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Immune Checkpoint Inhibition-Related Myasthenia-Myositis-Myocarditis Responsive to Complement Blockade
Christopher Nelke1, Marc Pawlitzki1, Ruth Kerkhoff1
1From the Department of Neurology (C.N., M.P., R.K., C.B.S., O.A., S.G.M., T.R.); Institute of Neuropathology (E.N.-J.); and Division of Cardiology, Pulmonology, and Vascular Medicine (A.P.), Medical Faculty, Heinrich Heine University Dusseldorf, Germany.
Immune checkpoint inhibitors can cause severe neuromuscular immune-related adverse events (irAEs). Early muscle biopsy identified a treatment target, leading to rapid improvement in a patient with myasthenia-myositis-myocarditis overlap.
Area of Science:
- Oncology
- Immunology
- Neurology
Background:
- Immune checkpoint inhibitors (ICIs) offer significant cancer treatment benefits but can induce immune-related adverse events (irAEs).
- Neuromuscular irAEs, such as myositis and myasthenia gravis (MG), present serious challenges due to high morbidity and mortality.
Observation:
- A 47-year-old woman with breast cancer developed severe tetraparesis, dysphagia, and myalgia during ICI therapy.
- The patient had a prior diagnosis of MG with thymoma, presenting as a myasthenia-myositis-myocarditis overlap syndrome.
Findings:
- Despite ICI discontinuation and standard treatments, the patient showed no clinical response.
- A muscle biopsy revealed complement deposition, guiding the use of eculizumab.
- Eculizumab therapy resulted in prompt improvement of muscle strength and cardiac function.
Implications:
- Early diagnosis and targeted therapy, guided by muscle biopsy, are crucial for managing refractory neuromuscular irAEs.
- Identifying specific treatment targets, like complement deposition, can overcome limitations of standard approaches.
- Further research into patient-tailored strategies is essential to improve outcomes for neuromuscular irAEs.
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