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首页> 外文期刊>Bone marrow transplantation >Outcome after failure of allogeneic hematopoietic stem cell transplantation in children with acute leukemia: a study by the societe Francophone de greffe de moelle et de therapie cellulaire (SFGM-TC)
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Outcome after failure of allogeneic hematopoietic stem cell transplantation in children with acute leukemia: a study by the societe Francophone de greffe de moelle et de therapie cellulaire (SFGM-TC)

机译:急性白血病儿童异种造血干细胞移植失败后的结果:Societe Francophone de Greffee de Moelle et de Therapie Cellulaire的研究(SFGM-TC)

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摘要

Allogeneic hematopoietic stem cell transplantation (SCT) contributes to improved outcome in childhood acute leukemia (AL). However, therapeutic options are poorly defined in the case of post-transplantation relapse. We aimed to compare treatment strategies in 334 consecutive children with acute leukemia relapse or progression after SCT in a recent 10-year period. Data could be analyzed in 288 patients (157 ALL, 123 AML and 8 biphenotypic AL) with a median age of 8.16 years at transplantation. The median delay from first SCT to relapse or progression was 182 days. The treatment consisted of chemotherapy alone (n = 108), chemotherapy followed by second SCT (n = 70), supportive/palliative care (n = 67), combination of chemotherapy and donor lymphocyte infusion (DLI; n = 30), or isolated reinfusion of donor lymphocytes (DLI; n = 13). The median OS duration after relapse was 164 days and differed according to therapy: DLI after chemotherapy = 385 days, second allograft = 391 days, chemotherapy = 174 days, DLI alone = 140 days, palliative care = 43 days. A second SCT or a combination of chemotherapy and DLI yielded similar outcome (hazard ratio (HR) = 0.85, P = 0.53) unlike chemotherapy alone (HR = 1.43 P = 0.04), palliative care (HR = 4.24, P<0.0001) or isolated DLI (HR = 1,94, P<0.04). Despite limitations in this retrospective setting, strategies including immunointervention appear superior to other approaches, mostly in AML.
机译:同种异体造血干细胞移植(SCT)有助于儿童急性白血病(A1)的改善结果。然而,在移植后复发的情况下,治疗选择差异很差。我们旨在在最近10年期间比较334名急性白血病复发或急性白血病复发或进展的治疗策略。可以在288名患者(157例,123AML和8个Biphotypic Al)中分析数据,中位年龄在移植时期为8.16年。从第一个SCT复发或进展的中位延迟为182天。该处理由单独的化学疗法(n = 108),化疗,然后是第二SCT(n = 70),支持性/姑息护理(n = 67),化疗和供体淋巴细胞输注的组合(Dli; n = 30),或分离重新注入供体淋巴细胞(DLI; n = 13)。复发后的中位数OS持续时间为164天,根据治疗差异:DLI化疗= 385天,第二次同种异体移植= 391天,化疗= 174天,DLI单独= 140天,姑息治疗= 43天。第二SCT或化疗和DLI的组合产生了类似的结果(危害比(HR)= 0.85,P = 0.53)与单独的化疗不同(HR = 1.43 P = 0.04),姑息治疗(HR = 4.24,P <0.0001)或孤立的DLI(HR = 1,94,P <0.04)。尽管在此回顾性设置中有局限性,但在包括免疫展开的策略上,似乎优于其他方法,主要是在AML中。

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  • 来源
    《Bone marrow transplantation 》 |2017年第5期| 共5页
  • 作者单位

    Hop Archet Serv Hematol Ctr Hosp Univ Nice 151 Route St Antoine Ginestiere F-06202 Nice France;

    CHU Nice Dept Publ Hlth Nice France;

    St Louis Hosp Hematol Transplantat Unit Paris France;

    Hop La Timone Dept Pediat Hematol Marseille France;

    Hosp Civils Lyon Inst Hematol &

    Oncol Paediat Lyon France;

    CHU Nantes Dept Pediat Hematol Nantes France;

    Pediat Oncohematol Dept Hop Enfants Bordeaux France;

    CHU Nancy Brabois Onco Hematol Dept Vandoeuvre Les Nancy France;

    CHU Strasbourg Onco Hematol Dept Pediat Strasbourg France;

    CHU Montpellier Pediat Oncohematol Dept Montpellier France;

    Jeanne Flandre Hosp Dept Pediat Hematol Oncol CHRU Lille France;

    CHU Rouen Pediat Oncohematol Dept Rouen France;

    CHU Grenoble Pediat Oncohematol Dept Grenoble France;

    CHU Liege Dept Haematol Liege Belgium;

    Soc Francaise Greffe Moelle &

    Therapie Cellulaire Lyon France;

    CHRU Lille Dept Hematol Lille France;

    St Antoine Hosp Dept Hematol Paris France;

    Hop Robert Debre Dept Pediat Hematol Paris France;

    CHU Nice Pediat Hematol Oncol Dept Hop Archet Nice France;

    Univ Nice Sophia Antipolis Nice 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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