Natalizumab and fingolimod were associated with increased disease activity upon cessation.
Multiple sclerosis (MS) disease rebound — defined as more-severe disease than before treatment — has been described with discontinuation of natalizumab and of S1P inhibitors like fingolimod. To evaluate rebound further, investigators analyzed disease-modifying therapy (DMT) discontinuations in more than 14,000 patients in this retrospective, international, observational registry study.
After natalizumab, median time to the next therapy was 2 months. Relapses increased between months 2 and 4 for both those who did and those who did not start a new therapy. Annualized relapse rates (ARR) peaked at 4 to 6 months after natalizumab discontinuation (ARR 0.98; 95% confidence interval, 0.89–1.08). For fingolimod, stopping was due to lack of efficacy…
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)