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苯达莫司汀淋巴细胞清除是侵袭性 B 细胞淋巴瘤 axicabtagene ciloleucel 治疗中氟达拉滨联合环磷酰胺淋巴细胞清除的耐受性良好替代方案

英文原题:Bendamustine lymphodepletion is a well-tolerated alternative to fludarabine and cyclophosphamide lymphodepletion for axicabtagene ciloleucel therapy for aggressive B-cell lymphoma.

查看英文原题

Bendamustine lymphodepletion is a well-tolerated alternative to fludarabine and cyclophosphamide lymphodepletion for axicabtagene ciloleucel therapy for aggressive B-cell lymphoma.

PubMed 2023/09/05(内容时间) Am J Hematol Q1 · IF 9.4(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。

中文摘要

氟达拉滨/环磷酰胺(Flu/Cy)是淋巴瘤标准 CAR-T 细胞治疗前常用的淋巴细胞清除(LD)方案。目前仍需测试替代 LD 方案,以维持疗效、提高安全性,并应对近期全国性氟达拉滨短缺等问题。

本研究回顾性评估在本机构接受 axicabtagene ciloleucel(axi-cel)前,接受 bendamustine(n = 27)或 Flu/Cy(n = 42)LD 的复发/难治性侵袭性 B 细胞淋巴瘤患者结局。LD 前至 axi-cel 输注时,bendamustine 组和 Flu/Cy 组绝对淋巴细胞计数的中位变化分别为 −0.6 × 10⁹/L 和 −0.7 × 10⁹/L。bendamustine 组的最佳总体缓解率/完全缓解率为 77.8%(95% CI:57.7%–91.4%)/48.1%(95% CI:28.7%–68.1%),Flu/Cy 组分别为 81.0%(95% CI:65.9%–91.4%)/50.0%(95% CI:34.2%–65.8%)。bendamustine 组和 Flu/Cy 组 6 个月 PFS 分别为 43.8%(95% CI:24.7%–61.3%)和 55.6%(95% CI:39.0%–69.3%);6 个月 OS 分别为 81.5%(95% CI:61.1%–91.8%)和 90.4%(95% CI:76.4%–96.3%)。

调整基线既往治疗线数和难治性疾病后,与 Flu/Cy 组相比,bendamustine 组发生进展/复发/死亡的风险未增加(调整后 HR:1.4;95% CI:0.7–2.8;p = 0.32),死亡风险也未增加(调整后 HR:1.6;95% CI:0.5–5.6;p = 0.46)。bendamustine 组和 Flu/Cy 组各级/3 级 CRS 发生率分别为 89%/3.7% 和 86%/4.8%;各级/3 级 ICANS 发生率分别为 30%/19% 和 55%/31%。Flu/Cy 组 3 级中性粒细胞减少患者更多(100% vs. 68%),但 3 级感染并发症相近(分别为 24% 和 19%)。与 Flu/Cy 组相比,更多患者在门诊接受 bendamustine LD 和 axi-cel 治疗,且未增加毒性,住院中位时间更短。

总之,接受 bendamustine LD 后续用 axi-cel 的患者疗效相当,任何级别 ICANS 更少。

展开英文摘要原文

Fludarabine/cyclophosphamide (Flu/Cy) is established for lymphodepletion (LD) prior to standard-of-care CAR T-cell therapy for lymphoma. There is ongoing need to test alternative LD regimens to preserve efficacy, improve safety, and address challenges including the recent national fludarabine shortage.

We retrospectively evaluated outcomes among patients with relapsed/refractory aggressive B-cell lymphoma who received bendamustine (n = 27) or Flu/Cy (n = 42) LD before axicabtagene ciloleucel (axi-cel) at our institution. The median change in absolute lymphocyte count from pre-LD to time of axi-cel infusion was -0. 6 10 9 /L in bendamustine cohort and -0. 7 10 9 /L in Flu/Cy cohort. The best overall response/complete response rates were 77. 8% (95% CI: 57. 7%-91. 4%)/48. 1% (95% CI: 28. 7%-68. 1%) among bendamustine cohort and 81. 0% (95% CI: 65. 9%-91. 4%)/50. 0% (95% CI: 34. 2%-65. 8%) among Flu/Cy cohort. Six-month progression-free survival were 43. 8% (95% CI: 24. 7%-61. 3%) and 55. 6% (95% CI: 39. 0%-69. 3%) in bendamustine and Flu/Cy cohorts, while 6-month overall survival were 81. 5% (95% CI: 61. 1%-91. 8%) and 90. 4% (95% CI: 76. 4%-96. 3%), respectively.

Relative to Flu/Cy-treated patients, bendamustine-treated patients did not show an increase in hazards associated with experiencing progression/relapse/death (aHR:1. 4 [95% CI: 0. 7-2. 8]; p = . 32) or death (aHR:1. 6 [95% CI: 0. 5-5. 6]; p = . 46), after adjusting for baseline number of prior therapies and refractory disease. Any grade/grade 3 CRS were observed in 89%/3. 7% and 86%/4.

8% among bendamustine and Flu/Cy cohorts, while any grade ICANS/grade 3 ICANS were observed in 30%/19% and 55%/31% respectively. While more Flu/Cy-treated patients experienced grade 3 neutropenia compared with bendamustine-treated patients (100% vs. 68%), grade 3 infectious complications were comparable (24% vs. 19% respectively). More patients received bendamustine LD and axi-cel as outpatient than Flu/Cy cohort, without increased toxicities and with shorter median inpatient stays.

In conclusion, we observed comparable efficacy and lower any grade ICANS among patients receiving bendamustine relative to Flu/Cy LD, followed by axi-cel.

论文信息

作者
Ong SY、Pak S、Mei M、Wang Y、Popplewell L、Baird JH、Herrera AF、Shouse G
单位
Department of Hematology/ Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, California, USA.United States
文献类型
美国 NIH 资助研究
期刊
American journal of hematology2023 Nov
原文标识
PubMed 37668287 · DOI 10.1002/ajh.27069