Evidence map›Paper›PMID 39628891›Full record

ArticleFrontiers in neurology2024

Efgartigimod treatment in patients with anti-MuSK-positive myasthenia gravis in exacerbation.

Fangyi Shi, Jiaxin Chen, Li Feng, Rong Lai, Hongyan Zhou, Xunsha Sun, Cunzhou Shen, Jiezhen Feng, Huiyu Feng, Haiyan Wang

Abstract read
In one paragraph

Article in Frontiers in neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

10 authors.

Fangyi Shi *Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jiaxin Chen *Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Li FengDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Rong LaiDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Hongyan ZhouDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xunsha SunDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Cunzhou ShenDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jiezhen FengDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Huiyu FengDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Haiyan WangDepartment of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The prevalence of patients positive for muscle-specific kinase antibody (hereafter, MuSK-Ab) accounts for 5-8% of all myasthenia gravis (MG) cases. Currently, efgartigimod has shown good therapeutic effects in MUSK-Ab-positive MG patients in a phase III clinical trial. However, phase III clinical trials tend to exclude MG patients in exacerbation, and there are only few real-world studies on the efficacy of efgartigimod in MuSK-Ab-positive myasthenic crisis (MC) patients. This retrospective, real-world study aimed to explore the efficacy of efgartigimod in MuSK-Ab-positive MG with exacerbation. Methods: We reviewed the clinical data of four MuSK-Ab-positive patients with exacerbation of MG who received efgartigimod at the First Affiliated Hospital of Sun Yat-sen University, including two patients with MC. All patients were admitted between September 2023 and May 2024. Most patients are simultaneously undergoing rituximab treatment. Results: Each patient completed one cycle of efgartigimod. After the first administration, four patients showed a clinically meaningful decrease in the Myasthenia Gravis Activities of Daily Living (MG-ADL) score (a reduction of more than 4 points compared to baseline), and all patients showed a decrease in IgG levels after one cycle of efgartigimod. Regarding safety, none of the patients experienced any obvious adverse effects. At the final follow-up, all patients achieved the minimal symptom expression status (an MG-ADL score of 0 or 1) following the first administration of efgartigimod for 8.75 ± 5.56 weeks. This article presents a case involving a patient who exhibited prompt alleviation of symptoms following the administration of a high dose of efgartigimod (20 mg/kg, given on days 1 and 5), without the use of any other fast-acting treatment. Conclusion: This retrospective real-world study demonstrates the effectiveness and safety of efgartigimod in these four MuSK-Ab-positive, female Asian patients with exacerbation of MG, as well as in patients experiencing MC. It is important to note that efgartigimod should not be viewed as a substitute for foundational immunotherapy; rather, it is intended as a rescue treatment during exacerbations and as an adjunctive therapy in the context of long-term immunotherapy. This non-invasive approach has the potential to become another treatment option for MuSK-Ab-positive MG patients.

Indexed as

efgartigimodexacerbationMuSK antibodiesmyasthenia gravismyasthenic crisis

Identifiers

PMID39628891
PMCPMC11611843

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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.