Real World Effectiveness and Tolerability of Novel Monoclonal Antibodies and Rituximab for NMOSD

In this multicenter retrospective cohort study of 135 people with aquaporin-4 IgG+ neuromyelitis optica spectrum disorder (NMOSD), some of whom were exposed to multiple therapies, we evaluated the effectiveness and tolerability of rituximab (n = 111) and novel monoclonal antibodies (nMAbs): eculizumab (n = 9), inebilizumab (n = 23), and satralizumab (n = 14). Over a median follow-up of 3.92 years, 21/111 rituximab-treated patients relapsed. In contrast, relapse occurred in only 1/23 inebilizumab-treated patients (median follow-up 1.27 years), with no relapses observed in those receiving eculizumab or satralizumab. Twelve-month relapse-free probabilities were 92% (rituximab), 94% (inebilizumab), and 100% (eculizumab and satralizumab). Among those with available MRI data, 10/73 rituximab and 1/14 inebilizumab developed new lesions. There were no serious adverse events. These findings support nMAbs as effective and well-tolerated first-line therapies for NMOSD.

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Publication Details

Journal
Annals of Clinical and Translational Neurology
Published
2025-08-22
DOI
https://doi.org/10.1002/acn3.70160
Citations
2
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
Field-Weighted Citation Impact
2.94

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article

Real World Effectiveness and Tolerability of Novel Monoclonal Antibodies and Rituximab for NMOSD

Amy Kunchok, Daniel Ontaneda, Le H. Hua, Justin Abbatemarco et al.
2 citations
Annals of Clinical and Translational Neurology
Systemic Sclerosis and Related Diseases
2.94
article

Real World Effectiveness and Tolerability of Novel Monoclonal Antibodies and Rituximab for NMOSD

Amy Kunchok, Daniel Ontaneda, Le H. Hua, Justin Abbatemarco, Mengke Du, Mary R. Rensel, Carrie M. Hersh, Devon Conway, Jeffrey Cohen, Zarmina Javed
article en
2 citations

Abstract

In this multicenter retrospective cohort study of 135 people with aquaporin-4 IgG+ neuromyelitis optica spectrum disorder (NMOSD), some of whom were exposed to multiple therapies, we evaluated the effectiveness and tolerability of rituximab (n = 111) and novel monoclonal antibodies (nMAbs): eculizumab (n = 9), inebilizumab (n = 23), and satralizumab (n = 14). Over a median follow-up of 3.92 years, 21/111 rituximab-treated patients relapsed. In contrast, relapse occurred in only 1/23 inebilizumab-treated patients (median follow-up 1.27 years), with no relapses observed in those receiving eculizumab or satralizumab. Twelve-month relapse-free probabilities were 92% (rituximab), 94% (inebilizumab), and 100% (eculizumab and satralizumab). Among those with available MRI data, 10/73 rituximab and 1/14 inebilizumab developed new lesions. There were no serious adverse events. These findings support nMAbs as effective and well-tolerated first-line therapies for NMOSD.

Annals of Clinical and Translational NeurologyVol. 12(10)
Cleveland Clinic (US), Lou Ruvo Brain Institute (US), Quantitative BioSciences (US)
Amgen, Bristol-Myers Squibb, Sanofi, Biogen, Patient-Centered Outcomes Research Institute, Alexion Pharmaceuticals, TG Therapeutics, Race to Erase MS, Horizon Therapeutics, Multiple Sclerosis Society, National Institutes of Health, Agency for Healthcare Research and Quality, Genentech, EMD Serono, National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 8%
Systemic Sclerosis and Related Diseases
2.94
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