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新型细胞疗法时代B细胞淋巴瘤的异基因造血细胞移植:来自加拿大一家三级中心的经验

Allogeneic Hematopoietic Cell Transplant for B-Cell Lymphomas in the Era of Novel Cellular Therapies: Experience from a Tertiary Canadian Center.

作者信息

Castonguay Mathias, Roy Jean, Claveau Jean-Sébastien, Lachance Sylvie, Delisle Jean-Sébastien, Kiss Thomas, Cohen Sandra, Fleury Isabelle, Mollica Luigina, Ahmad Imran, Bambace Nadia, Bernard Léa, Roy Denis-Claude, Sauvageau Guy, Veilleux Olivier

机构信息

Hematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.

出版信息

Curr Oncol. 2025 May 20;32(5):285. doi: 10.3390/curroncol32050285.

Abstract

BACKGROUND

Allogeneic hematopoietic cell transplant (alloHCT) is a curative option for relapsed/refractory B-cell lymphomas (BCLs), but its role in the evolving field of cellular therapy is increasingly unclear as recent advances in transplant procedures have improved outcomes.

METHODS

This retrospective, single-center study included 55 BCL patients (large B-cell lymphoma-LBCL; indolent BCL; and mantle cell lymphoma-MCL) treated with alloHCT from 2015 to 2023 at Hôpital Maisonneuve-Rosemont. Primary endpoints were overall survival (OS) and progression-free survival (PFS); secondary endpoints included NRM and GVHD incidence.

RESULTS

A total of 55 patients were included (25 LBCLs, 16 indolent BCLs, 14 MCLs), and 76% of LBCLs were of indolent origin (Richter transformation, transformed follicular lymphoma). After a median follow-up of 6.1, 5.8 and 2.4 years for LBCLs, indolent BCLs and MCLs, their 5-year PFS and OS were 57.2% (IC 95%: 34.2-74.7) and 62.8% (IC 95%: 37.9-80.0), 81.2% (IC 95%: 52.5-93.5) and 93.8% (IC 95%: 63.2-99.1), and 39.0% (IC 95%: 14.3-63.3) and 68.1% (IC 95%: 35.4-86.8), respectively. The 5-year NRM was 16.9% (IC 95%: 8.2-28.3) with a relapse incidence of 23.4%. Overall/grade 3-4 acute GVHD occurred in 43.6% and 18.1% of patients. At 3 years, overall/moderate or severe chronic GVHD incidence was 49% and 34.5%.

CONCLUSIONS

AlloHCT remains a potentially curative option and should be considered for fit patients with chemosensitive FL or LBCLs of indolent origin and a low comorbidity index.

摘要

背景

异基因造血细胞移植(alloHCT)是复发/难治性B细胞淋巴瘤(BCL)的一种治愈性选择,但随着移植程序的最新进展改善了治疗结果,其在不断发展的细胞治疗领域中的作用越来越不明确。

方法

这项回顾性单中心研究纳入了2015年至2023年在蒙特利尔玫瑰圣母医院接受alloHCT治疗的55例BCL患者(大B细胞淋巴瘤-LBCL;惰性BCL;套细胞淋巴瘤-MCL)。主要终点是总生存期(OS)和无进展生存期(PFS);次要终点包括非复发死亡率(NRM)和移植物抗宿主病(GVHD)发生率。

结果

共纳入55例患者(25例LBCL、16例惰性BCL、14例MCL),76%的LBCL起源于惰性淋巴瘤(里氏转化、转化性滤泡淋巴瘤)。LBCL、惰性BCL和MCL的中位随访时间分别为6.1年、5.8年和2.4年,其5年PFS和OS分别为57.2%(95%置信区间:34.2-74.7)和62.8%(95%置信区间:37.9-80.0)、81.2%(95%置信区间:52.5-93.5)和93.8%(95%置信区间:63.2-99.1)、39.0%(95%置信区间:14.3-63.3)和68.1%(95%置信区间:35.4-86.8)。5年NRM为16.9%(95%置信区间:8.2-28.3),复发率为23.4%。43.6%的患者发生了总体/3-4级急性GVHD,18.1%的患者发生了此类情况。在3年时,总体/中度或重度慢性GVHD发生率分别为49%和34.5%。

结论

alloHCT仍然是一种潜在的治愈性选择,对于化疗敏感的惰性起源FL或LBCL且合并症指数低的合适患者应予以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cb6/12109923/54961271f7a5/curroncol-32-00285-g001.jpg

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