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异基因造血干细胞移植的疗效取决于急性髓系白血病首次疾病缓解时的细胞遗传学风险:一项荟萃分析。

Efficacy of allogeneic hematopoietic stem cell transplantation depends on cytogenetic risk for acute myeloid leukemia in first disease remission: a metaanalysis.

作者信息

Yanada Masamitsu, Matsuo Keitaro, Emi Nobuhiko, Naoe Tomoki

机构信息

Department of Hematology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Cancer. 2005 Apr 15;103(8):1652-8. doi: 10.1002/cncr.20945.

Abstract

BACKGROUND

The efficacy of allogeneic hematopoietic stem cell transplantation (allo-HSCT) from a human leukocyte antigen-identical sibling donor remains controversial for patients with acute myeloid leukemia (AML) in first complete disease remission (CR1). Because the karyotype identified at diagnosis is the most relevant prognostic factor for AML, it should be possible to assess the efficacy more accurately on the basis of cytogenetic risk.

METHODS

The authors performed a metaanalysis of five studies, which employed both natural randomization based on donor availability and intention-to-treat analysis, with overall survival as an outcome of interest. Metaregression analysis was then performed to identify the efficacy for patients stratified into the favorable, intermediate, and poor cytogenetic risk groups.

RESULTS

For the entire cohort, there was a statistically significant advantage with allo-HSCT in terms of overall survival with a summary hazard ratio of 1.15 (95% confidence interval, 1.01-1.32, P = 0.037) for the random-effect model. Metaregression analysis showed a significant coefficient of +0.24 for the poor cytogenetic risk group, and -0.25 for the favorable cytogenetic risk group, indicating that the benefit of allo-HSCT was further increased for the former, and lost for the latter. The coefficient for the intermediate cytogenetic risk group was +0.09, and was not statistically significant.

CONCLUSIONS

These findings suggested that the efficacy of allo-HSCT for patients with AML in CR1 depended on cytogenetic risk. The beneficial effect of allo-HSCT was yielded for the poor risk group, and probably for the intermediate risk groups, but was absent for the favorable risk group.

摘要

背景

对于首次完全缓解(CR1)的急性髓系白血病(AML)患者,来自人类白细胞抗原匹配同胞供体的异基因造血干细胞移植(allo-HSCT)的疗效仍存在争议。由于诊断时确定的核型是AML最相关的预后因素,因此应能够根据细胞遗传学风险更准确地评估疗效。

方法

作者对五项研究进行了荟萃分析,这些研究采用了基于供体可用性的自然随机化和意向性分析,将总生存作为感兴趣的结局。然后进行Meta回归分析,以确定分层为良好、中等和不良细胞遗传学风险组的患者的疗效。

结果

对于整个队列,随机效应模型显示allo-HSCT在总生存方面具有统计学显著优势,汇总风险比为1.15(95%置信区间,1.01-1.32,P = 0.037)。Meta回归分析显示,不良细胞遗传学风险组的系数为+0.24,良好细胞遗传学风险组的系数为-0.25,这表明allo-HSCT对前者的益处进一步增加,对后者则消失。中等细胞遗传学风险组的系数为+0.09,无统计学意义。

结论

这些发现表明,allo-HSCT对CR1期AML患者的疗效取决于细胞遗传学风险。allo-HSCT对不良风险组有益,可能对中等风险组也有益,但对良好风险组则无益处。

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