尼妥珠单抗诱发的心肌炎的临床特征、诊断和处理。

IF 3 3区 医学 Q2 ONCOLOGY
Investigational New Drugs Pub Date : 2024-02-01 Epub Date: 2024-01-23 DOI:10.1007/s10637-024-01421-7
Meng-Ting Li, Yang He, Si-Yong Huang, Xiao Hu, Ji-Sheng Chen
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引用次数: 0

摘要

尼妥珠单抗可导致致命性心肌炎。我们旨在分析尼妥珠单抗诱发心肌炎的临床特征,为临床诊断、治疗和预防提供证据。我们在电子数据库中找到了2000年至2023年涉及尼妥珠单抗诱发心肌炎的研究,并进行了回顾性分析。共纳入 66 例患者,中位年龄为 68 岁。心肌炎的中位发病时间为 11.5 天。心肌炎患者的主要受累器官是心脏(100.0%)和骨骼肌(22.7%)。主要临床表现为呼吸困难(49.2%)、乏力(47.6%)和肌痛(25.4%)。肌钙蛋白、肌钙蛋白 T、肌钙蛋白 I、肌酸激酶、肌酸激酶心肌带、肌酸磷酸激酶、C 反应蛋白、脑钠肽和 N 端脑钠肽前体的水平显著升高。组织病理学通常显示淋巴细胞浸润、心肌坏死和纤维化。心肌免疫参数通常呈阳性。心脏造影通常提示完全性心脏传导阻滞、室内传导延迟、心律失常、心肌梗死、水肿、左室射血分数降低、心室功能障碍以及其他心肌炎症状。42名患者(63.6%)在停用尼妥珠单抗并接受全身皮质类固醇、免疫球蛋白、浆细胞吸出术和免疫抑制剂治疗后的中位时间为8天,病情得到缓解。35名患者最终死于心肌炎(68.6%)、癌症(20.0%)、呼吸衰竭(5.7%)和其他原因(5.7%)。尼妥珠单抗诱发的心肌炎应根据临床症状、组织病理学表现、免疫学参数和心功能影像学检查进行综合诊断。应立即停用 Nivolumab,浆细胞清除术和全身皮质类固醇联合免疫球蛋白或免疫抑制剂可能是一种有效的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical characteristics, diagnosis and management of nivolumab-induced myocarditis.

Nivolumab can cause fatal myocarditis. We aimed to analyze the clinical characteristics of nivolumab-induced myocarditis and provide evidence for clinical diagnosis, treatment, and prevention. Studies involving nivolumab-induced myocarditis were identified in electronic databases from 2000 to 2023 for retrospective analysis. A total of 66 patients were included, with a median age of 68 years. The median onset time of myocarditis is 11.5 days. The main organs affected in persons presented with myocarditis are heart (100.0%) and skeletal muscle (22.7%). The main clinical manifestations are dyspnea (49.2%), fatigue (47.6%), and myalgias (25.4%). The levels of troponin, troponin T, troponin I, creatine kinase, creatine kinase myocardial band, creatine phosphokinase, C-reactive protein, brain natriuretic peptide, and N-terminal brain natriuretic peptide precursor were significantly increased. Histopathology often shows lymphocyte infiltration, myocardial necrosis, and fibrosis. Myocardial immunological parameters usually present positive. Cardiac imaging often suggests complete heart block, intraventricular conduction delay, arrhythmia, myocardial infarction, edema, left ventricular ejection fractions reduction, ventricular dysfunction, and other symptoms of myocarditis. Forty-two (63.6%) patients achieved remission within a median time of 8 days after discontinuation of nivolumab and treatment with systemic corticosteroids, immunoglobulins, plasmapheresis, and immunosuppressant. Thirty-five patients eventually died attributed to myocarditis (68.6%), cancer (20.0%), respiratory failure (5.7%), and other reasons (5.7%). Nivolumab-induced myocarditis should be comprehensively diagnosed based on clinical symptoms, histopathological manifestations, immunological parameters, and cardiac function imaging examinations. Nivolumab should be discontinued immediately, plasmapheresis and systemic corticosteroids combined with immunoglobulins or immunosuppressants may be an effective treatment.

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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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