Evidence map›Paper›PMID 40346603›Full record

SynthesisSystematic reviews2025

Comparative efficacy and acceptability of novel biologics in the treatment of myasthenia gravis: systematic review and network meta-analysis of randomized trials.

Chang Guan, Peixi Zhao, Meijin Song, Jing Lu, Huijing Cui, Dongxu Li, Tianying Chang, Yingzi Cui, Xikang Ding, Jian Wang and 1 more

Abstract readComparative StudyNetwork Meta-AnalysisSystematic Review
In one paragraph

Synthesis in Systematic reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
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

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

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

11 authors.

Chang Guan *College of Traditional Chinese Medicine, Changchun University of Traditional Chinese Medicine, Changchun, Jilin, 130117, China.
Peixi Zhao *College of Traditional Chinese Medicine, Changchun University of Traditional Chinese Medicine, Changchun, Jilin, 130117, China.
Meijin Song *College of Traditional Chinese Medicine, Changchun University of Traditional Chinese Medicine, Changchun, Jilin, 130117, China.
Jing LuThe Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, 130021, China.
Huijing CuiTraditional Chinese Medicine Department, Nanguan District Traditional Chinese Medicine Hospital, Changchun, Jilin, 130041, China.
Dongxu LiThe Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, 130021, China.
Tianying ChangThe Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, 130021, China.
Yingzi CuiThe Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, 130021, China.
Xikang DingThe Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, 130021, China.
Jian Wang *The Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, 130021, China. jian-w222@163.com.ORCID 0000-0003-1748-7305
Peng Xu *The Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, Jilin, 130021, China. xupeng@ccucm.edu.cn.ORCID 0000-0002-7008-1323

Funding

the National Key Research and Development Program of China No. 2022YFC3501301;2022YFC3501305the National Natural Science Foundation of China No. 82205107the Science and Technology Development Plan Project of Jilin Province, China No. 20210101212JCthe Yong Elite Scientists Sponsorship Program by CACM 2022-QNRC2-A08the Youth discipline backbone training project of Changchun university of Chinese Medicine 202310
6 · The paper itself

Abstract

backgroundMyasthenia gravis (MG) is a chronic autoimmune disorder affecting the neuromuscular junction. The emergence of molecular therapies, such as monoclonal antibodies, B-cell-depleting agents, and chimeric antigen receptor T-cell-based therapies, has the potential to transform the treatment landscape for myasthenia gravis. The clinical efficacy of novel biologics in the treatment of individuals with myasthenia gravis is still a subject of debate. The objective was to compare and rank the efficacy and acceptability of novel biologics in the treatment of individuals with MG through a network meta-analysis.

methodsThis systematic review and network meta-analysis (NMA) involved a comprehensive search for published randomized controlled trials (RCTs) across several databases, including PubMed, Web of Science, Embase, Cochrane Library, SinoMed, CNKI, Wanfang, and VIP, covering articles published from inception until July 3, 2024. We included randomized controlled trials involving patients with myasthenia gravis. The main outcome was the overall symptomatology. Random-effects pairwise meta-analyses and network meta-analyses (NMAs) were conducted to compute standardized mean differences (SMDs) or risk ratios with 95% confidence intervals (CIs). The research process did not include individuals with lived experience. The studies' quality was evaluated utilizing the risk-of-bias assessment tool created by the Cochrane Collaboration. Network meta-analysis was performed utilizing Stata 16 and R4.2.3.

resultsEleven RCTs including 840 participants with myasthenia gravis were eligible. Belimumab improvement of the MG-ADL score is compared to placebo (MD = - 3.29, 95% CI (- 5.78, - 0.80), P < 0.05). Compared to placebo, batoclimab enhanced the QMG score (MD = - 4.46, 95% CI (- 7.57, - 1.35), P < 0.05) and the MGC score (MD = - 3.58, 95% CI (- 6.68, - 0.47), P < 0.05). Eculizumab improvement of the MG-QoL 15r score is compared to placebo (MD = - 7.10, 95% CI (- 12.20, - 2.00), P < 0.05). Regarding adverse reactions, we found no difference in the network comparison of novel biologics compared to placebo, but this conclusion requires further validation through rigorous research.

conclusionsThis study provides an updated, relative rank-order efficacy of novel biologics therapies for myasthenia gravis. These data may help inform the design and sample size calculation of future clinical trials and assist selection of combination therapy. SYSTEMATIC REVIEW REGISTRATION: PROSPERO CRD42024559757.

Indexed as

Biological ProductsMyasthenia GravisAntibodies, Monoclonal, HumanizedHumansRandomized Controlled Trials as TopicTreatment OutcomeAntibodies, Monoclonal, HumanizedBiological ProductsEfficacy and acceptabilityMyasthenia gravisNetwork meta-analysisNovel biologics

Identifiers

PMID40346603
PMCPMC12063394

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.