Evidence map›Paper›PMID 42374283›Full record

ArticleBMC neurology2026

Switching from complement inhibitors in AQP4-IgG-positive NMOSD: clinical characteristics, an operational "cluster phase" and potential strategies to prevent therapeutic gaps.

Kenzo Sakurai, Kei Kaburagi, Kenji Isahaya, Hisanao Akiyama, Yoshihisa Yamano

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Article in BMC neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kenzo SakuraiDepartment of Neurology, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae, Kawasaki, Kanagawa, 216-8511, Japan. k2sakurai@marianna-u.ac.jp.ORCID https://orcid.org/0000-0002-9516-6753
Kei KaburagiDepartment of Neurology, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae, Kawasaki, Kanagawa, 216-8511, Japan.
Kenji IsahayaDepartment of Neurology, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae, Kawasaki, Kanagawa, 216-8511, Japan.
Hisanao AkiyamaDepartment of Neurology, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae, Kawasaki, Kanagawa, 216-8511, Japan.
Yoshihisa YamanoDepartment of Neurology, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae, Kawasaki, Kanagawa, 216-8511, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuromyelitis optica spectrum disorder (NMOSD) can cause severe neurological disability after a single relapse. Although relapse rates have markedly decreased with the emergence of targeted biologics, treatment switches are increasingly encountered due to long-term treatment considerations and adverse events. However, safe switching strategies, especially within 12 months after a relapse, which we defined operationally as the "cluster phase", have not been established. We investigated relapse risk and potential preventive strategies when switching from complement inhibitors in AQP4-IgG-positive NMOSD.

methodsWe retrospectively reviewed patients with AQP4-IgG-positive NMOSD treated at St. Marianna University School of Medicine who underwent at least one biologic switch. Clinical records were assessed for patient characteristics, treatment history, timing of switching, and relapse occurrence. Particular attention was given to switching from complement inhibitors during the cluster phase.

resultsAmong 14 patients who switched biologics, 5 switched from complement inhibitors, 4 switched between complement inhibitors, 2 between B-cell-depleting therapies, and 3 from IL-6 receptor inhibitors. Six of the 14 switches occurred during the cluster phase, including 3 from complement inhibitors (all to B-cell-depleting agents). One of the two patients switched without bridging therapy during the cluster phase experienced optic neuritis relapse, while no relapses occurred in the other 13 switching cases. This observation suggests a possible vulnerability during the cluster phase, although definitive conclusions cannot be drawn due to the small sample size.

conclusionsSwitching from complement inhibitors during the cluster phase may be associated with an increased susceptibility to relapse. Bridging strategies, such as plasma exchange or temporary biologic overlap, may help reduce the likelihood of therapeutic gaps, but these findings remain hypothesis-generating. Clinicians should proactively discuss future switching scenarios and develop long-term treatment plans with patients.

Indexed as

Aquaporin 4Complement Inactivating AgentsDrug SubstitutionImmunoglobulin GNeuromyelitis OpticaAdultFemaleHumansMaleMiddle AgedRecurrenceRetrospective StudiesAQP4 protein, humanAquaporin 4Complement Inactivating AgentsImmunoglobulin GAQP4-IgGBridging strategyCluster phaseComplement inhibitorNeuromyelitis optica spectrum disorderNo-gap strategyRelapseSwitching

Identifiers

PMID42374283
PMCPMC13580005

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.