Department of Internal Medicine, Kaiser Permanente San Francisco Medical Center, San Francisco, CA.
Department of Cardiology, Kaiser Permanente San Francisco Medical Center, San Francisco, CA.
Perm J. 2020 Dec;24:1. doi: 10.7812/TPP/20.037.
Immune checkpoint inhibitors (ICI) have led to improved survival in patients with a number of different tumor types. The ICI agent nivolumab induces anti-tumor immune responses by inhibiting the programmed cell death 1 protein, but side effects include cardiac immune-related adverse events (irAE) such as myocarditis.¹ The association of nivolumab with atherosclerotic disease has been rarely reported.
A 62-year-old man with metastatic melanoma and recent myocardial infarction (MI) presented with recurrent MI after having undergone several cycles of nivolumab therapy. Repeat cardiac catheterization revealed rapidly progressive in-stent restenosis and diffuse coronary artery disease (CAD) requiring bypass surgery and warranting cessation of nivolumab therapy.
Nivolumab has been linked with dysregulation of immune responses including enhanced T cell activity, which is implicated in CAD. The timing of nivolumab therapy and presentation with non ST elevation myocardial infarction in this patient suggests a serious T cell-driven medication adverse effect. Therefore, close monitoring for atherosclerotic disease progression is warranted in patients on immunotherapy.
免疫检查点抑制剂(ICI)已使多种不同肿瘤类型的患者的生存率得到提高。ICI 药物纳武利尤单抗通过抑制程序性细胞死亡 1 蛋白诱导抗肿瘤免疫反应,但副作用包括心肌炎等心脏免疫相关不良事件(irAE)。¹纳武利尤单抗与动脉粥样硬化疾病的关联很少有报道。
一名 62 岁男性患有转移性黑色素瘤和近期心肌梗死(MI),在接受几轮纳武利尤单抗治疗后再次发生 MI。重复的心脏导管检查显示支架内再狭窄迅速进展和弥漫性冠状动脉疾病(CAD),需要旁路手术,并需要停止纳武利尤单抗治疗。
纳武利尤单抗与免疫反应失调有关,包括增强的 T 细胞活性,这与 CAD 有关。该患者纳武利尤单抗治疗时机和非 ST 段抬高型心肌梗死的表现提示存在严重的 T 细胞驱动的药物不良反应。因此,免疫治疗患者需要密切监测动脉粥样硬化疾病进展。