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检查点抑制剂在霍奇金淋巴瘤治疗中不断演变的作用。

The evolving role of checkpoint inhibitors in the treatment of Hodgkin lymphoma.

作者信息

Cashen Amanda F

机构信息

Washington University School of Medicine, Siteman Cancer Center, St. Louis, MO, United States.

出版信息

Front Oncol. 2024 Oct 22;14:1392653. doi: 10.3389/fonc.2024.1392653. eCollection 2024.

Abstract

Since their initial approval as single agent therapy for multiply relapsed/refractory Hodgkin lymphoma (HL), the PD-1 inhibitors nivolumab and pembrolizumab have been incorporated into second-line salvage regimens, and they are being investigated in upfront therapy of newly diagnosed patients. As second-line therapy in combination with brentuximab vedotin or multi-agent chemotherapy, nivolumab and pembrolizumab provide high complete remission rates and durable progression-free survival after consolidative autologous stem cell transplant. Incorporation of these agents into frontline chemotherapy regimens is feasible, and early results from a Phase III trial of nivolumab-AVD compare favorably with the existing standard for advanced stage HL, brentuximab vedotin plus AVD. As nivolumab and pembrolizumab move into earlier lines of HL therapy, open research questions include the efficacy of checkpoint inhibitor regimens in patients who relapse after frontline exposure to nivolumab or pembrolizumab; the selection of patients with relapsed HL who can achieve durable remissions without autologous stem cell transplant; and the efficacy of the PD-1 inhibitors in the frontline therapy of patients with early stage Hodgkin lymphoma.

摘要

自最初被批准作为复发性/难治性霍奇金淋巴瘤(HL)的单药治疗药物以来,程序性死亡蛋白1(PD-1)抑制剂纳武单抗和帕博利珠单抗已被纳入二线挽救方案,并且正在对新诊断患者的一线治疗进行研究。作为与本妥昔单抗或多药化疗联合的二线治疗,纳武单抗和帕博利珠单抗在巩固性自体干细胞移植后可提供较高的完全缓解率和持久的无进展生存期。将这些药物纳入一线化疗方案是可行的,纳武单抗联合阿霉素、长春花碱和达卡巴嗪(AVD)的III期试验的早期结果与晚期HL的现有标准本妥昔单抗联合AVD相比更具优势。随着纳武单抗和帕博利珠单抗进入HL治疗的更前线,尚未解决的研究问题包括在一线接受纳武单抗或帕博利珠单抗治疗后复发的患者中检查点抑制剂方案的疗效;无需自体干细胞移植即可实现持久缓解的复发HL患者的选择;以及PD-1抑制剂在早期霍奇金淋巴瘤患者一线治疗中的疗效。

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本文引用的文献

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Immune Checkpoint Blockade for the Treatment of Hodgkin Lymphoma.免疫检查点阻断疗法治疗霍奇金淋巴瘤
Immunotargets Ther. 2022 Feb 23;11:1-10. doi: 10.2147/ITT.S284988. eCollection 2022.

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