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Hematopoietic stem cell transplantation for children with high risk acutelymphoblastic leukemia in first complete remission: a report from theAIEOP registry.

机译:首次完全缓解的高危急性淋巴细胞性白血病儿童的造血干细胞移植:AIEOP注册中心的报告。

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摘要

Children with high-risk acute lymphoblastic leukemia in first complete remission can benefit from allogeneic hematopoietic stem cell transplantation. We analyzed the outcome of 211 children with high-risk acute lymphoblastic leukemia in first complete remission given allogeneic transplant from 1990 to 2008; outcome of patients who, despite having the indication to transplantation and a suitable donor, did not receive the allograft for different reasons in the same time period was not analyzed. Sixty-nine patients (33%) were transplanted between 1990 and 1999, 58 (27%) between 2000 and 2005, and 84 (40%) between 2005 and 2008. A matched family donor was employed in 138 patients (65%) and an unrelated donor in 73 (35%). The 10-year probability of overall and disease-free survival was 63.4% and 61%, respectively. The 10-year cumulative incidence of transplantation-related mortality and relapse was 15% and 24%, respectively. After 1999, no differences in terms of both disease-free survival and transplantation-related mortality were observed in patients transplanted from unrelated or matched family donor. In multivariate analysis, grade IV acute graft-versus-host disease was an independent factor associated with worse disease-free survival. By contrast, grade I acute graft-versus-host disease and age at diagnosis between 1 and 9 years were favorable prognostic variables. Our study, not intended to evaluate whether transplantation is superior to chemotherapy for children with acute lymphoblastic leukemia in first complete remission and high-risk features, shows that the allograft cured more than 60% of these patients; in the most recent period, the outcome of matched family and unrelated donor recipients is comparable.
机译:初次完全缓解的高危急性淋巴细胞白血病患儿可受益于同种异体造血干细胞移植。我们分析了1990年至2008年间接受异基因移植的首次完全缓解的211例高危急性淋巴细胞白血病儿童的结局。没有分析尽管有移植指征和合适的供体但由于不同原因而在同一时间段内没有接受同种异体移植的患者的结局。 1990年至1999年之间移植了69例患者(33%),2000年至2005年之间进行了58例(27%),2005年至2008年之间进行了84例(40%)。138位患者(65%)和73个(35%)的无亲属捐助者。总体生存期和无病生存期的10年概率分别为63.4%和61%。与移植相关的死亡率和复发率的10年累积发生率分别为15%和24%。从1999年以后,从无亲属或相配家庭供体移植的患者中,无病生存期和与移植相关的死亡率均无差异。在多变量分析中,IV级急性移植物抗宿主病是与无病生存期恶化相关的独立因素。相比之下,I级急性移植物抗宿主病和诊断年龄在1至9岁之间是有利的预后变量。我们的研究无意评估在完全完全缓解和高风险特征的急性淋巴细胞白血病患儿中移植是否优于化学疗法,该研究表明同种异体移植治愈了这些患者中的60%以上。在最近时期,匹配的家庭和无亲属的捐赠者的结果是可比的。

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