Inference on treatment effects for targeted clinical trials under enrichment design

Jen-Pei Liu1, Jr-Rung Lin, Shein-Chung Chow

  • 1Division of Biometry, Department of Agronomy, National Taiwan University, Taipei, Taiwan. jpliu@ntu.edu.tw

Pharmaceutical Statistics
|January 31, 2009
PubMed

Insights

This study introduces a new method to accurately estimate targeted drug effectiveness in clinical trials, even with imperfect diagnostic tests. The approach ensures unbiased results for patients truly benefiting from the treatment.

Area of Science:

  • Biostatistics
  • Genomics
  • Clinical Trial Design

Background:

  • Human genome project enables molecular target identification for personalized medicine.
  • Targeted clinical trials evaluate individualized treatments but face diagnostic accuracy limitations.
  • Imperfect diagnostics can bias treatment effect estimates in targeted trials.

Purpose of the Study:

  • To develop a statistical method for unbiased estimation of targeted drug effects.
  • To address bias in targeted clinical trials caused by inaccurate diagnostic devices.
  • To provide reliable inference for patient populations with specific molecular targets.

Main Methods:

  • Utilized the Expectation-Maximization (EM) algorithm and bootstrap method.
  • Employed an enrichment design for targeted clinical trials.
  • Conducted simulation studies to assess estimator bias, variability, and testing procedure performance.

Main Results:

  • The proposed estimator demonstrated unbiasedness with adequate precision.
  • Confidence intervals achieved satisfactory coverage probability.
  • The testing procedure effectively controlled statistical size and exhibited sufficient power.

Conclusions:

  • The proposed statistical method accurately estimates targeted drug effects in patient populations with molecular targets.
  • The approach mitigates bias introduced by imperfect diagnostic devices in clinical trials.
  • Simulation and practical examples confirm the method's utility and reliability.

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