...
首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Outcomes of pediatric bone marrow transplantation for leukemia and myelodysplasia using matched sibling, mismatched related, or matched unrelated donors.
【24h】

Outcomes of pediatric bone marrow transplantation for leukemia and myelodysplasia using matched sibling, mismatched related, or matched unrelated donors.

机译:使用匹配的同胞,不匹配的相关或匹配的不相关供体进行小儿骨髓移植治疗白血病和骨髓增生异常的结果。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Although some trials have allowed matched or single human leukocyte antigen (HLA)-mismatched related donors (mmRDs) along with HLA-matched sibling donors (MSDs) for pediatric bone marrow transplantation in early-stage hematologic malignancies, whether mmRD grafts lead to similar outcomes is not known. We compared patients < 18 years old reported to the Center for International Blood and Marrow Transplant Research with acute myeloid leukemia, acute lymphoblastic leukemia, chronic myeloid leukemia, and myelodysplastic syndrome undergoing allogeneic T-replete, myeloablative bone marrow transplantation between 1993 and 2006. In total, patients receiving bone marrow from 1208 MSDs, 266 8/8 allelic-matched unrelated donors (URDs), and 151 0-1 HLA-antigen mmRDs were studied. Multivariate analysis showed that recipients of MSD transplants had less transplantation-related mortality, acute graft-versus-host disease (GVHD), and chronic GVHD, along with better disease-free and overall survival than the URD and mmRD groups. No differences were observed in transplant-related mortality, acute and chronic GVHD, relapse, disease-free survival, or overall survival between the mmRD and URD groups. These data show that mmRD and 8/8 URD outcomes are similar, whereas MSD outcomes are superior to the other 2 sources. Whether allele level typing could identify mmRD recipients with better outcomes will not be known unless centers alter practice and type mmRD at the allele level.
机译:尽管一些试验已允许匹配的或单个的人类白细胞抗原(HLA)不匹配的相关供体(mmRD)以及HLA匹配的同胞供体(MSD)进行早期血液系统恶性肿瘤的小儿骨髓移植,但mmRD移植是否会导致相似的结果未知。我们将1993年至2006年间接受异体T淋巴细胞,清髓性骨髓移植的急性髓细胞性白血病,急性淋巴细胞性白血病,慢性髓性白血病和骨髓增生异常综合症报告给国际血液和骨髓移植研究中心报告的<18岁患者。总共研究了接受1208个MSD,266个8/8等位基因匹配的无关供体(URD)和151 0-1个HLA抗原mmRD接受骨髓的患者。多变量分析表明,与URD和mmRD组相比,MSD移植的接受者与移植相关的死亡率,急性移植物抗宿主病(GVHD)和慢性GVHD的患病率更低,无病生存率和总体生存率更高。在mmRD和URD组之间,在与移植相关的死亡率,急性和慢性GVHD,复发,无病生存或总体生存方面未见差异。这些数据表明mmRD和8/8 URD结果相似,而MSD结果优于其他两个来源。除非中心改变实践并在等位基因水平上键入mmRD,否则将不清楚等位基因水平分型是否可以识别出具有更好结果的mmRD受体。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号