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Allogeneic hematopoietic stem cell transplantation for patients with relapsed/refractory systemic anaplastic large cell lymphoma. A retrospective analysis of the Lymphoma Working Party of the European Society for Blood and Marrow Transplantation

机译:异种造血干细胞移植患者复发/难治性全身性血压大细胞淋巴瘤。 欧洲血液移植淋巴瘤工作组的回顾性分析

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Information regarding the curative role of allogeneic stem cell transplantation (allo-HCT) in systemic anaplastic large cell lymphoma (sALCL) is scarce. We analyzed the results of allo-HCT in patients with relapsed/refractory sALCL with special emphasis on the role of brentuximab vedotin (BV) as a bridge to allo-HCT. Forty-four patients (24 females, median age 38 years) with sALCL were included. Twenty-three patients (52%) received BV before allo-HCT; BV-treated patients were more heavily pretreated (>= 3 lines of therapy in 74% vs. 38%, p = 0.04). Twenty-three patients (52%) were in complete remission (CR) at allo-HCT. Three-year nonrelapse mortality and incidence of relapse (IR) after allo-HCT were 7% and 40%, respectively. With a median follow-up of 39 (12-69) months for survivors, 3-year progression-free survival (PFS) and overall survival were 53% and 74%, respectively. Univariate analysis showed that heavily pretreated patients and those not in CR had a higher IR and a lower PFS. The use of BV before transplant did not impact on any of the outcomes. Allo-HCT is a curative therapeutic strategy in a significant proportion of patients with relapsed/refractory sALCL; BV does not seem to modify transplant-related outcomes but might be able to render more patients candidates for this curative treatment.
机译:关于同种异体干细胞移植(Allo-HCT)在全生物症型芳香大细胞淋巴瘤(SALCL)中的疗法作用的信息是稀缺的。我们分析了复发/难治性Salc患者的Allo-Hct的结果,特别强调了Brentuximab Vedotin(BV)作为对allo-hct的桥梁的作用。包括四十四名患者(24名女性,38岁)与Salc。二十三名患者(52%)在Allo-HCT之前接受BV; BV治疗的患者更严重预处理(> = 3种疗法,74%vs.38%,P = 0.04)。 23名患者(52%)在Allo-HCT的完全缓解(Cr)中。 allo-hct后,三年的非卷曲死亡率和复发发生率分别为7%和40%。对于幸存者的39(12-69)个月的中位随访,3年的无进展生存(PFS)和总生存率分别为53%和74%。单变量分析表明,严重预处理的患者和不在Cr中的人具有更高的IR和较低的PFS。移植前使用BV没有影响任何结果。 Allo-HCT是一种疗法治疗策略,其患者复发/难治性Salc1; BV似乎似乎没有修改移植相关的结果,但可能能够为这种治疗治疗提供更多患者候选人。

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