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以 Polatuzumab 为基础的方案或 CAR-T 细胞治疗复发/难治性弥漫大 B 细胞淋巴瘤患者——匹配队列分析

英文原题:Polatuzumab-based regimen or CAR T cell for patients with refractory/relapsed DLBCL-a matched cohort analysis.

查看英文原题

Polatuzumab-based regimen or CAR T cell for patients with refractory/relapsed DLBCL-a matched cohort analysis.

PubMed 2022/01/27(内容时间) Ann Hematol Q3 · IF 2.3(JCR 2025)

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中文摘要

基于Polatuzumab(Pola)的方案和CAR-T(CAR-T)细胞在复发/难治性弥漫性大B细胞淋巴瘤(R/R DLBCL)患者中相比传统化学免疫治疗提供了更优的结局。在这些策略之间进行选择仍存在争议。在一项回顾性“真实世界”研究中,比较了CAR-T 与Pola-利妥昔单抗(R)/Pola-苯达莫司汀(B)-R在2线治疗失败后的R/R DLBCL患者中的疗效。应用倾向性评分匹配,针对年龄、淋巴瘤类别(原发/转化)、既往治疗线数、东部肿瘤协作组体能状态和乳酸脱氢酶水平,以控制患者特征的差异。分析了缓解率、无进展生存期(PFS)和总生存期(OS)。

共纳入82例患者,接受CAR-T(n=41)或基于Pola的方案(n=41)治疗。CAR-T 未发生治疗相关死亡,而Pola为3例(7.3%)。CAR-T 的总体缓解率和完全缓解率分别为83%和58%,而基于Pola的方案为66%和44%(分别为p=0.077和p=0.18)。CAR-T 组和Pola组的中位随访时间分别为9个月(范围1-19.2)和16个月(范围0.7-25.3),CAR-T 的中位PFS尚未达到,而Pola为5.6个月(95% CI 3.6-7.6,p=0.014)。CAR-T 的中位OS尚未达到,而Pola为10.8个月(95% CI 2.2-19.4)(p=0.026)。

总之,在真实世界环境中,与基于Pola的方案相比,CAR-T 治疗在R/R DLBCL患者中实现了更优的PFS和OS。

展开英文摘要原文

Polatuzumab (Pola)-based regimens and chimeric antigen receptor T (CAR T) cells provide superior outcome compared to conventional chemoimmunotherapy in patients with relapsed/refractory diffuse large B cell lymphoma (R/R DLBCL). Choosing between these strategies remains controversial. The efficacy of CAR T versus Pola-rituximab(R) /Pola-bendamustine(B)-R in R/R DLBCL patients after failing 2 lines of treatment was compared in a retrospective, 'real-world' study. Propensity score matching, for age, lymphoma category (de-novo/transformed), number of prior lines, Eastern Cooperative Oncology Group performance status and lactate dehydrogenase level, was applied to control for differences in patients' characteristics. Response rate, progression-free survival (PFS) and overall survival (OS) were analyzed.

A total of 82 patients, treated with CAR T (n=41) or Pola-based regimens (n=41), were included. No treatment-related deaths occurred with CAR T vs. 3 (7. 3%) with Pola. The overall and complete response rates were 83% and 58% with CAR T vs. 66% and 44% with Pola-based-regimens (p=0. 077 and p=0. 18, respectively). At a median follow-up of 9 months (range 1-19. 2) and 16 months (range 0. 7-25.

3) for the CAR T and Pola arm respectively, the median PFS has not been reached for CAR T vs. 5. 6 months for Pola (95% CI 3. 6-7. 6, p=0. 014). Median OS has not been reached for CAR T vs. 10. 8 months (95% CI 2. 2-19. 4) for Pola (p=0. 026). To conclude, in a real-world setting, treatment with CAR T achieved superior PFS and OS compared to Pola-based regimens in patients with R/R DLBCL.

论文信息

作者
Avivi I、Perry C、Segman Y、Amit O、Bar-On Y、Katz OB、Gold R、Ribakovsky E
第一作者单位
Hematology Division, Sourasky Medical Center and the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.Israel
通讯作者单位
Hematology Division, Sourasky Medical Center and the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. ronram73@gmail.com.Israel
期刊
Annals of hematology2022 Apr
原文标识
PubMed 35083525 · DOI 10.1007/s00277-021-04749-9