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Disability progression in relapse-free multiple sclerosis patients on fingolimod versus interferon-beta/glatiramer acetate.

AbstractBACKGROUND:
Disability progression independent of relapses (PIRA) has been described as a frequent phenomenon in relapsing-remitting multiple sclerosis (RRMS).
OBJECTIVE:
To compare the occurrence of disability progression in relapse-free RRMS patients on interferon-beta/glatiramer acetate (IFN/GA) versus fingolimod.
METHODS:
This study is based on data from the Swiss association for joint tasks of health insurers. Time to relapse and 12-month confirmed disability progression were compared between treatment groups using multivariable Cox regression analysis with confounder adjustment. Inverse-probability weighting was applied to correct for the bias that patients on fingolimod have a higher chance to remain relapse-free than patients on IFN/GA.
RESULTS:
We included 1640 patients (64% IFN/GA, 36% fingolimod, median total follow-up time = 4-5 years). Disease-modifying treatment (DMT) groups were well balanced with regard to potential confounders. Disability progression was observed in 155 patients (8.8%) on IFN/GA and 51 (7.6%) on fingolimod, of which 44 and 23 were relapse-free during the initial DMT, respectively. Adjusted standard regression analysis on all patients indicated that those on fingolimod experience less frequently disability progression compared with IFN/GA (hazard ratio = 0.53 (95% confidence interval = 0.37-0.76)). After bias correction, this was also true for patients without relapses (hazard ratio=0.56 (95% confidence interval = 0.32-0.98).
CONCLUSION:
Our analysis indicates that fingolimod is superior to IFN/GA in preventing disability progression in both relapsing and relapse-free, young, newly diagnosed RRMS patients.
AuthorsViktor von Wyl, Pascal Benkert, André Moser, Johannes Lorscheider, Bernhard Décard, Peter Hänni, Carmen Lienert, Jens Kuhle, Tobias Derfuss, Ludwig Kappos, Özgür Yaldizli
JournalMultiple sclerosis (Houndmills, Basingstoke, England) (Mult Scler) Vol. 27 Issue 3 Pg. 439-448 (03 2021) ISSN: 1477-0970 [Electronic] England
PMID32463336 (Publication Type: Journal Article)
Chemical References
  • Immunosuppressive Agents
  • Glatiramer Acetate
  • Interferon-beta
  • Fingolimod Hydrochloride
Topics
  • Fingolimod Hydrochloride (therapeutic use)
  • Glatiramer Acetate (therapeutic use)
  • Humans
  • Immunosuppressive Agents
  • Interferon-beta
  • Multiple Sclerosis
  • Multiple Sclerosis, Relapsing-Remitting (drug therapy)
  • Recurrence

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