Durvalumab-induced Pure White Cell Aplasia.

IF 3.2 4区 医学 Q3 IMMUNOLOGY Journal of Immunotherapy Pub Date : 2023-10-30 DOI:10.1097/CJI.0000000000000491
Ji Lin, Paola Rodriguez-Martinez, Thein Hlaing Oo, Shuyu E, Jeffrey Jorgensen, Cristhiam M Rojas-Hernandez
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引用次数: 1

Abstract

Immune checkpoint inhibitors (ICI) have gained approval as a treatment for a wide array of cancers. Their mechanism of action prevents the inactivation of cytotoxic T-cells, allowing for its cytotoxic response. However, the upregulation of the immune system by ICI also leads to many undesired adverse events known as immune-related adverse events (irAEs), ranging from dermatologic manifestations, such as rashes, to inflammation of mucous membranes, to hematologic toxicities. Here, we report a case of ICI-induced pure white cell aplasia, secondary to the agent durvalumab, which responded to treatment with filgrastim, prednisone, and cyclosporine. ICI-neutropenia accounts for 0.6% of all irAEs or 17% of hematologic irAEs. Given the rarity of hematologic irAEs, the available treatment guidelines are based on expert consensus. As ICI becomes more widely used, we can expect an increase in the prevalence of rare irAEs as well. This case report aims to present a rare side effect of ICI and demonstrate its response to immunosuppressive therapy while providing guidance for future clinicians and further elucidating the mechanism behind these irAEs.

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杜伐单抗诱导的纯白细胞发育不全。
免疫检查点抑制剂(ICI)作为一种治疗多种癌症的药物已获得批准。它们的作用机制防止细胞毒性T细胞失活,从而产生细胞毒性反应。然而,ICI对免疫系统的上调也会导致许多被称为免疫相关不良事件(irAE)的不良事件,从皮疹等皮肤病表现到粘膜炎症,再到血液学毒性。在此,我们报告了一例ICI诱导的纯白细胞再生障碍,继发于药物杜伐单抗,该药物对非格拉司汀、泼尼松和环孢菌素治疗有反应。ICI中性粒细胞减少症占所有irAE的0.6%或血液学irAE的17%。鉴于血液系统irAE的罕见性,现有的治疗指南基于专家共识。随着ICI的使用越来越广泛,我们可以预期罕见irAE的患病率也会增加。本病例报告旨在介绍ICI的一种罕见副作用,并证明其对免疫抑制治疗的反应,同时为未来的临床医生提供指导,并进一步阐明这些irAE背后的机制。
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来源期刊
Journal of Immunotherapy
Journal of Immunotherapy 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
79
审稿时长
6-12 weeks
期刊介绍: Journal of Immunotherapy features rapid publication of articles on immunomodulators, lymphokines, antibodies, cells, and cell products in cancer biology and therapy. Laboratory and preclinical studies, as well as investigative clinical reports, are presented. The journal emphasizes basic mechanisms and methods for the rapid transfer of technology from the laboratory to the clinic. JIT contains full-length articles, review articles, and short communications.
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