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Autologous hematopoietic stem cell transplantation for relapsed/refractory systemic anaplastic large cell lymphoma. A retrospective analysis of the lymphoma working party (LWP) of the EBMT

机译:复发/难治性全身促进大细胞淋巴瘤的自体造血干细胞移植。 ebmt淋巴瘤工作党(LWP)的回顾性分析

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Systemic anaplastic large cell lymphoma (sALCL) is a rare histological entity expressing the CD30 antigen that comprises around 11% of peripheral T-cell lymphoma. We analysed the outcome of patients with relapsed/refractory sALCL treated with autologous stem cell transplantation (auto-HCT). We included 65 adult patients (42 males; median age, 44 years); 24 patients had an ALK-ve sALCL. Fifty-one patients had chemosensitive disease at the time of transplant. Ten patients (15%) were treated with brentuximab vedotin (BV) before auto-HCT (median number of doses: 5). The median follow-up for surviving patients was 35 months (3-71). Three-year cumulative incidence of nonrelapse mortality and of relapse were 1.7% and 34%, respectively. Three-year progression-free survival and overall survival were 64% and 73%, respectively. No prognostic factors for any of the outcomes analysed were found in univariate analysis. There were no significant differences in any of the outcomes between patients who had received BV and the remainder. This is the largest analysis presented so far analysing the role of auto-HCT in patients with relapsed/refractory sALCL, showing a promising PFS and OS in this high-risk population. The potential impact of the administration of BV as salvage strategy before the procedure needs to be further elucidated.
机译:全身包生大细胞淋巴瘤(SALCL)是表达CD30抗原的稀有组织学实体,其包含约11%的外周T细胞淋巴瘤。我们分析了用自体干细胞移植(Auto-Hct)处理的复发/难治性Salc1患者的结果。我们包括65名成年患者(42名男性;中位年龄,44岁); 24名患者有ALK-VE SALCL。发生在移植时有五十一名患者进行了化学致病性疾病。在Auto-HCT之前用布伦妥昔单抗vEdotin(BV)处理10名患者(15%)(中位数:5)。存活患者的中位后续随访35个月(3-71)。非卷中死亡率和复发的三年累积发病率分别为1.7%和34%。三年的无进展生存和整体存活分别为64%和73%。在单变量分析中发现了分析的任何结果的预后因素。收到BV和剩余部分的患者之间的任何结果都没有显着差异。这是迄今为止所提出的最大分析,分析了自动HCT在复发/难治Salc患者中的作用,显示出这种高风险群体中有前途的PFS和OS。在程序需要进一步阐明之前,将BV作为救助策略的潜在影响进一步阐明。

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