4.6 Article

Placebo Cohorts in Phase-3 MS Treatment Trials - Predictors for On-Trial Disease Activity 1990-2010 Based on a Meta-Analysis and Individual Case Data

Journal

PLOS ONE
Volume 7, Issue 11, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0050347

Keywords

-

Funding

  1. NEU2 consortium
  2. Federal Ministry of Education and Research (BMBF) (Forderkennzeichen) [0315610-0315620]
  3. Federal Ministry of Education and Research [01GI0904, 01GI0920]
  4. Mayo Clinic Rochester, European Union [215820]
  5. European Union [223865, LSHM-CT-2006-03759]
  6. Federal Ministry of Economics and Technology [KF0564001KF7]
  7. University of Oxford
  8. Technical University of Munich
  9. Hertie Foundation [1.01.1/07/015]
  10. Bavarian Research Foundation
  11. National Multiple Sclerosis Society (NMSS)
  12. Porticus Foundation [900.50578]
  13. University of Rochester, European Union [LSHM-CT-2004-503485]
  14. Sylvia Lawry Centre for Multiple Sclerosis Research

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Background: Annualized relapse rates (ARR) in the placebo cohorts of phase-3 randomized controlled trials (RCT) of new treatments for relapsing remitting multiple sclerosis (RRMS) have decreased substantially during the last two decades. The causes of these changes are not clear. We consider a better understanding of this phenomenon essential for valuing the effects of new drugs and by designing new trials. Objectives: To identify predictive factors of on-study ARR in early and recent MS trials. Methods: ARR, rate of relapse-free patients, trial start dates, baseline demographics, relapse definitions and the use of McDonald criteria were retrieved by literature research of the placebo cohorts from RRMS phase-3 trials. Predictors were estimated by univariate and multivariate regression analyses and random-effects meta-regression. In addition, regression models were calculated by the Sylvia Lawry Centre's (SLC), including individual case data from clinical trials performed until 2000. The most reliable meta-analytic results can be gained from pooled individual case data. In lack of this, random-effects meta-analyses are recommended. Results: Data from 12 published and one unpublished trial show a decrease of ARR from 1988 to 2012 (adjR(2) = 0.807, p<0.0001). Regression models identified McDonald criteria followed by baseline mean age and the pre-study relapse rate as predictors of the ARR. The pooled individual case data (n = 505) confirmed a decrease of ARR over time. The pre-study relapse rate was the best predictor for on-study relapses. Lacking individual case data after implementation of the McDonald criteria excludes a direct comparison concerning McDonald criteria. Conclusion: Pre-study relapse rate was the best predictor for on-study relapse rate but failed to explain the decrease of the ARR over time alone. Higher age at baseline and the implementation of McDonald criteria were associated as well with a lowered relapse rate in the random-effects meta-regression. These findings need further clarification based on individual case data.

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