Patients with primary-progressive MS and active disease had reduced risk for disease progression.
Multiple sclerosis (MS) classification now includes determination of disease activity and disease progression, regardless of the underlying MS subtype. Investigators retrospectively evaluated disease-modifying therapy (DMT) effectiveness in patients with primary-progressive (PP) MS patients with or without inflammatory activity. Out of a total of 3298 patients with PPMS, 665 met entry criteria for the ORATORIO trial of ocrelizumab, of whom 452 received a DMT. Because treated patients were younger and less disabled, 409 total patients were selected for propensity score matching.
Follow-up started when DMT use began or at first expanded disability status scale (EDSS) assessment if untreated. Mean follow-up was 11 years. The most common DMT was…
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)