Disability progression in a clinical trial of relapsing-remitting multiple sclerosis: eight-year follow-up

Arch Neurol. 2010 Nov;67(11):1329-35. doi: 10.1001/archneurol.2010.150. Epub 2010 Jul 12.

Abstract

Objective: To investigate the value of Expanded Disability Status Scale (EDSS) worsening sustained for at least 6 months and other parameters as predictors for disability status.

Design: Retrospective analysis of the Multiple Sclerosis Collaborative Research Group study data.

Setting: The intramuscular interferon beta-1a pivotal trial was a double-blind, placebo-controlled phase 3 study.

Participants: Patients with relapsing-remitting multiple sclerosis who received at least 2 years of treatment and completed an EDSS evaluation 8 years postrandomization.

Intervention: Thirty micrograms of intramuscular interferon beta-1a or placebo once weekly during the 2-year clinical trial.

Main outcome measures: Positive predictive values for 6-month sustained progression during 2 years were calculated to determine the ability to predict disability status at 8 years. A multivariate logistic regression model was used to assess the relationship between predictors and EDSS milestones at follow-up.

Results: Forty-five patients had sustained 6-month EDSS progression during the clinical trial and 115 did not. Progression during the trial was the strongest predictor of reaching EDSS milestones at the follow-up visit, 8 years after randomization. Other independent predictors were treatment arm assignment and baseline EDSS score.

Conclusion: In this phase 3 clinical trial of intramuscular interferon beta-1a, compared with effects of treatment, baseline EDSS score, and number of relapses during the study, worsening of 1 point or more on EDSS from baseline lasting 6 months was the strongest predictor of clinically significant disability 8 years after randomization into the clinical trial.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial

MeSH terms

  • Disability Evaluation*
  • Disease Progression*
  • Double-Blind Method
  • Follow-Up Studies
  • Humans
  • Immunologic Factors / therapeutic use
  • Injections, Intramuscular
  • Interferon-beta / therapeutic use*
  • Logistic Models
  • Multiple Sclerosis, Relapsing-Remitting / drug therapy*
  • Predictive Value of Tests
  • Treatment Outcome

Substances

  • Immunologic Factors
  • Interferon-beta