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BEGEV 挽救方案治疗复发/难治性经典霍奇金淋巴瘤:真实世界经验。

BEGEV salvage regimen in relapsed/refractory classical Hodgkin lymphoma: a real-life experience.

机构信息

IRCCS-Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.

Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Università di Bologna, Bologna, Italy.

出版信息

J Cancer Res Clin Oncol. 2023 Mar;149(3):1043-1047. doi: 10.1007/s00432-022-03955-w. Epub 2022 Mar 3.

Abstract

PURPOSE

One of the most critical issues in the management of Hodgkin lymphoma (HL) patients who resulted as primary relapsed or refractory is to obtain a minimal disease status before autologous stem cell transplantation (ASCT). Finding a salvage regimen able to induce this status without severe toxicity would represent a major achievement in this setting.

METHODS

A single-center retrospective study was conducted to assess effectiveness and safety of BEGEV (bendamustine, gemcitabine, and vinorelbine) regimen as first salvage setting prior to ASCT in HL patients.

RESULTS

Forty-three patients were treated in our institution between October 2017 and November 2020. Median age at BEGEV therapy was 35.0 years (range 17.2- 70.0), and the median time from frontline therapy to the first cycle of BEGEV was 79.5 days (range 4-2267). At the end of treatment, 31 patients achieved a complete response (CR), with an overall response rate of 76.7%. Forty-one patients harvested CD34+ cells and 35/43 (81.4%) patients underwent ASCT. With a median follow-up of 22 months, 4 CR patients had disease relapse, yielding an estimated disease-free survival of 73.9% at 34 months. The estimated 2-year progression-free survival was 66.7%. Response to first-line chemotherapy did not significantly influence prognosis.

CONCLUSIONS

BEGEV regimen was well tolerated, and reversible haematological toxic effects were the most common adverse events. Real-life data on BEGEV regimen as first salvage setting showed a relevant rate of objective responses and a limited myelotoxicity with no impairment of a subsequent mobilization of peripheral blood stem cells.

摘要

目的

在接受自体干细胞移植(ASCT)之前,获得最小疾病状态是管理原发性复发或难治性霍奇金淋巴瘤(HL)患者的最关键问题之一。找到一种能够在没有严重毒性的情况下诱导这种状态的挽救方案,将是该领域的重大成就。

方法

进行了一项单中心回顾性研究,以评估 BEGEV(苯达莫司汀、吉西他滨和长春瑞滨)方案作为 HL 患者 ASCT 前首次挽救治疗的有效性和安全性。

结果

2017 年 10 月至 2020 年 11 月期间,我院共收治 43 例患者。BEGEV 治疗时的中位年龄为 35.0 岁(范围 17.2-70.0),从一线治疗到 BEGEV 第一周期的中位时间为 79.5 天(范围 4-2267)。治疗结束时,31 例患者达到完全缓解(CR),总体缓解率为 76.7%。41 例患者采集了 CD34+细胞,35/43(81.4%)例患者接受了 ASCT。中位随访 22 个月时,4 例 CR 患者疾病复发,34 个月时无病生存率估计为 73.9%。估计 2 年无进展生存率为 66.7%。一线化疗的缓解情况并未显著影响预后。

结论

BEGEV 方案耐受性良好,最常见的不良反应是可逆性血液学毒性。BEGEV 方案作为首次挽救治疗方案的真实数据显示,客观缓解率高,骨髓毒性有限,不影响随后外周血造血干细胞的动员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0359/11798052/caade18c7526/432_2022_3955_Fig1_HTML.jpg

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