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A multicenter trial of myeloablative clofarabine and busulfan conditioning for relapsed or primary induction failure AML not in remission at the time of allogeneic hematopoietic stem cell transplantation

机译:异基因造血干细胞移植治疗中复发或原发性诱导失败AML未缓解的清髓性氯法拉滨和环丁砜调理的多中心试验

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摘要

Allogeneic hematopoietic cell transplantation (HCT) may produce long-term survival in AML after relapse or primary induction failure (PIF). However, outcomes of HCT performed for AML not in remission are historically poor given high relapse rates and transplant-related mortality. Preliminary studies suggest conditioning with clofarabine and myeloablative busulfan (CloBu4) may exert significant anti-leukemic effects without excessive toxicity in refractory hematologic malignancies. A prospective multicenter phase II trial was conducted to determine the efficacy of CloBu4 for patients proceeding directly to HCT with AML not in remission. Seventy-one patients (median age: 56 years) received CloBu4. At day 30 after HCT, 90% achieved morphologic remission. The incidence of non-relapse mortality and relapse at 2 years was 25% and 55%, respectively. The 2-year overall survival (OS) and event-free survival (EFS) were 26% and 20%, respectively. Patients entering HCT in PIF had significantly greater EFS than those in relapse (34% vs 8%; P<0.01). Multivariate analysis comparing CloBu4 with a contemporaneous cohort (Center for International Blood and Marrow Transplantation Research) of AML not in remission receiving other myeloablative conditioning (n = 105) demonstrated similar OS (HR: 1.33, 95% confidence interval: 0.92–1.92; P = 0.12). HCT with myeloablative CloBu4 is associated with high early response rates and may produce durable remissions in select patients with AML not in remission.
机译:异基因造血细胞移植(HCT)可能在复发或原发性诱导衰竭(PIF)后在AML中产生长期存活。但是,鉴于复发率高和与移植相关的死亡率高,针对未缓解的AML进行HCT的结果历来较差。初步研究表明,使用氯法拉滨和清髓性白消安(CloBu4)进行调理可能在难治性血液系统恶性肿瘤中发挥重要的抗白血病作用,而不会产生过度毒性。进行了一项前瞻性多中心II期临床试验,以确定CloBu4对直接进入HCT且未缓解的AML患者的疗效。 71例患者(中位年龄:56岁)接受了CloBu4治疗。 HCT后第30天,有90%的患者达到了形态缓解。 2年时非复发死亡率和复发率分别为25%和55%。 2年总生存期(OS)和无事件生存期(EFS)分别为26%和20%。在PIF中进入HCT的患者的EFS明显高于复发患者(34%比8%; P <0.01)。多因素分析将CloBu4与同期同期(国际血液和骨髓移植研究中心)未接受其他清髓治疗的缓解患者(n = 105)进行比较,结果显示相似的OS(HR:1.33,95%置信区间:0.92-1.92; P = 0.12)。 HCT与清髓性CloBu4联合使用具有较高的早期缓解率,在某些未缓解的AML患者中可能产生持久缓解。

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