首页> 外文期刊>Bone marrow transplantation >Haplotype mismatched transplantation using high doses of peripheral blood CD34+ cells together with stratified conditioning regimens for high-risk adult acute myeloid leukemia patients: a pilot study in a single Korean institution.
【24h】

Haplotype mismatched transplantation using high doses of peripheral blood CD34+ cells together with stratified conditioning regimens for high-risk adult acute myeloid leukemia patients: a pilot study in a single Korean institution.

机译:高剂量成人急性髓性白血病患者使用大剂量外周血CD34 +细胞与分层条件治疗方案进行的单倍型错配移植:在单个韩国机构中进行的一项初步研究。

获取原文
获取原文并翻译 | 示例
           

摘要

A total of 11 high-risk Korean acute myeloid leukemia (AML) patients received stem cell transplantation from human leukocyte antigen (HLA) haploidentical donors. Specifically, for eight patients with 2-3 mismatched antigens and bidirectional vectors, we used a newly designed conditioning regimen that consists of total body irradiation, busulfex, ATG, and fludarabine. The median number of CD34+ cells infused was 15.4 x 10(6)/kg (range, 8-21.2). These patients received neither graft-versus-host disease (GvHD) prophylaxis nor post transplantation G-CSF. All of the patients who were followed up for a median of 6 months (range, 17 days-28 months) showed stable primary engraftment and had no acute GvHD or transplant-related mortality for 100 days post transplant. Three patients with high-risk or refractory disease eventually died in relapse, even with GvH-directed NK alloreactivity. However, the patients in complete remission (CR), with the exception of one patient who is alive at 18 months EFS, died at 4, 6, and 8 months post transplantation due to infections that were associated with delayed immune recovery. Our findings suggest that haploidentical transplantation represents a feasible treatment for patients with high-risk AML in CR, provided that a plan for the enhancement of immune recovery is implemented.
机译:共有11名高危韩国急性髓性白血病(AML)患者接受了来自人类白细胞抗原(HLA)单倍型供体的干细胞移植。具体而言,对于八名具有2-3个错配抗原和双向载体的患者,我们使用了一种新设计的调节方案,该方案包括全身照射,白消安,ATG和氟达拉滨。注入的CD34 +细胞的中位数为15.4 x 10(6)/ kg(范围8-21.2)。这些患者既未预防移植物抗宿主病(GvHD),也未接受移植后G-CSF。中位随访6个月(范围为17天至28个月)的所有患者均表现出稳定的初次植入,并且在移植后100天内无急性GvHD或与移植相关的死亡率。三名高危或难治性疾病患者最终死于复发,即使具有GvH定向的NK等位反应。但是,除了一位EFS存活18个月的患者之外,处于完全缓解(CR)的患者由于与免疫恢复延迟相关的感染而在移植后4、6和8个月死亡。我们的研究结果表明,如果实施了增强免疫恢复的计划,那么单倍体移植对于CR高危AML患者而言是一种可行的治疗方法。

著录项

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