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Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study
BACKGROUND: Exit strategy after natalizumab cessation in multiple sclerosis (MS) is a crucial point because the risk of disease reactivation is high during this period. The objective of this observational study was to compare ocrelizumab to fingolimod after natalizumab cessation in patients with rel...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725429/ https://www.ncbi.nlm.nih.gov/pubmed/34982200 http://dx.doi.org/10.1007/s00415-021-10950-7 |
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author | Bigaut, Kévin Kremer, Laurent Fabacher, Thibaut Ahle, Guido Goudot, Mathilde Fleury, Marie Gaultier, Claude Courtois, Sylvie Collongues, Nicolas de Seze, Jérôme |
author_facet | Bigaut, Kévin Kremer, Laurent Fabacher, Thibaut Ahle, Guido Goudot, Mathilde Fleury, Marie Gaultier, Claude Courtois, Sylvie Collongues, Nicolas de Seze, Jérôme |
author_sort | Bigaut, Kévin |
collection | PubMed |
description | BACKGROUND: Exit strategy after natalizumab cessation in multiple sclerosis (MS) is a crucial point because the risk of disease reactivation is high during this period. The objective of this observational study was to compare ocrelizumab to fingolimod after natalizumab cessation in patients with relapsing–remitting multiple sclerosis (RRMS). METHODS: All RRMS patients starting fingolimod or ocrelizumab within 6 weeks after natalizumab cessation were included. The primary endpoint was the annualized relapse rate (ARR) at 1 year. RESULTS: We included 54 patients receiving fingolimod and 48 patients receiving ocrelizumab after natalizumab cessation. In multivariate analysis, ARR at 1 year was significantly lower in the ocrelizumab group than in the fingolimod group (0.12 ± 0.39 versus 0.41 ± 0.71, p = 0.026), i.e. a 70.7% lower relapse rate. The cumulative probability of relapses at 1 year was 31.5% (17/54 patients) with fingolimod and 10.4% (5/48 patients) with ocrelizumab, corresponding to a hazard ratio of 3.4 (95% confidence interval: 1.1–11, p = 0.04). CONCLUSIONS: Our results suggest ocrelizumab is potentially a better exit strategy than fingolimod after natalizumab cessation. |
format | Online Article Text |
id | pubmed-8725429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-87254292022-01-04 Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study Bigaut, Kévin Kremer, Laurent Fabacher, Thibaut Ahle, Guido Goudot, Mathilde Fleury, Marie Gaultier, Claude Courtois, Sylvie Collongues, Nicolas de Seze, Jérôme J Neurol Original Communication BACKGROUND: Exit strategy after natalizumab cessation in multiple sclerosis (MS) is a crucial point because the risk of disease reactivation is high during this period. The objective of this observational study was to compare ocrelizumab to fingolimod after natalizumab cessation in patients with relapsing–remitting multiple sclerosis (RRMS). METHODS: All RRMS patients starting fingolimod or ocrelizumab within 6 weeks after natalizumab cessation were included. The primary endpoint was the annualized relapse rate (ARR) at 1 year. RESULTS: We included 54 patients receiving fingolimod and 48 patients receiving ocrelizumab after natalizumab cessation. In multivariate analysis, ARR at 1 year was significantly lower in the ocrelizumab group than in the fingolimod group (0.12 ± 0.39 versus 0.41 ± 0.71, p = 0.026), i.e. a 70.7% lower relapse rate. The cumulative probability of relapses at 1 year was 31.5% (17/54 patients) with fingolimod and 10.4% (5/48 patients) with ocrelizumab, corresponding to a hazard ratio of 3.4 (95% confidence interval: 1.1–11, p = 0.04). CONCLUSIONS: Our results suggest ocrelizumab is potentially a better exit strategy than fingolimod after natalizumab cessation. Springer Berlin Heidelberg 2022-01-04 2022 /pmc/articles/PMC8725429/ /pubmed/34982200 http://dx.doi.org/10.1007/s00415-021-10950-7 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Communication Bigaut, Kévin Kremer, Laurent Fabacher, Thibaut Ahle, Guido Goudot, Mathilde Fleury, Marie Gaultier, Claude Courtois, Sylvie Collongues, Nicolas de Seze, Jérôme Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study |
title | Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study |
title_full | Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study |
title_fullStr | Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study |
title_full_unstemmed | Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study |
title_short | Ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study |
title_sort | ocrelizumab versus fingolimod after natalizumab cessation in multiple sclerosis: an observational study |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725429/ https://www.ncbi.nlm.nih.gov/pubmed/34982200 http://dx.doi.org/10.1007/s00415-021-10950-7 |
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