检查点抑制的可怕三合一:1例转移性皮肤鳞状细胞癌患者由西米单抗诱发重症肌无力、心肌炎和肌炎的报告。

Pub Date : 2020-07-04 eCollection Date: 2020-01-01 DOI:10.1155/2020/5126717
Nikeshan Jeyakumar, Mikel Etchegaray, Jason Henry, Laura Lelenwa, Bihong Zhao, Ana Segura, L Maximilian Buja
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引用次数: 33

摘要

背景:我们报告了一例鳞状细胞癌(SCC)患者在接受抗pd -1免疫检查点抑制剂(ICI)塞米单抗后出现重症肌无力(MG)、肌炎和心肌炎。案例演示。一名86岁男性转移性眼周SCC患者在接受西米单抗治疗3周后表现为左眼视力下降、严重疲劳、下背部和双侧髋关节疼痛。几小时内,他出现发音困难、咽分泌物和吞咽困难,需要插管。心肌内膜活检显示活跃的淋巴细胞介导的坏死与ici诱导的心肌炎一致。抗横纹肌和抗乙酰胆碱受体抗体升高,与肌炎和重症肌无力一致。尽管接受了血浆交换治疗、类固醇和静脉注射免疫球蛋白,他还是死于心脏骤停。结论:重症肌无力、心肌炎或肌炎的存在应提示评估所有三种毒性,因为它们可能代表重叠综合征。这些免疫毒性的严重程度突出了临床医生怀疑ICIs多重同时不良反应的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Terrible Triad of Checkpoint Inhibition: A Case Report of Myasthenia Gravis, Myocarditis, and Myositis Induced by Cemiplimab in a Patient with Metastatic Cutaneous Squamous Cell Carcinoma.

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The Terrible Triad of Checkpoint Inhibition: A Case Report of Myasthenia Gravis, Myocarditis, and Myositis Induced by Cemiplimab in a Patient with Metastatic Cutaneous Squamous Cell Carcinoma.

Background: We report a case of a patient with squamous cell carcinoma (SCC) who developed myasthenia gravis (MG), myositis, and myocarditis after receiving cemiplimab, an anti-PD-1 immune checkpoint inhibitor (ICI). Case Presentation. An 86-year-old man with metastatic periocular SCC presented with decreased vision in the left eye, severe fatigue, and lower back and bilateral hip pain 3 weeks after receiving cemiplimab. Within hours, he developed dysphonia, pharyngeal secretions, and dysphagia, necessitating intubation. Endomyocardial biopsy revealed active lymphocyte-mediated necrosis consistent with ICI-induced myocarditis. Anti-striated muscle and anti-acetylcholine receptor antibodies were elevated, consistent with myositis and myasthenia gravis. Despite plasma exchange therapy, steroids, and intravenous immunoglobulin, he died from cardiac arrest.

Conclusions: The presence of myasthenia gravis, myocarditis, or myositis should prompt evaluation for all three toxicities as they may represent an overlap syndrome. The severity of these immunotoxicities highlights the need for clinicians to suspect multiple simultaneous adverse effects of ICIs.

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