[Pubmed] Efgartigimod-alfa therapy in acetylcholine receptor antibody myasthenia gravis: Romanian experience

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[Pubmed] Efgartigimod-alfa therapy in acetylcholine receptor antibody myasthenia gravis: Romanian experience

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Front Neurol. 2026 Sep 3;17:1945691. doi: 10.3389/fneur.2026.1945691. eCollection 2026.

ABSTRACT

BACKGROUND: Efgartigimod alfa, the first neonatal Fc receptor inhibitor approved for the treatment of acetylcholine receptor antibody (AChR)-positive generalized myasthenia gravis (MG), has demonstrated efficacy in randomized controlled trials. However, real-world data, particularly from Eastern Europe, remain limited.

METHODS: This prospective, multicenter study enrolled AChR-positive generalized MG patients treated with efgartigimod across six Romanian university hospitals between March 2024 and September 2025. Outcomes were assessed using the Myasthenia Gravis Activities of Daily Living (MG-ADL) scale, the Quantitative Myasthenia Gravis (QMG) score, and the Myasthenia Gravis Quality of Life 15-item revised scale (MG-QoL15r). Clinically meaningful improvement (CMI), minimal symptom expression (MSE), patient-acceptable symptom state (PASS), subdomain response, and corticosteroid sparing were evaluated.

RESULTS: Thirty-nine patients completed at least one treatment cycle, receiving a total of 210 cycles. In cycle 1, CMI rates were 89.7% for MG-ADL and 74.4% for QMG, with a median MG-ADL reduction of 4.0 points (p < 0.001); 69.2% achieved CMI after a single infusion. Composite PASS increased from 25.6% in cycle 1 to 54.5% in cycle 8. Subdomain analysis showed improvements across all domains for both the MG-ADL and the QMG, with the exception of QMG respiratory. Among patients on corticosteroids (n = 29), median prednisone dose decreased from 20.0 to 10.0 mg/day (p = 0.004), with 58.6% achieving reduction or discontinuation.

CONCLUSION: This first Eastern European real-world efgartigimod-treated cohort confirms rapid and sustained improvement and corticosteroid sparing, consistent with prior evidence.

PMID:42756311 | PMC:PMC13583037 | DOI:10.3389/fneur.2026.1945691


Source: https://pubmed.ncbi.nlm.nih.gov/4275631 ... 1&v=2.20.1
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