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    Arch Neurol. 2010 Nov;67(11):1329-35. Epub 2010 Jul 12.

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

    Source

    Mellen Center for Multiple Sclerosis Treatment and Research, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH 44195, USA. rudickr@ccf.org

    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.

    PMID:
    20625068
    [PubMed - indexed for MEDLINE]
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