免疫检查点抑制剂和嵌合抗原受体T细胞疗法中的心脏毒性及围手术期注意事项:一项叙述性综述

Cardiotoxicity and peri-operative considerations in immune checkpoint inhibitor and chimeric antigen receptor T-cell therapy: a narrative review.

作者信息

Malode Aishwarya, Makwana Bhargav, Patel Vahin, Khadke Sumanth, Parikh Aneri, Bagga Arindam, Dani Sourbha, Ganatra Sarju

机构信息

Department of Cardiovascular Medicine, Department of Medicine, Lahey Hospital and Medical Center, Burlington, MA, USA.

出版信息

Anaesthesia. 2025 Feb;80 Suppl 2:25-37. doi: 10.1111/anae.16493. Epub 2025 Jan 8.

Abstract

INTRODUCTION

Immunotherapy has transformed cancer treatment, particularly with immune checkpoint inhibitors and chimeric antigen receptor T-cell therapy. Despite their efficacy, these therapies can induce cardiotoxicity, presenting significant clinical challenges. Immune checkpoint inhibitors can cause myocarditis; pericarditis; arrhythmias; and myocardial infarction through immune-mediated inflammation. Chimeric antigen receptor T-cell therapy may result in cardiovascular complications due to cytokine release syndrome, including myocardial dysfunction, endothelial damage and arrhythmias.

METHODS

We used PubMed, Embase and Google Scholar to search for peer-reviewed articles in September 2024 without setting any date limits. Our selection criteria encompassed studies focusing on cardiotoxicity related to immune checkpoint inhibitors or chimeric antigen receptor T-cell therapy, comprising original research, meta-analyses, clinical trials and review articles. The findings were reported narratively.

RESULTS

Early diagnosis of cardiotoxicity is critical but challenging due to non-specific symptoms. Diagnostic tools include ECG; cardiac biomarkers; echocardiography; cardiac magnetic resonance imaging; and endomyocardial biopsy. However, no single tool is definitive. High-dose corticosteroids are the first-line treatment for immune checkpoint inhibitor-induced myocarditis, with additional immunosuppressive therapies for refractory cases. Standard heart failure management protocols should be followed in cases of heart failure. Tocilizumab and corticosteroids are utilised for chimeric antigen receptor T-cell therapy-induced cytokine release syndrome, alongside supportive care, including fluid resuscitation and vasopressors for severe cases.

DISCUSSION

As the use of immunotherapy expands, understanding the mechanisms, risk factors and management strategies for cardiotoxicity is increasingly important. Collaborative efforts among oncologists, cardiologists and anaesthetists are essential to mitigate these risks, especially in peri-operative settings. Ongoing research is vital to improve the safe and effective use of immunotherapeutic drugs while minimising cardiovascular adverse effects.

摘要

引言

免疫疗法已经改变了癌症治疗方式,尤其是免疫检查点抑制剂和嵌合抗原受体T细胞疗法。尽管这些疗法疗效显著,但它们会诱发心脏毒性,带来重大的临床挑战。免疫检查点抑制剂可通过免疫介导的炎症引发心肌炎、心包炎、心律失常和心肌梗死。嵌合抗原受体T细胞疗法可能因细胞因子释放综合征导致心血管并发症,包括心肌功能障碍、内皮损伤和心律失常。

方法

我们于2024年9月使用PubMed、Embase和谷歌学术搜索同行评议文章,不设任何日期限制。我们的选择标准包括聚焦于与免疫检查点抑制剂或嵌合抗原受体T细胞疗法相关的心脏毒性的研究,包括原创研究、荟萃分析、临床试验和综述文章。研究结果采用叙述性报告。

结果

心脏毒性的早期诊断至关重要,但由于症状不具特异性而具有挑战性。诊断工具包括心电图、心脏生物标志物、超声心动图、心脏磁共振成像和心内膜心肌活检。然而,没有单一工具是决定性的。大剂量皮质类固醇是免疫检查点抑制剂诱发心肌炎的一线治疗药物,难治性病例需额外的免疫抑制疗法。心力衰竭病例应遵循标准的心力衰竭管理方案。托珠单抗和皮质类固醇用于治疗嵌合抗原受体T细胞疗法诱发的细胞因子释放综合征,同时给予支持治疗,包括严重病例的液体复苏和血管加压药。

讨论

随着免疫疗法的应用不断扩大,了解心脏毒性的机制、危险因素和管理策略变得越来越重要。肿瘤学家、心脏病学家和麻醉师之间的合作对于降低这些风险至关重要,尤其是在围手术期。持续的研究对于提高免疫治疗药物的安全有效使用,同时将心血管不良反应降至最低至关重要。

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