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. 2025 Jan 15:468:123356.
doi: 10.1016/j.jns.2024.123356. Epub 2024 Dec 16.

Ofatumumab for multiple sclerosis with disability accumulation

Affiliations

Ofatumumab for multiple sclerosis with disability accumulation

Masahiro Mimori et al. J Neurol Sci. .

Abstract

Background: The ASCLEPIOS/APLIOS/APOLITOS/ALITHIOS trials highlighted the benefits of ofatumumab in reducing relapse rates and disability progression in multiple sclerosis (MS). However, its effects on patients with severe disability status remains uncertain. This study aimed to clarify the outcomes of ofatumumab in MS patients with high Expanded Disability Status Scale (EDSS) scores and prolonged disease durations.

Methods: This is a retrospective cohort study of MS patients treated with ofatumumab at an MS center in Japan. At 12 months of treatment, patients with MS starting ofatumumab were classified into the treatment-responsive or treatment-resistant groups based on ofatumumab continuity, incidence of relapses with EDSS worsening, progression independent of relapse activity (PIRA). We used logistic regression analysis to identify factors associated with ofatumumab response.

Results: Seventy patients were included in the analysis; 39 (56 %) patients were relapsing-remitting (RR), and 31 (44 %) patients were secondary progressive (SP) MS. Mean age at ofatumumab initiation, age at onset, and disease duration were 48.0, 33.9, and 14.1 years, respectively. The median EDSS was 4.5 (3.0-6.5); 38(56 %) patients were classified as resistant. The resistant rates by disease type were 33 % (13/39) and 81 % (26/31) for RR and SP MS, respectively. On multivariate analysis, EDSS and No evidence of disease activity (NEDA) 3 were independent factors for ofatumumab responsiveness (OR, 1.74, 0.04; 95 % CI, 1.17-2.73, 0.00-0.47; p = 0.01, 0.04).

Conclusion: Ofatumumab may yield more favorable effects when initiated in patients with MS with lower EDSS scores.

Keywords: Disease-modifying drugs; Ofatumumab; Progressive multiple sclerosis; Relapsing-remitting multiple sclerosis.

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Conflict of interest statement

Declaration of competing interest MM, AK, and YT have no conflicts of interest related to this study to disclose. TO received lecture fees from CSL Behring KK research grants from Takeda Pharma, PPD-SNBL KK, Argenx, and Janssen Pharmaceutical KK. YL served as the principal investigator for clinical trials of ofatumumab and received lecture fees from Novartis Pharma, Mitsubishi Tanabe Pharma, Alexion Pharma, Takeda Pharma, and Asahikasei Medical. WS received speaker honoraria from Biogen, Novartis Pharma, Chugai, Mitsubishi Tanabe Pharma and Takeda Pharma. TY served on scientific advisory boards for Biogen Japan, Biogen MA, and Novartis Pharma; received research grants from Novartis Pharma, Biogen Japan, Chiome Bioscience, Sanofi, UCB Japan, and Mebix; and received speaker honoraria from Biogen Japan, Novartis Pharma, Mitsubishi Tanabe Pharma, Takeda Pharma, Miyarisan Pharmaceutical, Sumitomo Pharma, and Teijin Pharma.

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