Prajwal Dhakal, Mario Sy, G. Sutamtewagul, Eric Mou, Nanmeng Yu, N. Pemmaraju
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引用次数: 0
摘要
大疱性浆细胞树突状细胞瘤(BPDCN)是一种罕见的临床侵袭性血液系统恶性肿瘤,治疗方案有限。目前,标准的治疗策略包括临床试验;超剂量环磷酰胺、长春新碱、多柔比星和地塞米松(HCVAD)等化疗方案;以及 tagraxofusp-erzs(TAG,前身为 SL-401),它是首个针对 CD123 的同类靶向疗法。TAG于2018年12月获得美国食品和药物管理局批准用于一线BPDCN治疗,并逐渐成为化疗的替代疗法,提供了可能更有效、毒性更低的选择。然而,尽管结果令人鼓舞,但仍有患者可能对 TAG 单药治疗产生耐药性和/或有反应但最终复发。在此,我们将讨论一例使用 TAG 治疗的重要 BPDCN 患者,并回顾 BPDCN 的治疗策略。
Overcoming Tagraxofusp-Erzs Monotherapy Resistance in Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) in a Real-World Clinical Setting
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and clinically aggressive hematologic malignancy with limited treatment options. Currently, standard treatment strategies include clinical trials; chemotherapy regimens such as hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (HCVAD); and tagraxofusp-erzs (TAG, previously SL-401) which is the first-in-class targeted therapy against CD123. TAG received Food and Drug Administration approval for frontline BPDCN treatment in December 2018 and has increasingly become an alternative to chemotherapy, offering potentially more effective and less toxic options. However, despite promising results, there are still patients who may be resistant to TAG monotherapy and/or who respond but eventually relapse. Herein, we discuss an important patient case of BPDCN treated with TAG and review BPDCN treatment strategies.