Disease-modifying therapies were most effective if started within 3 years of diagnosis in a registry study.
Identifying the long-term impact of a delay in treatment has always been a major question in the multiple sclerosis (MS) field. To shed light on the problem, researchers identified 906 patients diagnosed with MS from 2001 through 2007 who previously participated in a registry to observe MS outcomes. Of these patients, 708 had received a total of 1484 immunomodulatory treatments; 69% were injectables, 19% natalizumab, 7% fingolimod, and 5% rituximab. Patients who started treatment within 3 years after diagnosis were matched with patients who started treatment later.
Risk for Expanded Disability Status Score (EDSS) worsening to ≥4 (moderate disability in at least 1 domain) increased by 5% to 7% for each year of treatment delay (hazard ratio, 1…
Reviewing Author
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)