经 tagraxofusp 治疗后出现 CD123 表达缺失的浆细胞性树突状细胞肿瘤复发。

Rohit Gulati, Asma Abu-Salah, Tareq Salous, Mehdi Nassiri
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引用次数: 0

摘要

Tagraxofusp 是一种基于 CD123 的靶向免疫疗法,最近被批准用于治疗大疱性浆细胞性树突状细胞瘤(BPDCN),取得了很好的疗效。但也有一部分 BPDCN 对 tagraxofusp 产生了耐药性。这些耐药病例继续表达 CD123,这为 tagraxofusp 继续用于新型联合化疗以克服 BPDCN 的耐药性奠定了基础。在此,我们报告了一例患有 BPDCN 的老年男性患者,他在接受 tagraxofusp 的初始初治后获得了完全缓解。然而,治疗 1.5 年后,BPDCN 复发,CD123 表达消失。复发时,通过流式细胞术(在外周血和骨髓标本上进行)和骨髓凝块切片的免疫组化评估,对肿瘤进行了全面的免疫分型。复发时的肿瘤可诊断为缺乏 CD123 表达的 BPDCN。本病例凸显了目前和即将推出的基于 tagraxofusp 的多药疗法的潜在局限性,至少在一部分难治性 BPDCN 中是如此。我们相信,我们的报告将成为未来研究 BDPCN 替代耐药机制的前哨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relapse of tagraxofusp treated blastic plasmacytoid dendritic cell neoplasm with loss of CD123 expression.

Tagraxofusp, a CD123-based-targeted immunotherapy, was recently approved to treat blastic plasmacytoid dendritic cell neoplasm (BPDCN) with excellent response. Also, a subset of BPDCN shows resistance to tagraxofusp. These resistant cases continue to express CD123, which forms the basis of the continued utility of tagraxofusp in newer combination chemotherapies to overcome resistance in BPDCN. Herein, we report a case of an elderly male with BPDCN that achieved complete remission on initial primary treatment with tagraxofusp. However, BPDCN relapsed after 1.5 years while on treatment, with loss of CD123 expression. At relapse, the neoplasm was comprehensively immunophenotyped by flow cytometry (performed on both peripheral blood and bone marrow specimen) and by immunohistochemical evaluation of the bone marrow clot section. The neoplasm at relapse was diagnostic of BPDCN with a lack of CD123 expression. This case highlights a potential limitation of current and upcoming tagraxofusp-based multidrug therapies, at least in a subset of refractory BPDCN. We believe our report will serve as a sentinel to incite future investigations involving alternate resistance mechanisms in BDPCN.

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