Ocrelizumab as first-line therapy in highly active relapsing-remitting multiple sclerosis

In recent years, early use of highly effective disease modifying immunotherapies in relapsing-remitting multiple sclerosis (RRMS) demonstrated superior efficacy in preventing disability progression. For this study, we investigated ocrelizumab as first line therapy of RRMS in a monocentric, retrospective study. In our outpatient clinic, ocrelizumab was administered as first-line therapy in 33 patients with an anticipated highly active disease course. Patients were re-evaluated clinically every 6 months and at least annually with cranial magnetic resonance imaging (MRI), with a mean follow-up period of 27 months. Subgroup analyses were conducted based on age, sex, disease duration, and disability as measured by EDSS at initiation of therapy. Ocrelizumab therapy was administered within the first year of diagnosis. The median EDSS at the time of ocrelizumab initiation was 2.5, with male patients showing higher disability compared to the females. The annualized relapse rate (ARR) decreased from 2.24 to 0.058 during the observation period. EDSS remained stable throughout the therapy period for the entire cohort. Starting treatment earlier and at a lower initial EDSS correlated with a better outcome. Gender and age had no impact on the therapeutic efficacy. The most common infusion related reactions included fatigue (25 %) and headaches (9 %). Mild infections occurred in 21 % of patients. These data highlight the role of ocrelizumab as an effective first-line therapeutic approach for patients with highly active RRMS.

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Publication Details

Journal
Journal of the Neurological Sciences
Published
2025-06-06
DOI
https://doi.org/10.1016/j.jns.2025.123577
Citations
1
Primary Topic
Multiple Sclerosis Research Studies
Type
article
Field-Weighted Citation Impact
1.47
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article

Ocrelizumab as first-line therapy in highly active relapsing-remitting multiple sclerosis

Ralf A. Linker, Klemens Angstwurm, D. Freudenstein, De-Hyung Lee et al.
1 citations
Journal of the Neurological Sciences
Multiple Sclerosis Research Studies
1.47
article

Ocrelizumab as first-line therapy in highly active relapsing-remitting multiple sclerosis

Ralf A. Linker, Klemens Angstwurm, D. Freudenstein, De-Hyung Lee, Tamar Kvartskhava, Nicolas Sarmiento
article en
1 citations

Abstract

In recent years, early use of highly effective disease modifying immunotherapies in relapsing-remitting multiple sclerosis (RRMS) demonstrated superior efficacy in preventing disability progression. For this study, we investigated ocrelizumab as first line therapy of RRMS in a monocentric, retrospective study. In our outpatient clinic, ocrelizumab was administered as first-line therapy in 33 patients with an anticipated highly active disease course. Patients were re-evaluated clinically every 6 months and at least annually with cranial magnetic resonance imaging (MRI), with a mean follow-up period of 27 months. Subgroup analyses were conducted based on age, sex, disease duration, and disability as measured by EDSS at initiation of therapy. Ocrelizumab therapy was administered within the first year of diagnosis. The median EDSS at the time of ocrelizumab initiation was 2.5, with male patients showing higher disability compared to the females. The annualized relapse rate (ARR) decreased from 2.24 to 0.058 during the observation period. EDSS remained stable throughout the therapy period for the entire cohort. Starting treatment earlier and at a lower initial EDSS correlated with a better outcome. Gender and age had no impact on the therapeutic efficacy. The most common infusion related reactions included fatigue (25 %) and headaches (9 %). Mild infections occurred in 21 % of patients. These data highlight the role of ocrelizumab as an effective first-line therapeutic approach for patients with highly active RRMS.

Journal of the Neurological SciencesVol. 475
University Hospital Regensburg (DE), Technische Hochschule Ingolstadt (DE)
Openalex Percentile: Top 19%
Multiple Sclerosis Research Studies
1.47
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