Testing of evaluation bias for progression free survival endpoint in oncology clinical trials

Stat Med. 2016 Sep 30;35(22):3923-32. doi: 10.1002/sim.6963. Epub 2016 Apr 18.

Abstract

Progression-free survival is an increasingly popular end point in oncology clinical trials. A complete blinded independent central review (BICR) is often required by regulators in an attempt to reduce the bias in progression-free survival (PFS) assessment. In this paper, we propose a new methodology that uses a sample-based BICR as an audit tool to decide whether a complete BICR is needed. More specifically, we propose a new index, the differential risk, to measure the reading discordance pattern, and develop a corresponding hypothesis testing procedure to decide whether the bias in local evaluation is acceptable. Simulation results demonstrate that our new index is sensitive to the change of discordance pattern; type I error is well controlled in the hypothesis testing procedure, and the calculated sample size provides the desired power. Copyright © 2016 John Wiley & Sons, Ltd.

Keywords: hypothesis test; independent review; progression free survival.

MeSH terms

  • Bias
  • Clinical Trials as Topic*
  • Disease-Free Survival
  • Endpoint Determination*
  • Humans
  • Medical Oncology
  • Neoplasms / therapy*
  • Sample Size