Brazel Danielle, Lee Seungshin, Mahadevan Aditya, Warnecke Brian, Parajuli Ritesh
Department of Medicine, University of California Irvine Medical Center, Orange, USA.
Department of Hematology and Oncology, University of California Irvine School of Medicine, Orange, USA.
Cureus. 2023 Jul 12;15(7):e41781. doi: 10.7759/cureus.41781. eCollection 2023 Jul.
Immune checkpoint inhibitors (ICIs) as standard of care have revolutionized the treatment of patients with metastatic melanoma. The combination of nivolumab and ipilimumab improves treatment efficacy and prolongs survival compared to monotherapy alone. However, combination therapy is also associated with an increased incidence of adverse events. We report an uncommon yet important case of multi-organ failure in a patient following a single dose of nivolumab plus ipilimumab. A 60-year-old male with a history of ulcerative colitis in remission and metastatic melanoma was admitted on February 25, 2021, for presumed sepsis, after presenting with neutropenic fever. His brain metastases were previously resected on January 14, 2021, and he was started on dexamethasone 4 mg BID for six weeks. On February 11, 2021, he received one dose of nivolumab plus ipilimumab, per the CheckMate-067 protocol. He presented 14 days later with fever, diarrhea, pancytopenia, renal failure, drug-induced hepatitis, and myocarditis. The infectious workup was negative. His neutropenia responded to growth factors. He was diagnosed with interstitial nephritis due to immunotherapy and treated with corticosteroids. His symptoms resolved with concomitant improvement of his renal, hepatic, and cardiac function. He was discharged home in a stable condition. Although these specific immune-related adverse events (irAEs) are uncommon and rarely occur simultaneously, ICIs can trigger non-specific immune system activation, resulting in widespread inflammatory effects. Since irAEs can lead to multi-organ failure, as evidenced in this case, early recognition and institution of high-dose steroids are critical to preventing rapid deterioration. Given that ICI therapy is the standard of care for several cancers and is often studied in clinical trials, increased education on irAE toxicity and updated algorithms on the management of febrile cancer patients are warranted.
免疫检查点抑制剂(ICIs)作为标准治疗方案,彻底改变了转移性黑色素瘤患者的治疗方式。与单药治疗相比,纳武单抗和伊匹单抗联合使用可提高治疗效果并延长生存期。然而,联合治疗也会增加不良事件的发生率。我们报告了一例在接受单剂量纳武单抗加伊匹单抗治疗后发生多器官衰竭的罕见但重要的病例。一名60岁男性,有溃疡性结肠炎缓解病史和转移性黑色素瘤,因中性粒细胞减少性发热伴疑似脓毒症于2021年2月25日入院。他的脑转移瘤此前于2021年1月14日切除,开始服用地塞米松4毫克,每日两次,共六周。2021年2月11日,他按照CheckMate - 067方案接受了一剂纳武单抗加伊匹单抗治疗。14天后,他出现发热、腹泻、全血细胞减少、肾衰竭、药物性肝炎和心肌炎。感染相关检查结果为阴性。他的中性粒细胞减少对生长因子有反应。他被诊断为免疫治疗引起的间质性肾炎,并接受了皮质类固醇治疗。随着肾功能、肝功能和心功能的改善,他的症状也得到缓解。他出院时情况稳定。尽管这些特定的免疫相关不良事件(irAEs)并不常见,且很少同时发生,但ICIs可引发非特异性免疫系统激活,导致广泛的炎症反应。正如本病例所示,由于irAEs可导致多器官衰竭,早期识别并给予大剂量类固醇治疗对于防止病情迅速恶化至关重要。鉴于ICI治疗是几种癌症的标准治疗方案,且经常在临床试验中进行研究,有必要加强对irAE毒性的教育,并更新发热癌症患者管理的算法。