免疫检查点抑制剂诱导的鳞状细胞癌患者的噬血细胞淋巴组织细胞增多症。

IF 1.3 Q4 HEMATOLOGY
Journal of hematology Pub Date : 2022-08-01 Epub Date: 2022-08-30 DOI:10.14740/jh1033
Rosalyn Marar, Sruti Prathivadhi-Bhayankaram, Mridula Krishnan
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引用次数: 4

摘要

程序性细胞死亡蛋白1 (PD-1)检查点抑制剂(如pembrolizumab)是用于治疗各种晚期恶性肿瘤的新疗法,并在多项研究中显示可提高患者生存率。然而,这些药物的毒性从轻微的副作用(如皮炎)到危及生命的并发症不等。我们报告了一个80岁的患者,假定皮肤原发鳞状细胞癌(SCC),经派姆单抗诱导的噬血细胞淋巴组织细胞增多症(HLH)。该患者最初表现为虚弱和全血细胞减少,被认为与免疫有关。她出现了进行性贫血,之后进一步的检查显示了对HLH的关注。她在类固醇、托珠单抗和依托泊苷治疗一个疗程后康复。据我们所知,该患者的病程是少数罕见的免疫检查点抑制剂(ICI)介导的HLH病例之一。该病例强调了早期诊断和识别HLH作为与ICI治疗相关的潜在毒性的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immune Checkpoint Inhibitor-Induced Hemophagocytic Lymphohistiocytosis in a Patient With Squamous Cell Carcinoma.

Immune Checkpoint Inhibitor-Induced Hemophagocytic Lymphohistiocytosis in a Patient With Squamous Cell Carcinoma.

Immune Checkpoint Inhibitor-Induced Hemophagocytic Lymphohistiocytosis in a Patient With Squamous Cell Carcinoma.

Programmed cell death protein 1 (PD-1) checkpoint inhibitors such as pembrolizumab are novel therapeutics used to treat various advanced malignancies and have been shown to increase patient survival in several studies. However, these drugs have a toxicity profile that ranges from mild side effects such as dermatitis to life-threatening complications. We present a case of pembrolizumab-induced hemophagocytic lymphohistiocytosis (HLH) in an 80-year-old patient with squamous cell carcinoma (SCC) of presumed cutaneous primary. This patient initially presented with weakness and pancytopenia, thought to be immune-related. She developed progressive anemia, after which further workup revealed concern for HLH. She recovered after a course of steroids, tocilizumab, and etoposide. To our knowledge, this patient's course is among a few rare cases of immune checkpoint inhibitor (ICI)-mediated HLH. This case highlights the need for early diagnosis and recognition of HLH as a potential toxicity related to ICI therapy.

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Journal of hematology
Journal of hematology HEMATOLOGY-
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