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Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis
BACKGROUND: Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered. OBJECTIVE: The aim of this study was to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313157/ https://www.ncbi.nlm.nih.gov/pubmed/32607256 http://dx.doi.org/10.1155/2020/5463451 |
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author | Daniels, K. van der Nat, P. B. Frequin, S. T. F. M. van der Wees, P. J. Biesma, D. H. Hoogervorst, E. L. J. van de Garde, E. M. W. |
author_facet | Daniels, K. van der Nat, P. B. Frequin, S. T. F. M. van der Wees, P. J. Biesma, D. H. Hoogervorst, E. L. J. van de Garde, E. M. W. |
author_sort | Daniels, K. |
collection | PubMed |
description | BACKGROUND: Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered. OBJECTIVE: The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting. METHODS: We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (n = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration). RESULTS: Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (Z = −2.81, p ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start. CONCLUSION: Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab. |
format | Online Article Text |
id | pubmed-7313157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-73131572020-06-29 Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis Daniels, K. van der Nat, P. B. Frequin, S. T. F. M. van der Wees, P. J. Biesma, D. H. Hoogervorst, E. L. J. van de Garde, E. M. W. Mult Scler Int Research Article BACKGROUND: Recently, ocrelizumab (Ocrevus®) was approved for the treatment of primary progressive multiple sclerosis (PPMS) based on data from the ORATORIO clinical trial. Real-world data about the clinical effectiveness of ocrelizumab has yet to be gathered. OBJECTIVE: The aim of this study was to provide data about the clinical effectiveness of ocrelizumab for patients diagnosed with PPMS in a real-world setting. METHODS: We conducted a retrospective cohort study of all patients with PPMS who started ocrelizumab treatment (n = 21) in St. Antonius Hospital (Utrecht/Nieuwegein, the Netherlands) between April 2018 and December 31, 2018. Primary outcome was pre- versus post-ocrelizumab disability worsening rate (from 96 weeks prior to first ocrelizumab administration up to 24 weeks post first ocrelizumab administration). RESULTS: Disability worsening rate while on treatment significantly differed (lower) from disability worsening rate in pre-treatment period (Z = −2.81, p ≤ .01). Three out of 17 patients showed a clinically relevant improvement in disability status after treatment start. CONCLUSION: Ocrelizumab can stabilize disability progression in patients with PPMS. Some patients even showed a clinically relevant improvement in disability status. Further research should help to identify which patients benefit most from ocrelizumab. Hindawi 2020-06-15 /pmc/articles/PMC7313157/ /pubmed/32607256 http://dx.doi.org/10.1155/2020/5463451 Text en Copyright © 2020 K. Daniels et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Daniels, K. van der Nat, P. B. Frequin, S. T. F. M. van der Wees, P. J. Biesma, D. H. Hoogervorst, E. L. J. van de Garde, E. M. W. Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis |
title | Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis |
title_full | Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis |
title_fullStr | Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis |
title_full_unstemmed | Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis |
title_short | Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis |
title_sort | real-world results of ocrelizumab treatment for primary progressive multiple sclerosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313157/ https://www.ncbi.nlm.nih.gov/pubmed/32607256 http://dx.doi.org/10.1155/2020/5463451 |
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