Dose escalation with overdose control using a quasi-continuous toxicity score in cancer Phase I clinical trials

Contemp Clin Trials. 2012 Sep;33(5):949-58. doi: 10.1016/j.cct.2012.04.007. Epub 2012 Apr 25.

Abstract

Escalation with overdose control (EWOC) is a Bayesian adaptive design for selecting dose levels in cancer Phase I clinical trials while controlling the posterior probability of exceeding the maximum tolerated dose (MTD). EWOC has been used by clinicians to design many cancer Phase I clinical trials, see e.g. [1-4]. However, this design treats the toxicity response as a binary indicator of dose limiting toxicity (DLT) and does not account for the number and specific grades of toxicities experienced by patients during the trial. Chen et al. (2010) proposed a novel toxicity score system to fully utilize all toxicity information using a normalized equivalent toxicity score (NETS). In this paper, we propose to incorporate NETS into EWOC using a quasi-Bernoulli likelihood approach to design cancer Phase I clinical trials. We call the design escalation with overdose control using normalized equivalent toxicity score (EWOC-NETS). Simulation results show that this design has good operating characteristics and improves the accuracy of MTD, trial efficiency, therapeutic effect, and overdose control relative to EWOC which is used as a representative of designs treating toxicity response as a binary indicator of DLT. We illustrate the performance of this design using real trial data in identifying the Phase II dose.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Algorithms*
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use*
  • Bayes Theorem
  • Clinical Trials, Phase I as Topic / methods*
  • Computer Simulation
  • Dose-Response Relationship, Drug
  • Drug Overdose*
  • Humans
  • Likelihood Functions
  • Maximum Tolerated Dose
  • Neoplasms / drug therapy*
  • Randomized Controlled Trials as Topic / methods*

Substances

  • Antineoplastic Agents