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抗 PD-1 阻断失败后复发难治性霍奇金淋巴瘤的化疗疗效。

Effectiveness of chemotherapy after anti-PD-1 blockade failure for relapsed and refractory Hodgkin lymphoma.

机构信息

Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy.

出版信息

Cancer Med. 2020 Nov;9(21):7830-7836. doi: 10.1002/cam4.3262. Epub 2020 Sep 2.

Abstract

Programmed death-1 (PD1) blockade is an efficient and safe therapeutic option in patients with relapsed/refractory (R/R) classical Hodgkin lymphoma (cHL). However, a substantial proportion of patients' progresses or loses the response to anti-PD1 treatment. We retrospectively investigated the effectiveness of salvage chemotherapies (CHT) for unsatisfactory response to anti-PD1, in 25 R/R cHL patients. Twenty-three patients (92%) were refractory to the last treatment before anti-PD1. After a median of 14 cycles (range 3-52), 68% (17/25) of patients had unsatisfactory responses to anti-PD1 therapy, whereas 6 had a partial response (PR) and 2 patients achieved complete response (CR), with an overall response rate (ORR) of 32%. After a median time of 1.5 months, 15 patients received a single agent treatment and 10 had a multi-agents regimen, due to the failure of PD1 blockade. The ORR was 60% (8 CR and 7 PR). Seven patients (3 in PR and 4 in CR) underwent a consolidation strategy with stem cell transplantation. Median progression-free survival (PFS) with salvage treatment was reached at 19.1 months, while median PFS after anti-PD1 has been reached at 8.2 months. After a median follow-up of 32.4 months, 6 patients died while 13 are still in CR. The median overall estimated from the start of CHT was not reached. The efficacy of treatment following anti-PD1 is not yet established, especially in lymphoma patients. To note, in our series, a subset of heavily pre-treated and chemo-refractory patients increased response rates to and survival with CHT given after exposure to immune-checkpoint inhibitors.

摘要

程序性死亡受体 1 (PD1) 阻断是复发/难治性 (R/R) 经典霍奇金淋巴瘤 (cHL) 患者的一种有效且安全的治疗选择。然而,相当一部分患者的病情进展或对 PD1 治疗失去反应。我们回顾性调查了 25 例 R/R cHL 患者对 PD1 治疗反应不佳时挽救性化疗 (CHT) 的有效性。23 例患者 (92%) 对 PD1 治疗前的最后一次治疗有耐药性。在中位 14 个周期 (范围 3-52) 后,68% (17/25) 的患者对 PD1 治疗的反应不满意,而 6 例患者获得部分缓解 (PR),2 例患者达到完全缓解 (CR),总缓解率 (ORR) 为 32%。中位时间为 1.5 个月后,由于 PD1 阻断失败,15 例患者接受单药治疗,10 例患者接受多药治疗。ORR 为 60% (8 例 CR 和 7 例 PR)。7 例患者 (3 例 PR 和 4 例 CR) 接受了干细胞移植的巩固治疗策略。挽救性治疗的中位无进展生存期 (PFS) 为 19.1 个月,而 PD1 治疗后的中位 PFS 为 8.2 个月。中位随访 32.4 个月后,6 例患者死亡,13 例仍处于 CR。从 CHT 开始时中位总体估计尚未达到。抗 PD1 治疗后的疗效尚未确定,尤其是在淋巴瘤患者中。需要注意的是,在我们的研究中,一组经过大量预处理和化疗耐药的患者,在接受免疫检查点抑制剂治疗后,增加了对 CHT 的反应率和生存时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9f/7643640/c1af83df46b0/CAM4-9-7830-g001.jpg

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