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Unmanipulated haploidentical versus HLA-matched sibling allogeneic hematopoietic stem cell transplantation in relapsed/refractory acute myeloid leukemia: a retrospective study on behalf of the ALWP of the EBMT

机译:Unmanipulated Haploidentical对HLA匹配的兄弟同种异体造血干细胞移植在复发/难治性急性髓性白血病中:代表EBMT ALWP的回顾性研究

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摘要

Refractory or relapsed acute myeloid leukemia (R/R-AML) has poor prognosis. Allogeneic hematopoietic stem-cell transplantation (HSCT) may provide cure in this scenario. We compared outcomes of HSCT from HLA-identical (HLA-id, n = 1654) sibling or haploidentical (Haplo, n = 389) donors in patients with R/R-AML, performed during the period 2007-2015. The Haplo group included patients receiving an unmanipulated graft (post-transplant cyclophosphamide, n = 278; in vivo T-cell depletion, n = 95; or both, n = 16). Median age at HSCT was 52 (range 18-74) years. Median follow-up was 16 and 22 months for HLA-id sibling and Haplo recipients, respectively (p = 0.11). Compared to MSD, Haplo HSCT were performed more recently (2013 vs 2011, p < 0.01), at longer interval from diagnosis (7 vs 5 months, p < 0.01), more frequently using bone marrow as stem cell source (47% vs 8%, p < 0.01) and with a reduced intensity conditioning regimen (50% vs 43%, p = 0.03). Engraftment was higher (93% vs 83%, p < 0.01) in HLA-id sibling. In multivariate analysis, Haplo HSCT was associated with lower GVHD/relapse-free survival, inferior LFS and OS and higher NRM, mainly due to a higher rate of infections (41% vs 25%, p < 0.01). For R/R-AML, HLA-id sibling donors remain the gold standard, when available, due to higher mortality in Haplo without significant gain in disease control.
机译:难治性或复发急性髓性白血病(R / R-AML)预后差。同种异体造血干细胞移植(HSCT)可以在这种情况下提供治疗方法。在2007 - 2015年期间,在r / r-AML的患者中比较了HLA相同(HLA-ID,N = 1654)兄弟或HAPLOIDENTING(HAPLO,N = 389)供体的HSCT的结果。 HAPLO组包括接受非向接枝的患者(移植后的环磷酰胺,n = 278;在体内T细胞耗尽中,n = 95;或两者,n = 16)。 HSCT的中位年龄为52(范围18-74)年。 HLA-ID兄弟姐妹和HAPLO接受者中位后续行动分别为16岁和22个月(P = 0.11)。与MSD相比,HAPLO HSCT更新(2013年2011年,P <0.01),从诊断(7 Vs 5个月,P <0.01),更频繁地使用骨髓作为干细胞源(47%VS 8) %,P <0.01)和强度调节方案的减少(50%Vs 43%,P = 0.03)。在HLA-ID兄弟中,植入较高(93%vs 83%,p <0.01)。在多变量分析中,HAPLO HSCT与较低的GVHD /复发存活,较差的LFS和OS和较高的NRM相关,主要是由于较高的感染率(41%Vs 25%,P <0.01)。对于R / R-AML,HLA-ID兄弟举办者仍然是由于HAPLO的较高死亡率,而无需疾病控制的显着增益。

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  • 来源
    《Bone marrow transplantation》 |2019年第9期|共12页
  • 作者单位

    Hop St Antoine Dept Hematol Serv Hematol &

    Therapie Cellulaire Paris France;

    Acute Leukemia Working Party EBMT Paris France;

    Hop St Antoine Dept Hematol Serv Hematol &

    Therapie Cellulaire Paris France;

    IRCCS Osped San Raffaele Hematol &

    BMT Unit Milan Italy;

    Ludwig Maximilians Univ Munchen Univ Hosp Munich Grosshadern Dept Internal Med 3 Munich Germany;

    Univ Munster Dept Med Hematol &

    Oncol Munster Germany;

    Univ Klinikum Dresden Med Klin &

    Poliklin 1 Dresden Germany;

    Univ Hosp Essen West German Canc Ctr Dept Bone Marrow Transplantat Essen Germany;

    Univ Freiburg Dept Med Hematol Oncol Freiburg Germany;

    Osped San Martino Genova Dept Haematol Genova 2 Genoa Italy;

    Hannover Med Sch Dept Haematol Hemostasis Oncol &

    Stem Cell Transp Hannover Germany;

    First State Pavlov Med Univ St Petersburg St Petersburg Russia;

    Azienda Osped Univ Udine Div Hematol Udine Italy;

    Hop St Antoine Dept Hematol Serv Hematol &

    Therapie Cellulaire Paris France;

    IRCCS Bambino Gesu Childrens Hosp Dept Pediat Hematol &

    Oncol Rome Italy;

    Acute Leukemia Working Party EBMT Paris France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

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