← 返回

真实世界中加拿大难治或复发性弥漫大 B 细胞淋巴瘤患者的管理:RE-MIND2 研究亚组分析

英文原题:Management of Canadian patients with refractory or relapsed diffuse large B-cell lymphoma in the real world: a subanalysis of the RE-MIND2 study.

查看英文原题

Management of Canadian patients with refractory or relapsed diffuse large B-cell lymphoma in the real world: a subanalysis of the RE-MIND2 study.

PubMed 2025/11/11(内容时间) Oncologist Q2 · IF 4.7(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

我们的研究结果支持,不适合 ASCT 的患者接受常规挽救化疗后预后不良。

中文摘要

在加拿大当前复发/难治性弥漫大B细胞淋巴瘤(R/R DLBCL)治疗格局中,患者是否适合自体干细胞移植(ASCT)会影响挽救治疗选择。靶向CD19的CAR-T 细胞疗法改善了化疗难治性DLBCL患者结局,但仅适用于符合条件者。本研究是RE-MIND2观察性回顾队列研究的亚组分析,考察加拿大R/R DLBCL治疗模式。

回顾性收集2010至2020年在加拿大两家中心参加RE-MIND2患者的病历数据,采用描述性统计分析基线特征、启动的治疗及不同治疗线次的治疗持续时间。

共纳入109例患者;74.2%患者适合在二线(2L)接受ASCT,其中45.4%实际接受移植。适合三线(3L)和四线(4L)治疗ASCT的患者比例分别降至17.1%和5.9%。患者在3L和4L接受多种不同治疗。至2019年底,CAR-T 开始可用于3L和4L治疗。所有治疗线次的治疗中位持续时间均不足2.6个月;至下一次治疗的中位时间从4L的3.4个月到2L的5.3个月不等。

研究结果支持,不适合ASCT的患者接受传统挽救化疗后预后较差。在新型免疫疗法可用之前,对于不适合或未接受ASCT的加拿大R/R DLBCL患者,尤其是二线治疗后,并无明显统一标准治疗。

展开英文摘要原文

In the current Canadian treatment landscape for relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL), eligibility for autologous stem cell transplantation (ASCT) guides the choice of salvage treatment. CD19 chimeric antigen receptor T-cell (CAR-T) therapies have improved outcomes in patients with chemorefractory DLBCL, but access is limited to eligible patients. This subanalysis of the RE-MIND2 observational retrospective cohort study investigated treatment patterns for R/R DLBCL in Canada.

Data from patients enrolled in RE-MIND2 treated between 2010 and 2020 at 2 Canadian centers were retrospectively collected from health records. Descriptive statistics were used to analyze baseline characteristics, treatment initiated, and duration of treatment by line of therapy.

One hundred and nine patients were included; 74.2% of patients were eligible for ASCT as 2L therapy, and 45.4% received transplants. ASCT eligibility for third- (3L) and fourth-line (4L) therapy declined to 17.1% and 5.9%, respectively. Patients received a wide variety of treatments in 3 and 4L. CAR-T therapy became available in 3 and 4L by the end of 2019. Median durations of treatment were <2.6 months in all lines of therapy; median time to next treatment ranged from 3.4 months in 4L to 5.3 months in 2L.

Results of our study support that ASCT-ineligible patients have a poor prognosis with conventional salvage chemotherapy. Before the availability of novel immunotherapies, no apparent standard of care was observed for Canadian patients with R/R DLBCL who were ineligible for or did not receive ASCT, especially after 2L treatment.

论文信息

作者
Peters A、Nowakowski GS、Dabas R、Amoloja T、Xue Z、Koch C、Waltl EE、Fleury I
第一作者单位
Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.Canada
通讯作者单位
Hematology-Oncology and Cell Therapy University Institute, H&#xf4;pital Maisonneuve-Rosemont, Montreal University, Montreal, QC H1T 2M4, Canada.Canada
文献类型
观察性研究 · 多中心研究
期刊
The oncologist2025 Nov 11
原文标识
PubMed 41052305 · DOI 10.1093/oncolo/oyaf330