Immune checkpoint inhibitor-induced myocarditis and multiple adverse events with pre-existing rheumatoid arthritis: a case report and literature review.

IF 2.9 Q3 IMMUNOLOGY
Shion Kachi, Mirei Shirakashi, Takashi Nomizo, Mei Onishi, Eri Toda Kato, Tomomi W Nobashi, Hideo Onizawa, Ryosuke Hiwa, Hideaki Tsuji, Shuji Akizuki, Ran Nakashima, Akira Onishi, Hajime Yoshifuji, Masao Tanaka, Kosaku Murakami, Akio Morinobu
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Abstract

Immune checkpoint inhibitors (ICIs) can trigger immune-related adverse events (irAEs) and rheumatoid arthritis (RA) reactivation in cancer patients with pre-existing RA. Studies indicate RA reactivation occurs in approximately 50% of these patients, while new irAEs develop in 25-50% of ICI-treated patients. Furthermore, ICI-induced myocarditis has been reported to have a high mortality rate, ranging from 25% to 50%. No prior reports have detailed the clinical course of ICI-induced myocarditis in patients with RA. We describe a 77-year-old man with RA who developed myocarditis, myositis, and RA flare following treatment with the PD-LI inhibitor, atezolizumab, for small-cell lung cancer. High-dose glucocorticoid (GC) therapy and intravenous immunoglobulin improved myocarditis and myositis. Corticosteroid tapering led to organizing pneumonia, necessitating a dosage adjustment. Once resolved, tapering resumed. During irAEs treatment, the patient maintained a partial response without cancer recurrence for ten months, and required no further cancer-specific therapy. To our knowledge, this is the first detailed report of ICI-induced myocarditis in a patient with pre-existing RA. Our findings emphasize the importance of vigilant monitoring of both irAEs and RA disease activity for optimal patient management.

免疫检查点抑制剂诱导的心肌炎和多重不良事件与预先存在的类风湿关节炎:1例报告和文献复习。
免疫检查点抑制剂(ICIs)可引发免疫相关不良事件(irAEs)和类风湿关节炎(RA)的再激活。研究表明,大约50%的患者会出现RA再激活,而在接受ici治疗的患者中,25-50%会出现新的RA。此外,据报道,ici诱发的心肌炎死亡率很高,从25%到50%不等。没有先前的报道详细的临床过程的ici诱导心肌炎患者RA。我们描述了一位77岁的RA患者,他在接受PD-LI抑制剂atezolizumab治疗小细胞肺癌后出现心肌炎、肌炎和RA发作。大剂量糖皮质激素(GC)治疗和静脉注射免疫球蛋白可改善心肌炎和肌炎。皮质类固醇逐渐减少导致组织性肺炎,需要调整剂量。一旦问题得到解决,就继续缩减规模。在irAEs治疗期间,患者在10个月内保持了部分反应,没有癌症复发,并且不需要进一步的癌症特异性治疗。据我们所知,这是第一个详细的报告,ici诱发心肌炎患者已有RA。我们的研究结果强调了警惕监测RA和RA疾病活动性对最佳患者管理的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Immunological Medicine
Immunological Medicine Medicine-Immunology and Allergy
CiteScore
7.10
自引率
2.30%
发文量
19
审稿时长
19 weeks
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