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异基因造血干细胞移植作为对大剂量阿糖胞苷为基础的诱导化疗耐药的急性髓系白血病患者的初始挽救治疗。

Allogeneic stem cell transplantation as initial salvage for patients with acute myeloid leukemia refractory to high-dose cytarabine-based induction chemotherapy.

机构信息

Department of Leukemia, U.T. M.D. Anderson Cancer Center, Houston, Texas.

出版信息

Am J Hematol. 2014 Apr;89(4):395-8. doi: 10.1002/ajh.23655. Epub 2014 Mar 7.

DOI:10.1002/ajh.23655
PMID:24375514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4140180/
Abstract

Outcomes of patients with acute myeloid leukemia (AML) who are refractory to high-dose Cytarabine (HiDAC)-based induction are dismal. Allogeneic hematopoietic stem cell transplantation (AHSCT) as initial salvage may be effective and potentially superior to conventional salvage chemotherapy. Eighteen percent (285 of 1597) of AML patients were primary refractory to HiDAC-based regimens at the MD Anderson Cancer Center between 1995 and 2009. AHSCT was the initial salvage in 28 cases. These patients were compared against 149 patients who received salvage chemotherapy, but never received AHSCT. Patients receiving salvage chemotherapy were older, had higher bone marrow blasts percentage, and higher incidence of unfavorable cytogenetics (P < 0.001). Median time from induction to AHSCT was 76 days. Objective response was achieved in 23 of 28 patients (82%) undergoing AHSCT. The incidence of grade III/IV acute and chronic graft versus-host-disease was 11% and 29%, respectively. Median follow up for living patients is 80 months. Median overall survival (OS) was 15.7 months and 2.9 months for AHSCT and chemotherapy, respectively (P < 0.001); the 3-year OS rates were 39% and 2%, respectively. ASHCT as initial salvage therapy was identified as an independent prognostic factor for survival in multivariate analysis (HR = 3.03; P < 0.001). Initial salvage therapy with AHSCT in patients with primary HiDAC refractory AML is feasible and may yield superior outcomes to salvage chemotherapy.

摘要

对于对高剂量阿糖胞苷(HiDAC)为基础的诱导有抗药性的急性髓细胞性白血病(AML)患者,其结果令人沮丧。同种异体造血干细胞移植(AHSCT)作为初始挽救治疗可能是有效的,并且可能优于常规挽救性化疗。1995 年至 2009 年间,MD 安德森癌症中心有 18%(1597 例中的 285 例)AML 患者对 HiDAC 为基础的方案原发性耐药。28 例患者接受了 AHSCT 作为初始挽救治疗。将这些患者与 149 例接受挽救性化疗但从未接受 AHSCT 的患者进行了比较。接受挽救性化疗的患者年龄较大,骨髓原始细胞比例较高,不良细胞遗传学的发生率较高(P < 0.001)。从诱导到 AHSCT 的中位时间为 76 天。接受 AHSCT 的 28 例患者中有 23 例(82%)获得了客观缓解。III/IV 级急性和慢性移植物抗宿主病的发生率分别为 11%和 29%。存活患者的中位随访时间为 80 个月。AHSCT 和化疗的中位总生存期(OS)分别为 15.7 个月和 2.9 个月(P < 0.001);3 年 OS 率分别为 39%和 2%。多因素分析显示,AHSCT 作为初始挽救治疗是生存的独立预后因素(HR = 3.03;P < 0.001)。对于原发性 HiDAC 耐药性 AML 患者,AHSCT 作为初始挽救治疗是可行的,并且可能优于挽救性化疗。

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Characteristics and outcome of patients with acute myeloid leukemia refractory to 1 cycle of high-dose cytarabine-based induction chemotherapy.对 1 周期高剂量阿糖胞苷为基础的诱导化疗难治的急性髓细胞白血病患者的特征和结局。
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