Randomized Phase II Trials: A Long-Term Investment With Promising Returns

J Natl Cancer Inst. 2011 Jul 20;103(14):1093-100. doi: 10.1093/jnci/djr218. Epub 2011 Jun 27.

Abstract

Given the multitude of novel anticancer drugs and the limited resources available to study them, phase II trials should identify drugs with the highest probability of succeeding in subsequent phase III trials. Currently, single-arm phase II trial results are interpreted relative to historical control subjects, introducing selection bias and confounding that may limit the validity of the conclusions. The rate of success (defined as a statistically significant difference between arms) in phase III oncology trials is only 40%, suggesting that current phase II trials are insufficiently informative. However, simulation studies suggest that randomized phase II trials would have lower error rates and greater predictive power for phase III results. Randomized phase II trials may also be more informative than single-arm phase II trials because of the hypotheses being tested, the variety of possible endpoints, and the opportunities for biomarker discovery. There are a wide variety of randomized phase II designs that can be used, including the randomized discontinuation design, the delayed-start design, adaptive (Bayesian) designs, selection designs, and phase II/III designs. The barriers to widespread adoption of randomized phase II trials include time to completion, sample size considerations, and ethical concerns, but none are insurmountable. We conclude that randomized phase II trials are a worthy investment considering finite patient and financial resources and should be the rule rather than the exception for evaluating novel therapies in oncology.

Publication types

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

MeSH terms

  • Antineoplastic Agents* / therapeutic use
  • Chemotherapy, Adjuvant
  • Clinical Trials, Phase II as Topic* / methods
  • Clinical Trials, Phase II as Topic* / standards
  • Clinical Trials, Phase III as Topic
  • Confounding Factors, Epidemiologic
  • Endpoint Determination*
  • Evidence-Based Medicine
  • Health Resources* / statistics & numerical data
  • Humans
  • Life Expectancy
  • Molecular Targeted Therapy / methods
  • Molecular Targeted Therapy / standards
  • Molecular Targeted Therapy / trends
  • Patient Selection*
  • Randomized Controlled Trials as Topic* / methods
  • Randomized Controlled Trials as Topic* / statistics & numerical data
  • Reproducibility of Results*
  • Research Design* / standards
  • Research Design* / trends
  • Sample Size
  • Selection Bias
  • Time Factors
  • Treatment Failure

Substances

  • Antineoplastic Agents