噬血细胞性淋巴组织细胞增多症
医学
无容量
慢性淋巴细胞白血病
自身免疫性溶血性贫血
免疫系统
免疫学
不利影响
淋巴增殖性病變
贫血
免疫疗法
白血病
淋巴瘤
内科学
抗体
疾病
作者
Iris Dirven,An-Sofie Vander Mijnsbrugge,S. Mignon,Jens Tijtgat,Nicolas Kint,Bart Neyns
出处
期刊:Melanoma Research
[Ovid Technologies (Wolters Kluwer)]
日期:2023-04-28
卷期号:33 (4): 338-344
被引量:5
标识
DOI:10.1097/cmr.0000000000000895
摘要
Auto-immune hemolytic anemia (AIHA) and hemophagocytic lymphohistiocytosis (HLH) are both rare immune-related adverse events (irAEs) following treatment with immune checkpoint inhibitors. Consensus treatment guidelines are currently lacking. Patients with a solid malignancy and a concurrent lymphoproliferative disorder, such as chronic lymphocytic leukemia (CLL), might be more prone to develop hematological irAEs. We report the case history of two patients, diagnosed with CLL, who during treatment for metastatic melanoma with nivolumab, a PD-1 immune checkpoint blocking mAb, developed AIHA and HLH in combination with AIHA. Furthermore, we provide a review of the literature on published cases of immune-related AIHA and HLH and their correlation with CLL.
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