Sun Maoben, Xu Guihua, Cai Liangzhen, He Shaozhong
Department of Oncology, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523000, P.R. China.
Dongguan Key Laboratory of Precision Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, Guangdong 523000, P.R. China.
Oncol Lett. 2024 Jul 23;28(4):452. doi: 10.3892/ol.2024.14586. eCollection 2024 Oct.
Although the efficacy of treatment strategies for cancer have been improving steadily over the past decade, the adverse event profile following such treatments has also become increasingly complex. The present report described the case of a 67-year-old male patient with gastric stump carcinoma with liver invasion. The patient was treated with oxaliplatin and capecitabine (CAPEOX regimen) chemotherapy, combined with the programmed cell death protein-1 (PD-1) inhibitor tislelizumab. Following treatment, the patient suffered from chills, high fever and facial flushing, followed by shock. Relevant examination results revealed severe multiple organ damage, as well as a significant elevation in IL-6 and procalcitonin (PCT) levels. Initially, the patient was diagnosed with either immune-related adverse events (irAEs) associated with cytokine release syndrome caused by tislelizumab or severe bacterial infection. However, when tislelizumab treatment was stopped and the CAPEOX chemotherapy regimen was reapplied, similar symptoms recurred. Following screening, it was finally determined that severe hypersensitivity reaction (HSR) caused by oxaliplatin was the cause underlying these symptoms. A literature review was then performed, which found that severe oxaliplatin-related HSR is rare, rendering the present case atypical. The present case exhibited no common HSR symptoms, such as cutaneous and respiratory symptoms. However, the patient suffered from serious multiple organ damage, which was misdiagnosed as irAE when oxaliplatin chemotherapy combined with the PD-1 inhibitor was administered. In addition, this apparent severe oxaliplatin-related HSR caused a significant increase in PCT levels, which was misdiagnosed as severe bacterial infection and prevented the use of glucocorticoids. This, in turn, aggravated the damage in this patient.
尽管在过去十年中癌症治疗策略的疗效一直在稳步提高,但这些治疗后的不良事件谱也变得越来越复杂。本报告描述了一名67岁男性胃残端癌伴肝转移患者的病例。该患者接受了奥沙利铂和卡培他滨(CAPEOX方案)化疗,并联合程序性细胞死亡蛋白1(PD-1)抑制剂替雷利珠单抗治疗。治疗后,患者出现寒战、高热和面部潮红,随后休克。相关检查结果显示严重的多器官损伤,以及白细胞介素-6和降钙素原(PCT)水平显著升高。最初,患者被诊断为与替雷利珠单抗引起的细胞因子释放综合征相关的免疫相关不良事件(irAEs)或严重细菌感染。然而,当停止替雷利珠单抗治疗并重新应用CAPEOX化疗方案时,类似症状再次出现。经过筛查,最终确定奥沙利铂引起的严重过敏反应(HSR)是这些症状的根本原因。随后进行了文献综述,发现严重的奥沙利铂相关HSR很少见,因此本病例具有非典型性。本病例未表现出常见的HSR症状,如皮肤和呼吸道症状。然而,患者出现了严重的多器官损伤,在奥沙利铂化疗联合PD-1抑制剂治疗时被误诊为irAE。此外,这种明显的严重奥沙利铂相关HSR导致PCT水平显著升高,被误诊为严重细菌感染,从而阻止了糖皮质激素的使用。这反过来又加重了该患者的损伤。