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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Allogeneic Hematopoietic Stem Cell Transplantation Following the Use of Hypomethylating Agents among Patients with Relapsed or Refractory AML: Findings from an International Retrospective Study
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Allogeneic Hematopoietic Stem Cell Transplantation Following the Use of Hypomethylating Agents among Patients with Relapsed or Refractory AML: Findings from an International Retrospective Study

机译:在经过复发或难治性AML的患者中使用低甲基化试剂后的同种异体造血干细胞移植:来自国际回顾性研究的结果

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摘要

Patients with primary refractory or relapsed acute myeloid leukemia (RR-AML) have very poor prognosis. Due to limited treatment options, some patients are treated with hypomethylating agents (HMAs) due to their tolerability. Little is known about the role of allogeneic hematopoietic stem cell transplantation (HSCT) following HMA therapy in this setting. We retrospectively analyzed an international cohort of 655 RR-AML patients who received HMA therapy to study patterns and outcomes with HSCT. Only 37 patients (5.6%) patients underwent HSCT after HMA therapy. The conditioning regimen was myeloablative in 57% and nonmyeloablative in 43%. Patients received matched unrelated donor, matched sibling, haploidentical and mismatched unrelated HSCT in 56%, 24%, 16% and 4% of cases, respectively. Acute GvHD and chronic GvHD were observed in 40% and 17% of patients. While the median OS for the entire cohort of patients was 15.3 months (95% CI 9.5 – 21.7 months), OS reached 29.7 months (95% CI 7.01 – not-reached) for patients who achieved a complete remission (CR) to HMA and no intervening therapies between HMA therapy and HSCT. Our study suggests that HMA therapy can effectively bridge some patients with RR-AML to HSCT.
机译:初级耐火或复发急性髓性白血病(RR-AML)的患者预后差。由于治疗方案有限,由于其耐受性,一些患者用低甲基化试剂(HMA)处理。关于在该环境中HMA治疗后的同种异体造血干细胞移植(HSCT)的作用很少。我们回顾性分析了655名RR-AML患者的国际队列,该患者接受HMA疗法以研究与HSCT的模式和结果。只有37名患者(5.6%)患者在HMA治疗后接受了HSCT。调节方案在57%和非粘合剂中以43%的非髓等级。患者接受匹配的无关捐助者,赛兄弟,寄生,寄和寄生和错配30%,24%,16%和4%的病例分别为56%。在40%和17%的患者中观察到急性GVHD和慢性GVHD。虽然整个患者队列的中位操作系统为15.3个月(95%CI 9.5-21.7个月),但对于达到HMA的完整缓解(CR)的患者,OS达到29.7个月(95%CI 7.01 - 未达到) HMA疗法和HSCT之间没有干预疗法。我们的研究表明,HMA疗法可以有效地将一些患者桥接到HSCT的RR-AML。

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