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Real-world experience with ocrelizumab in the msbase registry.

Authors :
Hodgkinson S.
Spelman T.
Ozakbas S.
Kalincik T.
Boz C.
Buzzard K.
Skibina O.
Alroughani R.
Karabudak R.
Van Der Walt A.
Lechner-Scott J.
Taylor B.
Kermode A.
Mccombe P.
Duquette P.
Prat A.
Girard M.
Eichau Madueno S.
Izquierdo G.
Soysal A.
Sanchez-Menoyo J.L.
Sotoca J.
Muros-Le Rouzic E.
Dirks P.
Butzkueven H.
Laureys G.
Van Hijfte L.
Terzi M.
Butler E.
Macdonell R.
Patti F.
Van Pesch V.
Slee M.
Barnett M.
Grammond P.
Prevost J.
Grand-Maison F.
Hodgkinson S.
Spelman T.
Ozakbas S.
Kalincik T.
Boz C.
Buzzard K.
Skibina O.
Alroughani R.
Karabudak R.
Van Der Walt A.
Lechner-Scott J.
Taylor B.
Kermode A.
Mccombe P.
Duquette P.
Prat A.
Girard M.
Eichau Madueno S.
Izquierdo G.
Soysal A.
Sanchez-Menoyo J.L.
Sotoca J.
Muros-Le Rouzic E.
Dirks P.
Butzkueven H.
Laureys G.
Van Hijfte L.
Terzi M.
Butler E.
Macdonell R.
Patti F.
Van Pesch V.
Slee M.
Barnett M.
Grammond P.
Prevost J.
Grand-Maison F.
Publication Year :
2021

Abstract

Background: Ocrelizumab (OCR) is a humanised anti-CD20+ monoclonal antibody approved for the treatment of primary progressive multiple sclerosis (PPMS), and relapsing forms of MS, including both relapsing-remitting (RRMS) and secondary progressive MS (SPMS) with relapses. Objective(s): In a real-world setting, to describe 1) baseline characteristics of patients with MS treated with OCR, 2) treatment pathway across lines of therapy up to initiation of OCR, and 3) initial clinical experience in patients with >=6 months follow-up data from OCR initiation. Method(s): Secondary data analysis using MSBase Registry data including patients with a confirmed diagnosis of MS and started OCR therapy within 3 months prior to or at time of MSBase eligible/ initial visit. Descriptive statistics were used to analyze baseline patient characteristics' recorded within 3 months of OCR initiation, including demographics, disease course and duration, prior disease modifying therapies (DMT), and EDSS. Occurrence of relapse was analyzed in patients with >=6 months follow-up data from OCR initiation. Result(s): As of 4th June 2020, MSBase included 2531 patients newly treated with OCR, of whom 1679 had an EDSS evaluation within 3 months of OCR start. There were 1185 patients with RRMS, 236 with SPMS, and 183 with PPMS. Median age at OCR initiation was 41.9 years, 49.5 years, to 50.1 years in RRMS, SPMS, and PPMS, respectively. Mean disease duration from symptom onset up to OCR initiation was longer in SPMS (19.7 years) than in RRMS (10.6 years) and PPMS (9.7 years). OCR was initiated as first line therapy in 17.5%, 5.5%, and 54.2% of RRMS, SPMS, and PPMS patients respectively. Most frequent previous DMT's in RRMS were fingolimod (25.7%) and natalizumab (23.5%). 693 patients with RRMS had >=6 months followup during OCR exposure. Of these, 643 remained relapse free (93%; 95% CI 86.0, 100.0) over a mean OCR exposure of 1.23 years. The annualized relapse rate (ARR) was 0.08 (95% CI 0.06- 0.10)

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1305134116
Document Type :
Electronic Resource