Sekimata Mao, Kinjo Yasuyuki, Tohyama Atsushi, Murakami Midori, Hashiwaki Sayumi, Saito Yuma, Higami Shota, Hagimoto Marina, Taketomi Ruka, Hoshino Kaori, Harada Hiroshi, Ueda Taeko, Kurita Tomoko, Matsuura Yusuke, Yoshino Kiyoshi
Department of Obstetrics and Gynecology, University of Occupational and Environmental Health, Kitakyushu, Fukuoka 807-8555, Japan.
Department of Nursing of Human Broad Development, University of Occupational and Environmental Health, Kitakyushu, Fukuoka 807-8555, Japan.
Oncol Lett. 2024 May 17;28(1):331. doi: 10.3892/ol.2024.14463. eCollection 2024 Jul.
Cytokine release syndrome (CRS) is a systemic inflammatory condition caused by an excessive immune response and cytokine overproduction. CRS is a life-threatening condition that is often associated with chimeric antigen receptor T-cell therapy. Despite the increased use of immune checkpoint inhibitors (ICIs), ICI-induced CRS remains rare. The present study describes a case of CRS that occurred after the administration of ICIs for recurrent adenocarcinoma of the uterine cervix. A 49-year-old woman received paclitaxel, carboplatin and pembrolizumab for recurrent cervical adenocarcinoma. On day 27 of the third cycle, the patient was admitted with a fever and suspected pyelonephritis. The following day, hypotension, upper respiratory symptoms and myalgia of the extremities were noted, and the left ventricular ejection fraction (LVEF) was decreased to 20%. Multiorgan failure (MOF) occurred, and the patient received ventilator support and continuous hemodiafiltration. Rhabdomyolysis, pancreatitis, erythema multiforme and enteritis were observed. CRS was diagnosed based on elevated ferritin and IL-6 levels. Steroid pulse therapy was administered; however, the MOF did not improve and the anti-IL-6-receptor monoclonal antibody tocilizumab (TOC) was administered. Subsequently, the LVEF improved to 50%, and the patient was removed from the ventilator on day 4 and from the continuous hemodiafiltration unit on day 6 after TOC administration. The patient was discharged on day 21. In conclusion, considering that ICI-induced CRS is a rare but severe complication, fever and other systemic conditions following ICI administration should be monitored.
细胞因子释放综合征(CRS)是一种由过度免疫反应和细胞因子过度产生引起的全身性炎症状态。CRS是一种危及生命的病症,常与嵌合抗原受体T细胞疗法相关。尽管免疫检查点抑制剂(ICI)的使用有所增加,但ICI诱导的CRS仍然罕见。本研究描述了一例在使用ICI治疗复发性子宫颈腺癌后发生CRS的病例。一名49岁女性因复发性宫颈腺癌接受了紫杉醇、卡铂和帕博利珠单抗治疗。在第三个周期的第27天,患者因发热和疑似肾盂肾炎入院。第二天,出现低血压、上呼吸道症状和四肢肌痛,左心室射血分数(LVEF)降至20%。发生了多器官功能衰竭(MOF),患者接受了呼吸机支持和持续血液透析滤过。观察到横纹肌溶解、胰腺炎、多形红斑和肠炎。根据铁蛋白和IL-6水平升高诊断为CRS。给予了类固醇冲击治疗;然而,MOF并未改善,随后给予了抗IL-6受体单克隆抗体托珠单抗(TOC)。随后,LVEF改善至50%,患者在给予TOC后的第4天脱离呼吸机,第6天脱离持续血液透析滤过装置。患者于第21天出院。总之,鉴于ICI诱导的CRS是一种罕见但严重的并发症,应监测ICI给药后的发热和其他全身状况。