研究动态
Articles below are published ahead of final publication in an issue. Please cite articles in the following format: authors, (year), title, journal, DOI.

免疫检查点抑制剂治疗宫颈癌复发引起的细胞因子释放综合征:病例报告。

Cytokine release syndrome induced by immune checkpoint inhibitor treatment for uterine cervical cancer recurrence: A case report.

发表日期:2024 Jul
作者: Mao Sekimata, Yasuyuki Kinjo, Atsushi Tohyama, Midori Murakami, Sayumi Hashiwaki, Yuma Saito, Shota Higami, Marina Hagimoto, Ruka Taketomi, Kaori Hoshino, Hiroshi Harada, Taeko Ueda, Tomoko Kurita, Yusuke Matsuura, Kiyoshi Yoshino
来源: CYTOKINE & GROWTH FACTOR REVIEWS

摘要:

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量产生引起的全身炎症性疾病。 CRS 是一种危及生命的疾病,通常与嵌合抗原受体 T 细胞疗法相关。尽管免疫检查点抑制剂 (ICIs) 的使用越来越多,但 ICI 诱发的 CRS 仍然很少见。本研究描述了一例因宫颈复发腺癌使用 ICI 后发生的 CRS 病例。一名 49 岁女性因复发性宫颈腺癌接受紫杉醇、卡铂和派姆单抗治疗。第三周期第27天,患者因发烧并疑似肾盂肾炎入院。次日出现低血压、上呼吸道症状和四肢肌痛,左心室射血分数(LVEF)降至20%。发生多器官衰竭(MOF),患者接受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。 CRS 的诊断依据是铁蛋白和 IL-6 水平升高。进行类固醇冲击治疗;然而,MOF 没有改善,并给予了抗 IL-6 受体单克隆抗体托珠单抗 (TOC)。随后,LVEF 改善至 50%,TOC 给药后,患者在第 4 天脱离呼吸机,并在第 6 天脱离连续血液透析滤过装置。患者于第 21 天出院。 总之,考虑到 ICI 引起的 CRS 是一种罕见但严重的并发症,应监测 ICI 给药后的发烧和其他全身状况。版权所有:© 2024 Sekimata 等人。
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.Copyright: © 2024 Sekimata et al.