarded primarily as a design for dose-finding in drug combinations. It has largely been overlooked in the single-agent setting. Given its strong simulation performance in application to more complex dose-finding problems, such as drug combinations and patient heterogeneity, as well as the recent development of user-friendly software to accompany the method, we take a fresh look at this design and compare it to a current model-assisted method. We generated operating characteristics of the Conaway-Dunbar-Peddada method using a new web application developed for simulating and implementing the design and compared it to the recently proposed Keyboard design that is based on toxicity probability intervals. Results The Conaway-Dunbar-Peddada method has better performance in terms of accuracy of dose recommendation and safety in patient allocation in 17 of 20 scenarios considered. The Conaway-Dunbar-Peddada method also allocated fewer patients to doses above the maximum tolerated dose than the Keyboard method in many of scenarios studied. Overall, the performance of the Conaway-Dunbar-Peddada method is strong when compared to the Keyboard method, making it a viable simple alternative to the model-assisted methods developed in recent years. Conclusion The Conaway-Dunbar-Peddada method does not rely on the specification and fitting of a parametric model for the entire dose-toxicity curve to estimate toxicity probabilities as other model-based designs do. It relies on a similar set of pre-trial specifications to toxicity probability interval-based methods, yet unlike model-assisted methods, it is able to borrow information across all dose levels, increasing its efficiency. We hope this concise study of the Conaway-Dunbar-Peddada method, and the availability of user-friendly software, will augment its use in practice.

Entities:  

Keywords:  Dose-finding; isotonic regression; order-restricted inference; phase I

Mesh:

Year:  2018        PMID: 30101616      PMCID: PMC6133737          DOI: 10.1177/1740774518792258

Source DB:  PubMed          Journal:  Clin Trials        ISSN: 1740-7745            Impact factor:   2.486


  21 in total

1.  On the use of nonparametric curves in phase I trials with low toxicity tolerance.

Authors:  Ying Kuen Cheung
Journal:  Biometrics       Date:  2002-03       Impact factor: 2.571

2.  Isotonic designs for phase I trials in partially ordered groups.

Authors:  Mark Conaway
Journal:  Clin Trials       Date:  2017-08-04       Impact factor: 2.486

3.  Designs for single- or multiple-agent phase I trials.

Authors:  Mark R Conaway; Stephanie Dunbar; Shyamal D Peddada
Journal:  Biometrics       Date:  2004-09       Impact factor: 2.571

4.  Performance of toxicity probability interval based designs in contrast to the continual reassessment method.

Authors:  Bethany Jablonski Horton; Nolan A Wages; Mark R Conaway
Journal:  Stat Med       Date:  2016-07-19       Impact factor: 2.373

5.  Bayesian Optimal Interval Design: A Simple and Well-Performing Design for Phase I Oncology Trials.

Authors:  Ying Yuan; Kenneth R Hess; Susan G Hilsenbeck; Mark R Gilbert
Journal:  Clin Cancer Res       Date:  2016-07-12       Impact factor: 12.531

Review 6.  Practical designs for Phase I combination studies in oncology.

Authors:  Nolan A Wages; Anastasia Ivanova; Olga Marchenko
Journal:  J Biopharm Stat       Date:  2016       Impact factor: 1.051

7.  Keyboard: A Novel Bayesian Toxicity Probability Interval Design for Phase I Clinical Trials.

Authors:  Fangrong Yan; Sumithra J Mandrekar; Ying Yuan
Journal:  Clin Cancer Res       Date:  2017-05-25       Impact factor: 12.531

8.  A design for phase I trials in completely or partially ordered groups.

Authors:  Mark R Conaway
Journal:  Stat Med       Date:  2017-04-06       Impact factor: 2.373

9.  Uptake of novel statistical methods for early-phase clinical studies in the UK public sector.

Authors:  Thomas Jaki
Journal:  Clin Trials       Date:  2013-02-01       Impact factor: 2.486

Review 10.  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

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  2 in total

1.  Adaptive dose-finding based on safety and feasibility in early-phase clinical trials of adoptive cell immunotherapy.

Authors:  Nolan A Wages; Camilo E Fadul
Journal:  Clin Trials       Date:  2019-12-19       Impact factor: 2.486

Review 2.  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

  2 in total

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