Phase I-II clinical trial design: a state-of-the-art paradigm for dose finding

Ann Oncol. 2018 Mar 1;29(3):694-699. doi: 10.1093/annonc/mdx795.

Abstract

Background: Conventional phase I algorithms for finding a phase-2 recommended dose (P2RD) based on toxicity alone is problematic because the maximum tolerated dose (MTD) is not necessarily the optimal dose with the most desirable risk-benefit trade-off. Moreover, the increasingly common practice of treating an expansion cohort at a chosen MTD has undesirable consequences that may not be obvious.

Patients and methods: We review the phase I-II paradigm and the EffTox design, which utilizes both efficacy and toxicity to choose optimal doses for successive patient cohorts and find the optimal P2RD. We conduct a computer simulation study to compare the performance of the EffTox design with the traditional 3 + 3 design and the continuous reassessment method.

Results: By accounting for the risk-benefit trade-off, the EffTox phase I-II design overcomes the limitations of conventional toxicity-based phase I designs. Numerical simulations show that the EffTox design has higher probabilities of identifying the optimal dose and treats more patients at the optimal dose.

Conclusions: Phase I-II designs, such as the EffTox design, provide a coherent and efficient approach to finding the optimal P2RD by explicitly accounting for risk-benefit trade-offs underlying medical decisions.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / adverse effects*
  • Clinical Trials, Phase I as Topic* / methods
  • Clinical Trials, Phase I as Topic* / standards
  • Clinical Trials, Phase II as Topic* / methods
  • Clinical Trials, Phase II as Topic* / standards
  • Computer Simulation*
  • Humans
  • Maximum Tolerated Dose
  • Research Design
  • Risk Assessment

Substances

  • Antineoplastic Agents