Literature DB >> 24707327

BAYESIAN DATA AUGMENTATION DOSE FINDING WITH CONTINUAL REASSESSMENT METHOD AND DELAYED TOXICITY.

Suyu Liu1, Guosheng Yin2, Ying Yuan1.   

Abstract

A major practical impediment when implementing adaptive dose-finding designs is that the toxicity outcome used by the decision rules may not be observed shortly after the initiation of the treatment. To address this issue, we propose the data augmentation continual re-assessment method (DA-CRM) for dose finding. By naturally treating the unobserved toxicities as missing data, we show that such missing data are nonignorable in the sense that the missingness depends on the unobserved outcomes. The Bayesian data augmentation approach is used to sample both the missing data and model parameters from their posterior full conditional distributions. We evaluate the performance of the DA-CRM through extensive simulation studies, and also compare it with other existing methods. The results show that the proposed design satisfactorily resolves the issues related to late-onset toxicities and possesses desirable operating characteristics: treating patients more safely, and also selecting the maximum tolerated dose with a higher probability. The new DA-CRM is illustrated with two phase I cancer clinical trials.

Entities:  

Keywords:  Bayesian adaptive design; Late-onset toxicity; Nonignorable missing data; Phase I clinical trial

Year:  2013        PMID: 24707327      PMCID: PMC3972824          DOI: 10.1214/13-AOAS661

Source DB:  PubMed          Journal:  Ann Appl Stat        ISSN: 1932-6157            Impact factor:   2.083


  18 in total

1.  An extension of the continual reassessment method using decision theory.

Authors:  Denis Heng-Yan Leung; You-Gan Wang
Journal:  Stat Med       Date:  2002-01-15       Impact factor: 2.373

2.  Posterior maximization and averaging for Bayesian working model choice in the continual reassessment method.

Authors:  T Daimon; S Zohar; J O'Quigley
Journal:  Stat Med       Date:  2011-02-24       Impact factor: 2.373

3.  Using the time-to-event continual reassessment method in the presence of partial orders.

Authors:  Nolan A Wages; Mark R Conaway; John O'Quigley
Journal:  Stat Med       Date:  2012-07-17       Impact factor: 2.373

4.  Phase I trials of molecularly targeted agents: should we pay more attention to late toxicities?

Authors:  Sophie Postel-Vinay; Carlos Gomez-Roca; L Rhoda Molife; Bhavesh Anghan; Antonin Levy; Ian Judson; Johann De Bono; Jean-Charles Soria; Stan Kaye; Xavier Paoletti
Journal:  J Clin Oncol       Date:  2011-03-28       Impact factor: 44.544

5.  Some practical improvements in the continual reassessment method for phase I studies.

Authors:  S N Goodman; M L Zahurak; S Piantadosi
Journal:  Stat Med       Date:  1995-06-15       Impact factor: 2.373

6.  Sequential designs for phase I clinical trials with late-onset toxicities.

Authors:  Y K Cheung; R Chappell
Journal:  Biometrics       Date:  2000-12       Impact factor: 2.571

7.  Phase I trial using a time-to-event continual reassessment strategy for dose escalation of cisplatin combined with gemcitabine and radiation therapy in pancreatic cancer.

Authors:  Jeffrey H Muler; Cornelius J McGinn; Daniel Normolle; Theodore Lawrence; Diane Brown; Gwen Hejna; Mark M Zalupski
Journal:  J Clin Oncol       Date:  2003-12-09       Impact factor: 44.544

Review 8.  Late effects of radiation therapy on the gastrointestinal tract.

Authors:  L R Coia; R J Myerson; J E Tepper
Journal:  Int J Radiat Oncol Biol Phys       Date:  1995-03-30       Impact factor: 7.038

9.  Phase I study of oxaliplatin, full-dose gemcitabine, and concurrent radiation therapy in pancreatic cancer.

Authors:  Sameer P Desai; Edgar Ben-Josef; Daniel P Normolle; Isaac R Francis; Joel K Greenson; Diane M Simeone; Alfred E Chang; Lisa M Colletti; Theodore S Lawrence; Mark M Zalupski
Journal:  J Clin Oncol       Date:  2007-10-10       Impact factor: 44.544

10.  Continual reassessment method for ordered groups.

Authors:  John O'Quigley; Xavier Paoletti
Journal:  Biometrics       Date:  2003-06       Impact factor: 2.571

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  23 in total

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

3.  A practical Bayesian design to identify the maximum tolerated dose contour for drug combination trials.

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Journal:  Stat Med       Date:  2016-08-31       Impact factor: 2.373

Review 4.  Model-Assisted Designs for Early-Phase Clinical Trials: Simplicity Meets Superiority.

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5.  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

6.  Dose escalation with over-dose and under-dose controls in Phase I/II clinical trials.

Authors:  Zhengjia Chen; Ying Yuan; Zheng Li; Michael Kutner; Taofeek Owonikoko; Walter J Curran; Fadlo Khuri; Jeanne Kowalski
Journal:  Contemp Clin Trials       Date:  2015-05-24       Impact factor: 2.226

7.  A nonparametric Bayesian method for dose finding in drug combinations cancer trials.

Authors:  Zahra S Razaee; Galen Cook-Wiens; Mourad Tighiouart
Journal:  Stat Med       Date:  2022-01-25       Impact factor: 2.373

8.  Time-to-event model-assisted designs for dose-finding trials with delayed toxicity.

Authors:  Ruitao Lin; Ying Yuan
Journal:  Biostatistics       Date:  2020-10-01       Impact factor: 5.899

9.  A Phase I-II Basket Trial Design to Optimize Dose-Schedule Regimes Based on Delayed Outcomes.

Authors:  Ruitao Lin; Peter F Thall; Ying Yuan
Journal:  Bayesian Anal       Date:  2020-03-28       Impact factor: 3.728

10.  Glofitamab, a Novel, Bivalent CD20-Targeting T-Cell-Engaging Bispecific Antibody, Induces Durable Complete Remissions in Relapsed or Refractory B-Cell Lymphoma: A Phase I Trial.

Authors:  Martin Hutchings; Franck Morschhauser; Gloria Iacoboni; Carmelo Carlo-Stella; Fritz C Offner; Anna Sureda; Gilles Salles; Joaquín Martínez-Lopez; Michael Crump; Denise N Thomas; Peter N Morcos; Cristiano Ferlini; Ann-Marie E Bröske; Anton Belousov; Marina Bacac; Natalie Dimier; David J Carlile; Linda Lundberg; David Perez-Callejo; Pablo Umaña; Tom Moore; Martin Weisser; Michael J Dickinson
Journal:  J Clin Oncol       Date:  2021-03-19       Impact factor: 50.717

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