Evidence map›Paper›PMID 41081809›Full record

ArticleAnnals of Indian Academy of Neurology2025

Efficacy and Safety of Telitacicept and Mycophenolate Mofetil in the Treatment of Neuromyelitis Optica Spectrum Disorders.

Shaomin Zuo, Wenning Yang, Xiaojuan Wang, Milan Zhang, Zeqin Dong, Xin Chen, Wei Li

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Article in Annals of Indian Academy of Neurology, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shaomin ZuoDepartment of Neurology, People's Hospital of Henan University, Zhengzhou, Henan Province, China.
Wenning YangDepartment of Neurology, People's Hospital of Henan University, Zhengzhou, Henan Province, China.
Xiaojuan WangDepartment of Neurology, People's Hospital of Henan Provincial, Zhengzhou, Henan Province, China.
Milan ZhangDepartment of Neurology, People's Hospital of Henan Provincial, Zhengzhou, Henan Province, China.
Zeqin DongDepartment of Neurology, People's Hospital of Henan University, Zhengzhou, Henan Province, China.
Xin ChenDepartment of Neurology, People's Hospital of Xinxiang Medical University, Zhengzhou, China.
Wei LiDepartment of Neurology, People's Hospital of Henan Provincial, Zhengzhou, Henan Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesTo compare the efficacy and safety of telitacicept versus mycophenolate mofetil (MMF) in reducing relapses and disability in adults with neuromyelitis optica spectrum disorder (NMOSD).

methodsIn this retrospective cohort study, we analyzed 41 adults with NMOSD (2015 diagnostic criteria). Patients received ≥6 months of telitacicept or MMF treatment. Primary outcomes were annualized relapse rate (ARR) and relapse-free survival; secondary outcomes included Expanded Disability Status Scale (EDSS) score, CD19 + B-cell count, and safety.

resultsOver a median follow-up of 8 months for telitacicept (n = 15) and 9 months for MMF (n = 26), patients receiving telitacicept exhibited an 86.7% relapse-free rate (13/15) versus 57.6% (15/26) with MMF, with a significantly prolonged time to first relapse (hazard ratio 0.22, 95% confidence interval: 0.05-0.91; P = 0.04). The magnitude of ARR reduction was significantly greater with telitacicept (median ΔARR 2.0 [interquartile range (IQR) 2.0-4.0]) than with MMF (2.0 [1.0-2.0]; P = 0.007). Neurological function improved markedly, evidenced by a 2.5-point reduction (IQR: 2.0-3.0) in EDSS scores with telitacicept versus 0.5 points (IQR: 0.5-1.0) for MMF ( P < 0.001). Mechanistically, telitacicept induced deeper CD19 + B-cell suppression (Δ51.0 cells/μL [42.0-70.0]) than MMF (Δ28.5 cells/μL [8.0-40.2]; P = 0.002). Safety profiles favored telitacicept, with adverse events occurring in 20.0% (3/15) versus 42.3% (11/26) in the MMF group, though no severe events were observed in either cohort.

conclusionBoth telitacicept and MMF demonstrated favorable clinical efficacy and safety in NMOSD treatment. Compared with MMF, telitacicept exhibits potential advantages and holds promising prospects for clinical application.

Indexed as

mycophenolate mofetilNeuromyelitis optica spectrum disordertelitacicept

Identifiers

PMID41081809
PMCPMC12610963

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