A Retrospective Evaluation of Ocrelizumab and Rituximab Discontinuation in a Real-World Patient Cohort

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Authors: David Jure Hunt, Nathan Chu, Dian Kuipers, Jomana Morkous, Kyra West, Christopher Uy, Mohammad Salem Alhalabi, Ana‐Luiza Sayao, Anthony Traboulsee, Robert Carruthers, Virginia Devonshire, Alice Schabas
Cited by: 2

Abstract

ABSTRACT Background: Ocrelizumab (OCR) and rituximab (RTX) are anti-CD20 monoclonal antibodies (CD20Mabs) used in the treatment of relapsing multiple sclerosis (RMS). While both are effective at reducing relapses and new MRI lesions in clinical trials, real-world data on discontinuation rates and reasons for stopping therapy are limited. Methods: This observational retrospective chart review included patients from two MS clinics in British Columbia, Canada. RMS patients treated with at least one infusion of OCR or RTX between January 2017 and March 2023 were included. Primary outcomes were reasons for discontinuation and discontinuation rates, with a secondary outcome of time to discontinuation. Results: In total, 881 RMS patients were included, with 478 on OCR and 403 on RTX. A total of 16.9% of patients on OCR and 14.9% on RTX discontinued therapy over 1643 and 694 patient-years, respectively ( p = 0.46). Reasons for discontinuation included: side effects (33.3%), insurance coverage (17.0%) and clinical or radiological disease activity (11.3%). Discontinuation rates at 12, 24 and 36 months were 3.5%, 8.2% and 12.5% for OCR, and 6.4%, 14.8% and 22.2% for RTX, respectively ( p = 0.0089). Median time to discontinuation was 21 months on OCR and 11.5 months on RTX ( p < 0.0001). On Cox regression analysis, treatment with RTX was the only variable associated with discontinuation (hazard ratio 1.72, 95% CI 1.20–2.45). Conclusion: Discontinuation rates of CD20Mabs were low, and the most common reason for stopping was side effects. Although not designed for comparison, our study suggests RMS patients may persist longer on OCR than RTX.

Fields of Study & Subjects

Pancreatitis Pathology and Treatment Peripheral Neuropathies and Disorders IgG4-Related and Inflammatory Diseases

Publication details

Journal / source
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
Publisher
Cambridge University Press (CUP)
Pages
1–9
Publication date
9 January 2026
Language
EN