4.6 Article

Improved stratification of ALS clinical trials using predicted survival

Journal

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY
Volume 5, Issue 4, Pages 474-485

Publisher

WILEY
DOI: 10.1002/acn3.550

Keywords

clinical trial stratification; trial methodology predictive analytics

Funding

  1. Voyager Therapeutics, Inc.
  2. Amyotrophic Lateral Sclerosis Association [17-LGCA-333]

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IntroductionIn small trials, randomization can fail, leading to differences in patient characteristics across treatment arms, a risk that can be reduced by stratifying using key confounders. In ALS trials, riluzole use (RU) and bulbar onset (BO) have been used for stratification. We hypothesized that randomization could be improved by using a multifactorial prognostic score of predicted survival as a single stratifier. MethodsWe defined a randomization failure as a significant difference between treatment arms on a characteristic. We compared randomization failure rates when stratifying for RU and BO (traditional stratification) to failure rates when stratifying for predicted survival using a predictive algorithm. We simulated virtual trials using the PRO-ACT database without application of a treatment effect to assess balance between cohorts. We performed 100 randomizations using each stratification method - traditional and algorithmic. We applied these stratification schemes to a randomization simulation with a treatment effect using survival as the endpoint and evaluated sample size and power. ResultsStratification by predicted survival met with fewer failures than traditional stratification. Stratifying predicted survival into tertiles performed best. Stratification by predicted survival was validated with an external dataset, the placebo arm from the BENEFIT-ALS trial. Importantly, we demonstrated a substantial decrease in sample size required to reach statistical power. ConclusionsStratifying randomization based on predicted survival using a machine learning algorithm is more likely to maintain balance between trial arms than traditional stratification methods. The methodology described here can translate to smaller, more efficient clinical trials for numerous neurological diseases.

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