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供者造血干细胞移植治疗伴有 t(6;9)(p23;q34)的急性髓系白血病显著改善患者预后:一项配对分析。

Allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia with t(6;9)(p23;q34) dramatically improves the patient prognosis: a matched-pair analysis.

机构信息

Department of Cellular Transplantation Biology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

出版信息

Leukemia. 2012 Mar;26(3):461-4. doi: 10.1038/leu.2011.229. Epub 2011 Aug 26.

DOI:10.1038/leu.2011.229
PMID:21869835
Abstract

Acute myeloid leukemia (AML) with t(6;9)(p23;q34) is well known to have a poor prognosis treated with chemotherapy and autotransplantation. The presence of this karyotype is an indicator for allogeneic hematopoietic stem cell transplantation (HSCT); however, the impact of t(6;9)(p23;q34) on the HSCT outcome remains unclear. We conducted a matched-pair analysis of de novo AML patients with and without t(6;9)(p23;q34) using data obtained from the Japanese HSCT data registry. A total of 57 patients with t(6;9)(p23;q34) received transplants between 1996 and 2007, and 171 of 2056 normal karyotype patients matched for age, disease status at HSCT and graft source were selected. The overall survival, disease-free survival, cumulative incidence of relapse and the non-relapse mortality in t(6;9)(p23;q34) patients were comparable to those for normal karyotype patients. A univariate analysis showed that t(6;9)(p23;q34) had no significant impact on the overall survival. These findings suggest that allogeneic HSCT may overcome the unfavorable impact of t(6;9)(p23;q34) as an independent prognostic factor.

摘要

伴有 t(6;9)(p23;q34) 的急性髓系白血病(AML)经化疗和自体移植治疗预后较差。存在这种核型是进行异基因造血干细胞移植(HSCT)的指征;然而,t(6;9)(p23;q34) 对 HSCT 结果的影响仍不清楚。我们使用从日本 HSCT 数据登记处获得的数据,对伴有和不伴有 t(6;9)(p23;q34) 的初发 AML 患者进行了配对分析。共有 57 例 t(6;9)(p23;q34) 患者在 1996 年至 2007 年间接受了移植,选择了年龄、HSCT 时疾病状态和移植物来源相匹配的 2056 例正常核型患者中的 171 例。t(6;9)(p23;q34) 患者的总生存率、无病生存率、复发累积发生率和非复发死亡率与正常核型患者相当。单因素分析表明,t(6;9)(p23;q34) 对总生存率没有显著影响。这些发现表明,异基因 HSCT 可能克服 t(6;9)(p23;q34) 作为独立预后因素的不利影响。

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