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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Postremission Consolidation by Autologous Hematopoietic Cell Transplantation (HCT) for Acute Myeloid Leukemia in First Complete Remission (CR) and Negative Implications for Subsequent Allogeneic HCT in Second CR: A Study by the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation (EBMT)
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Postremission Consolidation by Autologous Hematopoietic Cell Transplantation (HCT) for Acute Myeloid Leukemia in First Complete Remission (CR) and Negative Implications for Subsequent Allogeneic HCT in Second CR: A Study by the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation (EBMT)

机译:自体造血细胞移植(HCT)对急性骨髓白血病(CR)中的急性髓白血病的影响,以及后续同种异体HCT在第二次CR中的负面影响:欧洲血液和骨髓移植社会急性白血病工作组的研究( ebmt)

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After autologous hematopoietic cell transplantation (HCT) in the first complete remission (CR1), patients with acute myeloid leukemia (AML) may relapse and undergo allogeneic HCT in the second complete remission (CR2). The aim of this study was to analyze the outcome of allogeneic HCT performed in CR2 comparing patients with prior consolidation by autologous HCT versus patients with chemotherapy consolidation. Included were 2619 adults with allogeneic HCT in CR2 from 2000 to 2017 with (n = 417) or without (n = 2202) prior autologous HCT. Patient groups were not entirely comparable; patients with prior autologous HCT were younger, had less often a favorable cytogenetic profile, had more commonly donors other than matched siblings, and more often received reduced-intensity conditioning. In multivariate analysis, nonrelapse mortality risks in patients with prior autologous HCT were 1.34 (1.07 to 1.67; P = .01) after adjustment for age, cytogenetic risk, transplant year, donor, conditioning intensity, sex matching, interval diagnosis-relapse, and relapse-allogeneic HCT as compared with chemotherapy consolidation. Similarly, risks of events in leukemia-free survival and graft-versus-host disease, relapse-free survival were higher with prior autologous HCT, 1.17 (1.01 to 1.35), P = .03 and 1.18 (1.03 to 1.35), P = .02, respectively. Risk of death was also higher, 1.13 (0.97 to 1.32), P = .1, but this was not significant. Postremission consolidation with autologous HCT for AML in CR1 increases toxicity of subsequent allogeneic HCT in CR2. (C) 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
机译:在第一次完全缓解(CR1)中的自体造血细胞移植(HCT)后,急性髓性白血病(AML)的患者可能在第二种完全缓解(CR2)中复发和经历同种异体HCT。本研究的目的是分析CR2在CR2中进行的同种异体HCT的结果比较,比较患者通过自体HCT与化疗固结患者进行了先前固结的患者。包括2619名成虫,在CR2中的同种异体HCT,从2000至2017年,(n = 417),或没有(n = 2202)以前的自体HCT。患者群体并不完全可比较;患有先前自体HCT的患者较年轻,较少往往是一种有利的细胞遗传学曲线,除了匹配的兄弟姐妹之外的更常见的供体,并且更常接受降低强度调节。在调整年龄,细胞遗传风险,移植年,供体,调节强度,性匹配,间隔诊断,间隔诊断,间隔诊断,间隔诊断 - 复发,以及患有年龄,细胞遗传风险,移植年,供体,调节性强度,性匹配,间隔诊断 - 复发,间隔诊断 - 复发和与化疗整合相比复发 - 异种HCT。类似地,无白血病生存和移植物与宿主疾病的事件风险,复发存活率与先前的自体HCT,1.17(1.01至1.35),P = .03和1.18(1.03至1.35),P =分别.02。死亡风险也更高,1.13(0.97至1.32),P = .1,但这并不重要。对CR1中AML的自体HCT的POStremissive固结增加了CR2中随后的同种异体HCT的毒性。 (c)2019年美国移植和细胞疗法。 elsevier公司发布

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