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Efgartigimod improved MG-ADL and QMG scores in 81 Chinese patients with generalized myasthenia gravis.

Efgartigimod improved MG-ADL and QMG scores in 81 Chinese patients with generalized myasthenia gravi…
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Key Takeaway
Consider efgartigimod for acute control in gMG, noting reduced-frequency regimens may be feasible in selected cases.

This single-center, retrospective analysis included 81 Chinese patients with generalized myasthenia gravis (gMG). Patients received efgartigimod at 10 mg/kg weekly for 4 weeks, with retreatment and regimen modifications allowed in selected cases. Follow-up assessments occurred at week 2 and week 4.

Primary outcomes were defined as an MG-ADL reduction ≥2 and a QMG reduction ≥3. After the first cycle, 65 patients (80.25%) achieved the MG-ADL response, and 63 patients (77.78%) achieved the QMG response. Among 41 patients (63.07%) who received only one cycle, disease control was maintained with concomitant immunosuppressive therapies without requiring additional efgartigimod.

Sixteen patients received multiple cycles (≥2) and showed progressive improvement with flexible retreatment. Nine patients received a reduced-frequency regimen of 2 infusions every 2 weeks, which maintained efficacy while reducing infusion burden. Safety data indicated adverse events were mostly mild, no serious adverse events were reported, and no new safety signals were observed.

The study supports an induction-maintenance strategy using efgartigimod for acute control and conventional immunosuppressants for long-term management. However, because this was a retrospective analysis, causal conclusions cannot be drawn, and the results may not be generalizable to other populations.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
ObjectiveThis study aimed to evaluate the real-world efficacy, safety, and application patterns of efgartigimod in Chinese patients with generalized myasthenia gravis (gMG), with a focus on individualized treatment strategies.MethodsWe conducted a single-center, retrospective analysis of 81 gMG patients who received at least one standard cycle of efgartigimod (10 mg/kg weekly for 4 weeks). Disease severity was assessed using Myasthenia Gravis Activities of Daily Living (MG-ADL), Quantitative Myasthenia Gravis (QMG), and Myasthenia Gravis Composite (MGC) scores at baseline, week 2, and week 4. Retreatment and regimen modifications were individualized, which included exploration of a reduced-frequency regimen (2 infusions every 2 weeks) in selected patients.ResultsIn the overall cohort, 65 (80.25%) and 63 (77.78%) patients achieved MG-ADL (reduction ≥2) and QMG (reduction ≥3) responses, respectively, after the first cycle. 65 (80.25%) patients received only one cycle; among them, 41 (63.07%) maintained disease control with concomitant immunosuppressive therapies without requiring additional efgartigimod. The 16 patients receiving multiple cycles (≥2) had higher baseline disease severity (higher Myasthenia Gravis Foundation of America class, MG-ADL, and QMG scores) and showed progressive improvement with flexible retreatment. In a selected subgroup of 9 patients (based on age, robust response, and significant IgG reduction), a reduced-frequency regimen (2 infusions every 2 weeks) maintained efficacy while reducing the infusion burden. Adverse events were mostly mild, with no new safety signals.InterpretationEfgartigimod demonstrated rapid and broad efficacy in a real-world gMG cohort. An “induction-maintenance” strategy, using efgartigimod for acute control and conventional immunosuppressants for long-term management, proved effective in most patients. A reduced-frequency regimen may be feasible in selected cases, highlighting the value of individualized treatment approaches in optimizing outcomes and reducing treatment burden.
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