Real-World Results of Ocrelizumab Treatment for Primary Progressive Multiple Sclerosis
Autor: | 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, Afd Pharmacoepi & Clinical Pharmacology, Pharmacoepidemiology and Clinical Pharmacology |
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Přispěvatelé: | Afd Pharmacoepi & Clinical Pharmacology, Pharmacoepidemiology and Clinical Pharmacology |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Article Subject Clinical effectiveness business.industry Multiple sclerosis MEDLINE Retrospective cohort study Primary Progressive Multiple Sclerosis medicine.disease Healthcare improvement science Radboud Institute for Health Sciences [Radboudumc 18] Clinical trial 03 medical and health sciences 0302 clinical medicine Internal medicine medicine Ocrelizumab In patient Neurology. Diseases of the nervous system 030212 general & internal medicine Neurology (clinical) RC346-429 business 030217 neurology & neurosurgery Research Article medicine.drug |
Zdroj: | Multiple Sclerosis International, 2020 Multiple Sclerosis International, Vol 2020 (2020) Multiple Sclerosis International, 2020. Hindawi Publishing Corporation Multiple Sclerosis International |
ISSN: | 2090-2654 |
Popis: | 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. |
Databáze: | OpenAIRE |
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