A 2-year observational study of patients with relapsing-remitting multiple sclerosis converting to glatiramer acetate from other disease-modifying therapies: the COPTIMIZE trial

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Tjalf Ziemssen - , Department of Neurology (Author)
  • Ovidiu A. Bajenaru - , Carol Davila University of Medicine and Pharmacy (Author)
  • Adriana Carrá - , Hospital Británico de Buenos Aires (Author)
  • Nina de Klippel - , Jessa Hospital (Author)
  • João C. de Sá - , Hospital de Santa Mari (Author)
  • Astrid Edland - , Central Hospital of Buskerud (Author)
  • Jette L. Frederiksen - , University of Copenhagen (Author)
  • Olivier Heinzlef - , Hopital Tenon (Author)
  • Klimentini E. Karageorgiou - , General Hospital of Athens (Author)
  • Anne Marie Landtblom - , Linköping University (Author)
  • Miguel A. Macías Islas - , Universidad de Guadalajara (Author)
  • Niall Tubridy - , University College Dublin (Author)
  • Yossi Gilgun-Sherki - , Teva Pharmaceutical Industries Ltd. (Author)

Abstract

Studies suggest that patients with relapsing-remitting multiple sclerosis (RRMS) who do not benefit from other disease-modifying treatments (DMTs) may benefit from converting to glatiramer acetate (GA). COPTIMIZE was a 24-month observational study designed to assess the disease course of patients converting to GA 20 mg daily from another DMT. Eligible patients had converted to GA and had received prior DMT for 3–6 months, depending on the reasons for conversion. Patients were assessed at baseline and at 6, 12, 18, and 24 months. In total, 672 patients from 148 centers worldwide were included in the analysis. Change of therapy to GA was prompted primarily by lack of efficacy (53.6 %) or intolerable adverse events (AEs; 44.8 %). Over a 24-month period, 72.7 % of patients were relapse free. Mean annual relapse rate decreased from 0.86 [95 % confidence interval (CI) 0.81–0.91] before the change to 0.32 (95 % CI 0.26–0.40; p < 0.0001) at last observation, while the progression of disability was halted, as the Kurtzke Expanded Disability Status Scale (EDSS) scores remained stable. Patients improved significantly (p < 0.05) on measures of fatigue, quality of life, depression, and cognition; mobility scores remained stable. The results indicate that changing RRMS patients to GA is associated with positive treatment outcomes.

Details

Original languageEnglish
Pages (from-to)2101-2111
Number of pages11
JournalJournal of neurology
Volume261
Issue number11
Publication statusPublished - Nov 2014
Peer-reviewedYes

External IDs

PubMed 25119836
ORCID /0000-0001-8799-8202/work/171553437

Keywords

ASJC Scopus subject areas

Keywords

  • Disease-modifying therapy, Glatiramer acetate, Multiple sclerosis, RRMS