Jamison Kiara, Medepalli Lalitha C, Ye Star
Internal Medicine, Northside Hospital Gwinnett, Lawrenceville, USA.
Cardiology/Cardiooncology, Northside Cardiovascular Institute (NCVI) Northside Hospital, Atlanta, USA.
Cureus. 2024 May 13;16(5):e60184. doi: 10.7759/cureus.60184. eCollection 2024 May.
Immune checkpoint inhibitors (ICIs) are a form of immunotherapy increasingly utilized in cancer therapies. While offering promise in malignancy treatment, ICIs, including atezolizumab, can elicit immune-related adverse events (irAEs) such as cardiotoxicity. We present the case of a 67-year-old male with stage IV metastatic small-cell lung cancer undergoing carboplatin, etoposide, and atezolizumab therapy, who developed pericardial tamponade two months into treatment. Initially presenting with hypoxia on day three of his third treatment cycle, he was admitted due to multifocal pneumonia and subsequently diagnosed with pericardial tamponade stemming from a sizable pericardial effusion. Pericardiocentesis was performed, effectively resolving the tamponade. Infectious etiology was ruled out. Notably, there was no associated myocarditis, as evidenced by negative cardiac markers and magnetic resonance imaging (MRI) findings, and cytologic analysis of the pericardial fluid did not reveal malignant cells, indicating an isolated immunologic etiology for the pericardial effusion. Following successful management, including oxygen support and a prednisone taper, chemotherapy without immunotherapy was resumed after a one-week delay. This rare case underscores the significance of promptly utilizing multimodality imaging with timely cardiology intervention, a prompt pericardial fluid analysis in diagnosing cardiac irAEs, and management leading to improved patient outcomes.
免疫检查点抑制剂(ICIs)是一种在癌症治疗中越来越常用的免疫疗法。虽然ICIs在恶性肿瘤治疗中带来了希望,但包括阿替利珠单抗在内的ICIs可引发免疫相关不良事件(irAEs),如心脏毒性。我们报告了一例67岁男性IV期转移性小细胞肺癌患者,接受卡铂、依托泊苷和阿替利珠单抗治疗,在治疗两个月后出现心包填塞。在他第三个治疗周期的第三天最初表现为缺氧,因多灶性肺炎入院,随后被诊断为心包填塞,由大量心包积液引起。进行了心包穿刺术,有效解除了填塞。排除了感染性病因。值得注意的是,没有相关心肌炎,心脏标志物和磁共振成像(MRI)结果均为阴性证明了这一点,心包液的细胞学分析未发现恶性细胞,表明心包积液为孤立的免疫性病因。在成功处理后,包括氧疗支持和逐渐减量使用泼尼松,在延迟一周后恢复了无免疫治疗的化疗。这个罕见病例强调了及时采用多模态成像并及时进行心脏科干预、及时进行心包液分析以诊断心脏irAEs以及进行管理以改善患者预后的重要性。