Pembrolizumab治疗转移性肛门黑色素瘤诱导的细胞因子释放综合征。

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2025-07-01 eCollection Date: 2025-01-01 DOI:10.1155/crh/5444075
Erica Martel, Shijia Li, Mayssaa Hoteit, Zubin Bham
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引用次数: 0

摘要

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,通常在弥散期诊断,导致预后不良。这在嵌合抗原受体t细胞(CAR-T)治疗后得到了很好的描述,但在抗程序性死亡配体-1 (PDL-1)治疗后很少有报道。我们提出的病例86岁男性转移性肛门黑色素瘤谁发展CRS后,他的第四个周期的派姆单抗。他最初的表现被认为与败血症有关,因为他有高烧和低血压;然而,尽管进行了广泛的检查并广泛使用了抗生素,但仍缺乏改善,因此怀疑CRS是其症状的潜在病因。托珠单抗和类固醇治疗成功,症状得到缓解,无复发。该病例强调了免疫治疗诱导的CRS所带来的诊断和治疗挑战,并强调了早期识别以获得良好结果的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytokine Release Syndrome Induced by Pembrolizumab for Metastatic Anal Melanoma.

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.

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