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

Zhengjia Chen, Ying Yuan, Zheng Li, Michael Kutner, Taofeek Owonikoko, Walter J. Curran, Fadlo Khuri, Jeanne Kowalski

Research output: Contribution to journalArticlepeer-review

Abstract

To save valuable time and resources in new drug development, Phase I/II clinical trials with toxicity control and drug efficacy as dual primary endpoints have become increasingly popular. Escalation with over-dose control (the EWOC) is a Bayesian adaptive Phase I clinical trial design that can accurately estimate the maximum tolerated dose (MTD) level and control the probability of overdosing patients during the dose allocation phase. In this paper, we extend EWOC to Phase I/II clinical trials by controlling for under-dosing with a Gumbel Copula model to provide patients with at least minimum drug efficacy. We propose a utility function to measure the composite effect of toxicity and efficacy and select the optimal dose. To deal with the common issue that the efficacy endpoint often cannot be quickly ascertained, we employ Bayesian data augmentation to handle delayed efficacy and allow for flexible patient accrual without a waiting period. Extensive simulations demonstrate that the proposed new design not only provides better therapeutic effect by reducing the probability of treating patients at under-dose levels while protecting patients from being overdosed, but also improves trial efficiency and increases the accuracy of dose recommendation for subsequent clinical trials. We apply the proposed design to a Phase I/II solid tumor trial.

Original languageEnglish (US)
Pages (from-to)133-141
Number of pages9
JournalContemporary Clinical Trials
Volume43
DOIs
StatePublished - Jul 1 2015

Keywords

  • Bayesian data augmentation
  • Escalation with over-dose control
  • Escalation with under-dose control
  • Gumbel copula model
  • Phase I/II clinical trial

ASJC Scopus subject areas

  • Pharmacology (medical)

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