...
首页> 外文期刊>Bone marrow transplantation >Autologous stem cell transplantation using modified TAM or combination of triple-alkylating agents conditioning regimens as one of the post-remission treatments in patients with adult acute myeloid leukemia in first complete remission.
【24h】

Autologous stem cell transplantation using modified TAM or combination of triple-alkylating agents conditioning regimens as one of the post-remission treatments in patients with adult acute myeloid leukemia in first complete remission.

机译:在首次完全缓解的成人急性髓细胞白血病患者中,使用改良的TAM或三烷基化试剂调理方案的组合进行自体干细胞移植是缓解后的治疗之一。

获取原文
获取原文并翻译 | 示例
           

摘要

A total of 174 newly diagnosed adult acute myeloid leukaemia (AML) patients were treated in first complete remission (CR1) using modified TAM or a combination of triple-alkylating agents followed by autologous transplantation (AT). Cytogenetic risk groups were classified and most patients received mobilized peripheral blood stem/progenitor cells (PBSCs). The infused cell dose consisted of a median of 4.1+/-2 (range, 1.2-17.1)x 10(6)/kg CD34+ cells. With a median follow-up of 51 months (range, 5-131 months) after CR1, the estimated 5-year disease-free survival (DFS) rate was 68 (95% confidence interval (CI), 63-73%) and the event-free survival rate at 5 years was 59 (95% CI, 54-64%). AML patients other than M3 subtype, the long-term DFS rate was 76, 33% for favourable and unfavourable risk groups, respectively. In all, 40 patients had relapses (40/174, 23%) at the median 15 months after CR1 (range, 8-66 months). Overall, seven patients (4%) died in connection with AT. The infused CD34+ cell dose (P=0.0389) was associated with survival by multivariate analysis. In conclusion, two novel conditioning regimens in AT are feasible for adults with variable risk AML followed for over a 10-year period.
机译:总共174例新诊断的成人急性髓细胞白血病(AML)患者在首次完全缓解(CR1)中接受治疗,方法是使用改良的TAM或三烷基化剂的组合,然后进行自体移植(AT)。对细胞遗传学风险组进行了分类,大多数患者接受了动员的外周血干/祖细胞(PBSC)。注入的细胞剂量由4.1 +/- 2(范围1.2-17.1)x 10(6)/ kg CD34 +细胞的中位数组成。 CR1后平均随访51个月(5-131个月),估计5年无病生存率(DFS)为68(95%置信区间(CI),63-73%), 5年无事件生存率是59(95%CI,54-64%)。除M3亚型以外的AML患者,长期和长期DFS发生率分别为有利和不利风险组,分别为33%和33%。共有40例患者在CR1后15个月的中位(8-66个月)复发(40 / 174,23%)。总体而言,有7名患者(占4%)死于AT。通过多变量分析,注入的CD34 +细胞剂量(P = 0.0389)与存活率相关。总之,对于患有可变风险AML的成年人,随访10年以上,在AT中采用两种新颖的调节方案是可行的。

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