Immune Checkpoint Inhibition–Related Myasthenia-Myositis-Myocarditis Responsive to Complement Blockade

肌炎 重症肌无力 封锁 心肌炎 医学 免疫学 补语(音乐) 免疫检查点 免疫系统 免疫疗法 内科学 生物 受体 生物化学 互补 基因 表型
作者
Christopher Nelke,Marc Pawlitzki,Ruth Kerkhoff,Christina B. Schroeter,Orhan Aktaş,Eva Neuen-Jacob,Amin Polzin,Sven G. Meuth,Tobias Ruck
出处
期刊:Neuroimmunology and Neuroinflammation [Ovid Technologies (Wolters Kluwer)]
卷期号:11 (1) 被引量:1
标识
DOI:10.1212/nxi.0000000000200177
摘要

ObjectiveImmune checkpoint inhibitors (ICIs) have revolutionized cancer therapy but come with immune-related adverse events (irAEs) that provide a novel challenge for treating physicians. Neuromuscular irAEs, including myositis, myasthenia gravis (MG), and demyelinating polyradiculoneuropathy, lead to significant morbidity and mortality.MethodsWe present a case of severe myasthenia-myositis-myocarditis overlap in a patient receiving ICIs for breast cancer. Clinical findings were recorded.ResultsA 47-year-old woman developed tetraparesis, dysphagia, and muscle pain during ICI treatment. MG with a thymoma had been diagnosed earlier. Neuromuscular overlap irAEs with cardiac affection was confirmed, and ICI treatment was discontinued. Given a lack of clinical response to standard therapies, a muscle biopsy was performed demonstrating complement deposition. Eculizumab treatment led to rapid improvement in muscle strength and cardiac function.DiscussionNeuromuscular irAEs are associated with a high in-hospital mortality, and specific treatment strategies remain an unmet need. Here, early muscle biopsy enabled targeted therapy after standard approaches failed, thereby highlighting the value of identifying a specific treatment target. To improve therapeutic outcomes, the development of patient-tailored strategies for neuromuscular irAEs requires further studies.
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