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采用减低强度的干细胞移植治疗伴有良好细胞遗传学特征的急性髓性白血病获得成功。

Successful treatment of acute myelogenous leukemia with favorable cytogenetics by reduced-intensity stem cell transplantation.

机构信息

Stem Cell Transplantation Center, Hokkaido University Hospital, Sapporo 060-8648, Japan.

出版信息

Int J Hematol. 2010 Mar;91(2):310-21. doi: 10.1007/s12185-009-0487-y. Epub 2010 Jan 20.

DOI:10.1007/s12185-009-0487-y
PMID:20087795
Abstract

Acute myelogenous leukemia (AML) with favorable cytogenetics responds well to chemotherapy. If the leukemia relapses, allogenic hematopoietic stem transplantation (allo-HSCT) is considered as a treatment option. Since the efficacy of reduced-intensity stem cell transplantation (RIST) for AML with favorable cytogenetics has not been established, we retrospectively analyzed the outcomes of allo-HSCT in AML patients according to cytogenetic risks. The outcome of allo-HSCT for AML patients with favorable cytogenetics seemed to be superior to that for AML patients with intermediate cytogenetics. In AML patients with favorable cytogenetics, the 3-year overall survival (OS) and relapse-free survival (RFS) rates were 88 and 76%, respectively, in the RIST group. Both the 3-year OS and RFS rates were 81% in the conventional stem cell transplantation (CST) group. The outcome of RIST for AML patients with favorable cytogenetics was comparable to that for patients who received CST despite the more advanced age and greater organ dysfunction in RIST group than in CST group. None of the patients died within 90 days after RIST. Moreover, there was no relapse in patients with favorable cytogenetics who were in hematological remission prior to RIST. Thus, RIST for AML patients with favorable cytogenetics in remission is safe and effective.

摘要

伴有利细胞遗传学的急性髓系白血病(AML)对化疗反应良好。如果白血病复发,异体造血干细胞移植(allo-HSCT)被认为是一种治疗选择。由于低强度干细胞移植(RIST)对伴有利细胞遗传学的 AML 的疗效尚未确定,我们根据细胞遗传学风险回顾性分析了伴有利细胞遗传学的 AML 患者 allo-HSCT 的结果。伴有利细胞遗传学的 AML 患者的 allo-HSCT 结果似乎优于伴中等细胞遗传学的 AML 患者。在伴有利细胞遗传学的 AML 患者中,RIST 组的 3 年总生存率(OS)和无复发生存率(RFS)分别为 88%和 76%。CST 组的 3 年 OS 和 RFS 率分别为 81%。尽管 RIST 组比 CST 组年龄更大,器官功能障碍更严重,但伴有利细胞遗传学的 AML 患者接受 RIST 的结果与接受 CST 的患者相当。RIST 后 90 天内无患者死亡。此外,在 RIST 前处于血液学缓解的伴有利细胞遗传学患者中无复发。因此,缓解期伴有利细胞遗传学的 AML 患者进行 RIST 是安全有效的。

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本文引用的文献

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Influence of conditioning regimens and stem cell sources on donor-type chimerism early after stem cell transplantation.预处理方案和干细胞来源对干细胞移植后早期供者型嵌合体的影响。
Ann Hematol. 2008 Dec;87(12):1003-8. doi: 10.1007/s00277-008-0542-4. Epub 2008 Jul 18.
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Allogeneic hematopoietic stem-cell transplantation for myeloid sarcoma: a retrospective study from the SFGM-TC.异基因造血干细胞移植治疗髓系肉瘤:来自SFGM-TC的一项回顾性研究
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急性髓系白血病的异基因干细胞移植:一种风险适应性方法。
Blood Rev. 2008 Nov;22(6):293-302. doi: 10.1016/j.blre.2008.03.008. Epub 2008 May 1.
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Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia.细胞遗传学正常的急性髓系白血病中的突变与治疗结果
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Excellent outcome of allogeneic hematopoietic stem cell transplantation using a conditioning regimen with medium-dose VP-16, cyclophosphamide and total-body irradiation for adult patients with acute lymphoblastic leukemia.采用中剂量VP-16、环磷酰胺和全身照射预处理方案对成年急性淋巴细胞白血病患者进行异基因造血干细胞移植的良好疗效。
Biol Blood Marrow Transplant. 2008 May;14(5):568-75. doi: 10.1016/j.bbmt.2008.02.018.
6
Donor lymphocyte infusion in the treatment of first hematological relapse after allogeneic stem-cell transplantation in adults with acute myeloid leukemia: a retrospective risk factors analysis and comparison with other strategies by the EBMT Acute Leukemia Working Party.供体淋巴细胞输注治疗成人急性髓系白血病异基因干细胞移植后首次血液学复发:EBMT急性白血病工作组的回顾性危险因素分析及与其他策略的比较
J Clin Oncol. 2007 Nov 1;25(31):4938-45. doi: 10.1200/JCO.2007.11.6053. Epub 2007 Oct 1.
7
Impact of cytogenetics on outcome of matched unrelated donor hematopoietic stem cell transplantation for acute myeloid leukemia in first or second complete remission.细胞遗传学对首次或第二次完全缓解的急性髓系白血病患者单倍体相合无关供者造血干细胞移植结局的影响
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J Clin Oncol. 2006 Jan 20;24(3):444-53. doi: 10.1200/JCO.2005.03.1765. Epub 2005 Dec 12.
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Early allogeneic stem-cell transplantation for young adults with acute myeloblastic leukemia in first complete remission: an intent-to-treat long-term analysis of the BGMT experience.年轻成人急性髓细胞白血病首次完全缓解后早期异基因干细胞移植:基于BGMT经验的意向性治疗长期分析
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