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Clinical significance of up-regulated ID1 expression in Chinese de novo acute myeloid leukemia

机译:新发急性髓细胞性白血病中ID1表达上调的临床意义

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摘要

To investigate the clinical significance of ID1 expression in Chinese de novo AML patients. Real-time quantitative PCR was carried out to detect the status of ID1 expression in 102 de novo AML patients and 28 controls. ID1 transcript level was significantly increased in AML compared to normal controls (p=0.029). The age in the patients with high ID1 expression is significantly older than in those with low ID1 expression (p=0.044). ID1 overexpression occurred with the highest frequency in the patients with poor karyotype (7/7, 100%), lower frequency in the patients with intermediate karyotype (28/60, 47%), and the lowest frequency in the patients with favorable karyotype (12/31, 39%). Both whole AML and non-M3 patients with high ID1 expression had significantly lower rate of complete remission than those with low ID1 expression (p=0.007 and 0.038). ID1 high-expressed patients showed significantly shorter overall survival (OS) than ID1 low-expressed patients in both whole AML and non-M3 according to Kaplan-Meier analysis (p=0.007 and 0.040). However, multivariate analysis indicated that ID1 overexpression was not an independent risk factor in both whole AML and non-M3 patients. However, the adverse impact of ID1 overexpression on outcome was revealed by both Kaplan-Meier analysis and multivariate analysis in the non-M3 patients less than 60 years old. Our study reveals that ID1 overexpression may be associated with higher risk karyotype classification and act as an independent risk factor in young non-M3 patients.
机译:目的探讨中国新发AML患者中ID1表达的临床意义。进行实时定量PCR检测102例从头AML患者和28例对照中ID1表达的状态。与正常对照相比,AML中ID1转录水平显着增加(p = 0.029)。 ID1表达高的患者的年龄明显比ID1表达低的患者的年龄大(p = 0.044)。在弱核型患者中ID1过表达频率最高(7/7,100%),在中等核型患者中频率较低(28/60,47%),在有利核型患者中频率最低( 12 / 31,39%)。具有高ID1表达的整个AML患者和非M3患者的完全缓解率均比具有低ID1表达的患者低(p = 0.007和0.038)。根据Kaplan-Meier分析,在整个AML和非M3中,ID1高表达的患者的总生存期(OS)均明显短于ID1低表达的患者(p = 0.007和0.040)。但是,多变量分析表明,在整个AML和非M3患者中,ID1过表达都不是独立的危险因素。然而,Kaplan-Meier分析和多变量分析均在小于60岁的非M3患者中揭示了ID1过表达对预后的不利影响。我们的研究表明, ID1 过表达可能与较高风险的核型分类有关,并且是年轻的非M3患者的独立危险因素。

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