A high proportion of patients with early, aggressive MS achieved no evidence of disease activity in this phase II trial.
To evaluate multiple sclerosis (MS) progression after autologous hematopoietic stem cell transplantation with high-dose immunosuppressive therapy, researchers initiated a 5-year, multicenter, phase II, open-label study. They now report interim, 3-year results. The investigators recruited patients with active, early MS who had failed previous therapies. At baseline, the 24 participants typically had moderate disability, a median age of 38, had MS for 4.9 years, and had failed three previous MS medications. After mobilization of peripheral blood stem cells and before engraftment, participants received high-dose chemotherapy with carmustine, etoposide, cytarabine, and melphalan. The primary outcome was time to treatment failure (death, disabil…
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)