研究动态
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高剂量化疗和自体干细胞移植用于复发或难治性原发性纵隔B细胞淋巴瘤。

HIGH-DOSE CHEMOTHERAPY AND AUTOLOGOUS STEM-CELL TRANSPLANT FOR RELAPSED OR REFRACTORY PRIMARY MEDIASTINAL B-CELL LYMPHOMA.

发表日期:2023 Aug 20
作者: Hanan Alkhaldi, Alec Reinhardt, Melissa Barnett, Suprateek Kundu, Chitra Hosing, Jeremy Ramdial, Neeraj Saini, Samer Srour, Amin Alousi, Partow Kebriaei, Uday Popat, Muzaffar Qazilbash, Richard Champlin, Elizabeth J Shpall, Allison Gulbis, Terri Lynn Shigle, Bouthaina Dabaja, Chelsea Pinnix, Sairah Ahmed, Raphael Steiner, Borje S Andersson, Yago Nieto
来源: Cellular & Molecular Immunology

摘要:

原发性纵隔大B细胞淋巴瘤(PMBCL)是一种罕见的侵袭性非何杰金淋巴瘤。含利妥昔单抗的化疗免疫疗法±放疗是标准的一线治疗方法。复发或难治(R/R)疾病长期以来一直采用拯救化疗后接受自体干细胞移植(ASCT)的高剂量化疗作为合适患者的治疗方案。我们对我中心2000年1月至2022年8月期间接受HDC/ASCT治疗的所有R/R PMBCL患者进行了回顾性分析。60名患者接受了利妥昔单抗-BEAM(N=37)或利妥昔单抗-吉西他滨/巴曲霉素/甲氨蝶呤(R-GemBuMel)±沃诺斯他的治疗,同时进行了ASCT。46名患者接受了纵隔放疗,无论是作为一线治疗的预-consolidation还是ASCT后治疗。在中位随访时间为6年(范围为0.3-21)时,整个组的5年无进展生存率(PFS)和总生存率(OS)分别为58%和77%,R-BEAM患者分别为51%和65%,而R-vorinostat/GemBuMel患者分别为69%和82%。多变量分析显示,ASCT时PET阴性(风险比[HR]为0.28)和只有1个器官受累(HR为0.33)与PFS改善独立相关。此外,接受R-vorinostat/GemBuMel(HR为0.23)是独立的有利预测指标。总之,HDC/ASCT在R/R PMBCL中是有效的,并且接受R-vorinostat/GemBuMel的患者具有改善的预后。版权所有 © 2023 Elsevier Inc. 发表。
Primary mediastinal large B cell lymphoma (PMBCL) is an uncommon aggressive type of non-Hodgkin lymphoma. Rituximab-containing chemoimmunotherapy ± radiation therapy (RT) is standard first-line treatment. Relapsed or refractory (R/R) disease has long been treated with salvage chemotherapy followed by high-dose chemotherapy (HDC) with autologous stem cell transplantation (ASCT) in appropriate patients. We retrospectively analyzed all patients with R/R PMBCL treated with HDC/ASCT at our center between January 2000 and August 2022. Sixty patients received rituximab-BEAM (N=37) or rituximab-gemcitabine/busulfan/melphalan (R-GemBuMel) ± vorinostat (N=23), with ASCT. Forty-six patients received mediastinal RT, either as prior consolidation of frontline therapy or following ASCT. At median follow-up of 6 years (range, 0.3-21), the 5-year progression-free survival (PFS) and overall survival (OS) rates of the whole group are 58% and 77%, respectively, 51% and 65%, respectively, for R-BEAM patients, and 69% and 82%, respectively, for R-vorinostat/GemBuMel patients. Multivariable analyses showed that negative PET at ASCT [hazard ratio (HR), 0.28)] and involvement of only 1 organ (HR, 0.33) were independently associated with improved PFS. In addition, receiving R-vorinostat/GemBuMel (HR, 0.23) was an independent favorable predictor of OS. In conclusion, HDC/ASCT is effective in R/R PMBCL, with improved outcomes in patients receiving R-vorinostat/GemBuMel.Copyright © 2023. Published by Elsevier Inc.