open access publication

Article, 2023

Confirmatory prediction-driven RCTs in comparative effectiveness settings for cancer treatment

BRITISH JOURNAL OF CANCER, ISSN 0007-0920, 0007-0920, Volume 128, 7, Pages 1278-1285, 10.1038/s41416-023-02144-x

Contributors

Brand, Adam 0000-0003-1300-5292 (Corresponding author) [1] Sachs, M. 0000-0002-1279-8676 [1] [2] Sjoelander, A. [1] Gabriel, Erin E. E. [1] [2]

Affiliations

  1. [1] Karolinska Inst, Dept Med Epidemiol & Biostat, Solna, Sweden
  2. [NORA names: Sweden; Europe, EU; Nordic; OECD];
  3. [2] Univ Copenhagen, Dept Publ Hlth Sect Biostat, Copenhagen, Denmark
  4. [NORA names: KU University of Copenhagen; University; Denmark; Europe, EU; Nordic; OECD]

Abstract

BackgroundMedical advances in the treatment of cancer have allowed the development of multiple approved treatments and prognostic and predictive biomarkers for many types of cancer. Identifying improved treatment strategies among approved treatment options, the study of which is termed comparative effectiveness, using predictive biomarkers is becoming more common. RCTs that incorporate predictive biomarkers into the study design, called prediction-driven RCTs, are needed to rigorously evaluate these treatment strategies. Although researched extensively in the experimental treatment setting, literature is lacking in providing guidance about prediction-driven RCTs in the comparative effectiveness setting.MethodsRealistic simulations with time-to-event endpoints are used to compare contrasts of clinical utility and provide examples of simulated prediction-driven RCTs in the comparative effectiveness setting.ResultsOur proposed contrast for clinical utility accurately estimates the true clinical utility in the comparative effectiveness setting while in some scenarios, the contrast used in current literature does not.DiscussionIt is important to properly define contrasts of interest according to the treatment setting. Realistic simulations should be used to choose and evaluate the RCT design(s) able to directly estimate that contrast. In the comparative effectiveness setting, our proposed contrast for clinical utility should be used.

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