Evidence map›Paper›PMID 41379391›Full record

ArticleJournal of neurology2025

A pilot study of telitacicept in predominantly immune-mediated necrotizing myopathy, retrospective analysis of a monocentric Chinese cohort.

Wei Xiang, Yijun Ren, Huan Yang

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Article in Journal 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Wei XiangDepartment of Neurology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410018, Hunan, China.
Yijun RenDepartment of Neurology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410018, Hunan, China.
Huan YangDepartment of Neurology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410018, Hunan, China. 403850@csu.edu.cn.ORCID http://orcid.org/0000-0002-8690-2544

Funding

National Natural Science Foundation of China 82171399National Natural Science Foundation of China 82371413
6 · The paper itself

Abstract

backgroundIdiopathic inflammatory myopathies (IIM) are a group of rare autoimmune disorders mainly involving skeletal muscles. Telitacicept is a BAFF/APRIL inhibitor, which has a promising application in B-cell-mediated autoimmune diseases; however, its efficacy in IIM patients is still unknown.

methodsRetrospective analysis of 15 IIM patients treated with telitacicept for more than 6 months in Xiangya Hospital between November 2023 and May 2025. Core clinical measures and glucocorticoid (GCS) dosage at baseline, 3 months, 6 months, and final follow-up were recorded. The treatment was evaluated according to the total improvement score (TIS) defined by the 2016 ACR/EULAR myositis response criteria.

resultsIn the final follow-up, 11 patients (73.33%) had improved clinical symptoms after 8 months of median treatment. Significant improvements were observed in physician/patient global assessments (PhGA/PtGA), manual muscle testing (MMT-8), health assessment questionnaire (HAQ) score, and creatine kinase (CK) levels (all p < 0.05). The average GCS dose dropped from 23.67 ± 18.37 to 11.00 ± 11.05 mg/d (p = 0.006). Serum IgG (p = 0.018), IgA (p < 0.001), and IgM (p < 0.001) decreased, while C3 (p = 0.001) and C4 (p = 0.030) increased. No serious drug-related adverse events occurred.

conclusionsTelitacicept may be an effective and safety-promising therapeutic option for IIM, especially IMNM patients. Larger randomized controlled trials are required to confirm these findings.

Indexed as

MyositisAdultAgedEast Asian PeopleFemaleFollow-Up StudiesHumansMaleMiddle AgedPilot ProjectsRecombinant Fusion ProteinsRetrospective StudiesYoung AdultRecombinant Fusion ProteinstelitaciceptEfficacyIdiopathic inflammatory myopathyImmune-mediated necrotizing myopathySafetyTelitaciceptTreatment

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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.