当免疫疗法打击心脏:免疫检查点抑制剂诱导心肌炎的多模式方法:一个病例系列和文献综述

Ahmed Basuoni , Marwa Makhlouf , Waleed Dawelbeit , Donia Ahmed , Hadil Al-Sharqi , Suhaila Al Farsi , Khalid Al-Baimani
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引用次数: 0

摘要

免疫检查点抑制剂(ICI)的使用与包括心肌炎在内的潜在危及生命的心血管并发症相关。本病例系列旨在评估ici诱导心肌炎的不同治疗方法和结果,并与国际基准进行比较回顾。方法回顾性分析苏丹卡布斯综合癌症护理与研究中心(SQCCCRC)诊断为ici性心肌炎的患者。ici性心肌炎的诊断是基于临床表现、心脏生物标志物和排除其他鉴别诊断后的心脏影像学。治疗策略包括皮质类固醇和免疫抑制治疗。对临床结果和死亡率进行纵向监测,并与国际基准文献综述进行比较。结果2年内共发现6例心肌炎,心肌炎患病率为1.8 %。心肌炎可发生在第1 - 9个周期之间的任何时间,临床表现从轻微症状到严重症状,包括中风、类固醇抵抗和心源性休克。采用多模态成像,特别是心脏磁共振;主要治疗包括皮质类固醇,一个难治性病例需要霉酚酸酯(MMF)。5例患者完全康复。结论本研究结果表明,在许多癌症中心,由于诊断不足和缺乏风险分层方案,ici诱导的心肌炎发病率可能被低估。对于非暴发性或I/II级病例的治疗,应考虑口服类固醇,而类固醇耐药性可能需要替代免疫抑制治疗。多学科小组讨论对于评估可能病例中ICI治疗的继续是必要的。加强早期发现和及时开始类固醇治疗的方案改善了结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
When immunotherapy strikes the heart: A multimodal approach to immune checkpoint inhibitors induced myocarditis: A case series and literature review

Background

Immune checkpoint inhibitors (ICI) use is associated with potentially life-threatening cardiovascular complication including myocarditis. This case series aims to evaluate the different management approaches and outcomes of ICI-induced myocarditis with a comparative review with international benchmarks.

Methods

This retrospective case series analyzed patients diagnosed with ICI-induced myocarditis at Sultan Qaboos Comprehensive Cancer Care and Research Center (SQCCCRC). The diagnosis of ICI-induced myocarditis was based on clinical presentation, cardiac biomarkers, and cardiac imaging after the exclusion of other differential diagnoses. Management strategies included corticosteroids and immunosuppressive therapy. Clinical outcomes and mortality were monitored longitudinally compared with a literature review of international benchmarks.

Results

A total of 6 cases were identified over 2 years, with a myocarditis prevalence of 1.8 %. Myocarditis onset occurred anytime between the first and the ninth cycle, with clinical presentations varying from mild symptoms to severe presentations with stroke, steroid resistance, and cardiogenic shock. Multimodality imaging, particularly cardiac magnetic resonance, was utilized; the mainstay therapy included corticosteroids, with one refractory case requiring mycophenolate mofetil (MMF). Complete recovery occurred in five patients.

Conclusion

The study outcome showed that the incidence of ICI-induced myocarditis may be under-reported due to underdiagnosis and the absence of risk stratification protocols in many cancer centers. For treatment of non-fulminant or Grade I/II cases, oral steroids should be considered, while steroid resistance may necessitate alternative immunosuppressive therapies. Multidisciplinary team discussions are essential to assess the continuation of ICI therapy in possible cases. Protocols enhancing early detection and timely steroid therapy initiation improve outcomes.
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