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Haploidentical transplantation outcomes for secondary acute myeloid leukemia: Acute Leukemia Working Party (ALWP) of the European Society for Blood and Marrow Transplantation (EBMT) study

机译:二级急性髓性白血病的寄生移植成果:欧洲血液和骨髓移植(EBMT)研究的急性白血病工作党(ALWP)

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摘要

Secondary acute myeloid leukemia (sAML) traditionally has inferior outcomes compared to de novo AML. Allogeneic hematopoietic cell transplantation (HCT) is the sole potentially curative therapy. This study analyzes the outcomes for unmanipulated haploidentical HCT (haploHCT) for sAML using the Acute Leukemia Working Party (ALWP) registry of the European Society for Blood and Marrow Transplantation (EBMT). We identified 154 patients with sAML who underwent haploHCT from 2006 to 2016. Median age at HCT was 60 years with time from diagnosis to HCT 5 months. At transplantation, 69 patients were in first CR and 85 had active disease. Fifty-seven (38.0%) patients underwent myeloablative conditioning and 97 (62.0%) reduced intensity conditioning (RIC) conditioning. Multivariate analysis showed that there was no difference in RI, nonrelapse mortality (NRM), leukemia free survival (LFS), overall survival (OS), or GVHD-free/relapse free survival (GRFS) for conditioning intensity, age, performance status, or graft source. Active disease was associated with higher RI and inferior LFS, OS, and GRFS compared with patients in CR at time of transplant. T-cell depletion with anti-thymoglobulin resulted in higher NRM and inferior LFS, OS, and GRFS compared to post-transplant cyclophosphamide (PTCy) (HR 2.25, 2.01, 2.16, and 1.73, respectively with P values .05). Our data shows that haploHCT is a feasible alternative for sAML when matched transplantation is unavailable.
机译:与De Novo AML相比,继发性急性髓白血病(SAML)传统上具有较差的结果。同种异体造血细胞移植(HCT)是唯一的潜在治疗疗法。本研究分析了使用欧洲血液和骨髓移植(EBMT)的急性白血病工作组(ALWP)登记处为SAML的Unmonulated Haploidentical HCT(HAPLOHCT)的结果。我们确定了154名患有2006年至2016年的HAPLOHCT的SAML患者.HCT的中位年龄从诊断到HCT 5个月的时间为60年。在移植过程中,69名患者首次CR,85例有活跃的疾病。五十七(38.0%)患者接受髓鞘调节和97(62.0%)的强度调节(RIC)调节。多变量分析表明,RI,非筛选死亡率(NRM),白血病自由生存(LFS),整体存活(OS),或GVHD /复发自由存活(GRF)对调理强度,年龄,性能状况,或移植源。与在移植时的CR患者相比,活性疾病与较高的RI和较差的LFS,OS和GRF相关。与抗胸腺酚蛋白的T细胞耗竭导致与移植后的环磷酰胺(PTCY)(HR 2.25,2.01,2.16和1.73分别具有P值的转移后环磷酰胺(PTCY)(HR 2.25,2.01,2.16和1.73)。我们的数据显示,当匹配的移植不可用时,HAPLOHCT是SAML的可行替代方案。

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  • 来源
    《American Journal of Hematology》 |2018年第6期|共9页
  • 作者单位

    Vanderbilt Univ Med Ctr Nashville TN 37235 USA;

    Univ Paris 06 INSERM UMR 938 St Antoine Hosp Dept Haematol EBMT Paris Study Off CEREST TC Paris;

    Osped San Raffaele Srl Milan Italy;

    Inst Paoli Calmettes Ctr Rech Cancerol Marseille Programme Transplantat &

    Therapie Cellulaire;

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

    Univ Klinikum Dresden Med Klin &

    Poliklin 1 Dresden Germany;

    Osped San Martino Genova Dept Haematol 2 Genoa Italy;

    Med Pk Hosp Stem Cell Transplant Unit Antalya Turkey;

    Osped Civile Dipartimento Ematol Med Trasfusionale &

    Biotecnol Pescara Italy;

    CHU Bordeaux Hop Haut leveque Pessac France;

    Ist Clin Humanitas Transplantat Unit Dept Haematol &

    Oncol Milan Italy;

    Univ Paris 06 INSERM UMR 938 St Antoine Hosp Dept Haematol EBMT Paris Study Off CEREST TC Paris;

    Univ Paris 06 INSERM UMR 938 St Antoine Hosp Dept Haematol EBMT Paris Study Off CEREST TC Paris;

    Univ Paris 06 INSERM UMR 938 St Antoine Hosp Dept Haematol EBMT Paris Study Off CEREST TC Paris;

    Univ Paris 06 Hop St Antoine Paris France;

    Vanderbilt Univ Med Ctr Nashville TN 37235 USA;

    Chaim Sheba Med Ctr Hematol Div Tel Hashomer Israel;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 血液及淋巴系疾病;
  • 关键词

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