Evidence map›Paper›PMID 40492601›Full record

ArticleAnnals of clinical and translational neurology2025

Factors for Rituximab Refractoriness in AQP4-IgG+ NMOSD: A Cohort Study.

Mariano Marrodan, María A Piedrabuena, María A Zarate, Sofía Rodríguez Murúa, Ezequiel I Surace, Mauricio F Farez, Marcela P Fiol, María C Ysrraelit, Jorge Correale

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Article in Annals of clinical and translational neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Mariano MarrodanDepartamento de Neurología, Fleni, Buenos Aires, Argentina.ORCID 0000-0002-4142-8375
María A PiedrabuenaDepartamento de Neurología, Fleni, Buenos Aires, Argentina.
María A ZarateDepartamento de Neurología, Fleni, Buenos Aires, Argentina.
Sofía Rodríguez MurúaCentro de Investigación en Enfermedades Neuroinmunológicas (CIEN), Fleni, Buenos Aires, Argentina.
Ezequiel I SuraceLaboratorio de Enfermedades Neurodegenerativas, Instituto de Neurociencias Fleni-CONICET (Consejo Nacional de Investigaciones Científicas y Tecnológicas), Buenos Aires, Argentina.ORCID 0000-0001-8492-9578
Mauricio F FarezDepartamento de Neurología, Fleni, Buenos Aires, Argentina.
Marcela P FiolDepartamento de Neurología, Fleni, Buenos Aires, Argentina.
María C YsrraelitDepartamento de Neurología, Fleni, Buenos Aires, Argentina.
Jorge CorrealeDepartamento de Neurología, Fleni, Buenos Aires, Argentina.

Funding

AstraZeneca
6 · The paper itself

Abstract

objectiveNeuromyelitis optica spectrum disorder (NMOSD) is a severe autoimmune condition of the central nervous system (CNS), often associated with aquaporin-4 antibodies (AQP4-IgG). Rituximab, a CD20+ B-cell depleting monoclonal antibody, is widely used as first-line therapy. However, a subset of patients exhibits treatment refractoriness. Our objective is to investigate factors associated with treatment refractoriness in AQP4-IgG-positive NMOSD patients treated with rituximab.

methodsThis retrospective cohort study included 54 AQP4-IgG-positive NMOSD patients treated with rituximab between 2006 and 2023. Clinical, imaging, and genetic data were analyzed. Treatment failure was defined as at least one relapse occurring after 6 months of rituximab initiation. Statistical analyses included multivariate analyses of covariance (MANCOVA) and Cox regression to identify independent predictors of treatment failure.

resultsAmong the 54 patients (82.5% female, median age 45 years, range: 34-54.5), 12 (22.2%) exhibited rituximab treatment failure. The presence of asymptomatic lesions during follow-up was significantly associated with treatment failure (p = 0.02) and emerged as an independent predictor in MANCOVA (Wilks' Lambda = 0.01, F = 20.5, η

interpretationAsymptomatic lesions during rituximab treatment are a strong predictor of therapeutic failure in AQP4-IgG-positive NMOSD patients. Early identification of these lesions could guide clinicians in optimizing treatment strategies, including transitioning to alternative therapies.

Indexed as

Aquaporin 4Immunologic FactorsNeuromyelitis OpticaRituximabAdultAutoantibodiesCohort StudiesFemaleHumansImmunoglobulin GMaleMiddle AgedRetrospective StudiesTreatment FailureAQP4 protein, humanAquaporin 4AutoantibodiesImmunoglobulin GImmunologic FactorsRituximabneuromyelitis optica spectrum disordersNMOSDrituximab

Identifiers

PMID40492601
PMCPMC12343303

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