Martel Erica, Li Shijia, Hoteit Mayssaa, Bham Zubin
Department of Internal Medicine at Bridgeport Hospital, Bridgeport, Connecticut, USA.
Section of Pulmonary, Critical Care at Bridgeport Hospital, Bridgeport, Connecticut, USA.
Case Rep Hematol. 2025 Jul 1;2025:5444075. doi: 10.1155/crh/5444075. eCollection 2025.
Cytokine release syndrome (CRS) is a rare systemic inflammatory response that can be triggered by certain drugs and infections, commonly diagnosed at a disseminated stage, leading to poor prognosis. This has been well described following chimeric antigen receptor T-cell (CAR-T) therapy but has rarely been reported following antiprogrammed death ligand-1 (PDL-1) therapy. We present the case of an 86-year-old male with metastatic anal melanoma who developed CRS after his 4th cycle of pembrolizumab. His initial presentation was thought to be related to sepsis given his high fevers and hypotension; however, given the lack of improvement despite an extensive workup and broad coverage with antibiotics, CRS was suspected as a potential etiology of his symptoms. Tocilizumab and steroids were successfully used and resulted in the resolution of symptoms without relapse. This case highlights the diagnostic and therapeutic challenges posed by immunotherapy-induced CRS and emphasizes the importance of early recognition to achieve good outcomes.
细胞因子释放综合征(CRS)是一种罕见的全身性炎症反应,可由某些药物和感染引发,通常在播散期被诊断出来,导致预后不良。嵌合抗原受体T细胞(CAR-T)治疗后对此已有充分描述,但抗程序性死亡配体1(PDL-1)治疗后鲜有报道。我们报告了一例86岁转移性肛门黑色素瘤男性患者,在接受第4周期帕博利珠单抗治疗后发生CRS。鉴于其高热和低血压,其最初表现被认为与脓毒症有关;然而,尽管进行了广泛检查并使用了广谱抗生素治疗,但病情仍无改善,因此怀疑CRS是其症状的潜在病因。托珠单抗和类固醇药物治疗成功,症状得以缓解且未复发。该病例凸显了免疫疗法诱导的CRS所带来的诊断和治疗挑战,并强调了早期识别以取得良好预后的重要性。