{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,29]],"date-time":"2025-08-29T10:21:19Z","timestamp":1756462879461,"version":"3.41.2"},"reference-count":31,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/100004337","name":"Roche","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100004337","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Multiple Sclerosis Journal - Experimental, Translational and Clinical"],"published-print":{"date-parts":[[2025,1]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p> Persistence to B cell depleting therapies (BCDT) like ocrelizumab and rituximab may be higher compared with other disease-modifying therapies (DMT) in multiple sclerosis (MS). Clinical trials directly comparing these treatments are lacking. <\/jats:p><\/jats:sec><jats:sec><jats:title>Objective<\/jats:title><jats:p> To compare the risk of treatment discontinuation, relapse, and confirmed disability worsening in patients starting BCDT vs other DMT within real-world settings. <\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p> In a longitudinal cohort study, patients with relapsing MS starting BCDT (ocrelizumab\/rituximab, n\u2009=\u2009269) after enrolment into the Swiss MS Cohort (SMSC) were evaluated for treatment discontinuation, occurrence of relapses, and disability worsening in comparison with platform ( n\u2009=\u200957) and oral ( n\u2009=\u2009454) DMT, or natalizumab ( n\u2009=\u200973) using Cox regression with double robust adjustment for baseline covariates. <\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p> Patients starting BCDT were less likely to discontinue treatment than all other DMT combined (HR\u2009=\u20090.26, 95% CI\u2009=\u20090.18\u20130.36, p\u2009&lt;\u2009.01), oral DMT (HR\u2009=\u20090.28, 95% CI\u2009=\u20090.20\u20130.39, p\u2009&lt;\u2009.01) and natalizumab (HR\u2009=\u20090.35, 95% CI\u2009=\u20090.21\u20130.58, p\u2009&lt;\u2009.01). BCDT were associated with lower risk of relapses as compared to oral DMT HR\u2009=\u20090.59, 95% CI\u2009=\u20090.39\u20130.88, p\u2009&lt;\u2009.01), but not to natalizumab (HR\u2009=\u20090.90, 95% CI\u2009=\u20090.45\u20131.82, p\u2009=\u2009.778). Disability worsening was not significantly different between treatment groups. <\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p> We provide real-world evidence for patients being more persistent to BCDT than to other treatments, and better clinical outcomes may partly explain this. <\/jats:p><\/jats:sec>","DOI":"10.1177\/20552173251315457","type":"journal-article","created":{"date-parts":[[2025,2,27]],"date-time":"2025-02-27T06:26:57Z","timestamp":1740637617000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":1,"title":["Treatment persistence and clinical outcomes in patients starting B cell depleting therapies within the Swiss MS Cohort"],"prefix":"10.1177","volume":"11","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8512-6096","authenticated-orcid":false,"given":"Giulio","family":"Disanto","sequence":"first","affiliation":[{"name":"Multiple Sclerosis Center, Department of Neurology, 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