首页> 美国卫生研究院文献>Indian Journal of Hematology Blood Transfusion >The Prognostic Relevance of BAALC and ERG Expression Levels in Cytogenetically Normal Pediatric Acute Myeloid Leukemia
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The Prognostic Relevance of BAALC and ERG Expression Levels in Cytogenetically Normal Pediatric Acute Myeloid Leukemia

机译:细胞遗传学正常的小儿急性髓细胞白血病中BAALC和ERG表达水平的预后相关性

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摘要

Cytogenetic aberrations are important prognostic factors in acute myeloid leukemia (AML). About 45 % of de novo adult AML and 20 % of pediatric AML lack cytogenetic abnormalities, so identification of predictive molecular markers might improve therapy. Mutation status of FLT3, NPM1 genes and gene expression levels of ERG, BAALC have been postulated as possible prognostic markers in pediatric AML with normal karyotype. Pretreatment blood samples from 47 cytogenetically normal AML patients were analysed for BAALC and ERG expression using real time RT-PCR. The patients were dichotomized at BAALC and ERG mean expression into low and high expression based on the median expression as cutoff. BAALC showed high expression in (24/47; 51.1 %) of patients and ERG high expression was detected in (22/47; 46.6 %). With follow-up for 1 year, patients with high BAALC and high ERG had inferior EFS (P = 0.001, P = 0.017 respectively), overall survival (P = 0.001, 0.08 respectively), and low rates of induction remission (P = 0.001, P = 0.0017 respectively) as compared to those with low expression. Also there was significant positive association between high expression of BAALC; ERG and FLT-ITD mutations (P = 0.016; P = 0.007 respectively). Multivariable analysis confirmed that high BAALC expression is an independent risk factor for EFS [HR for EFS 1.9(1.04–3.46) P = 0.037]; and OS [HR OS 1.55(1.7–3.36) P = 0.03]. In conclusion: Over expression of BAALC could predict adverse clinical outcome and may define important risk factor in cytogenetically normal pediatric AML.
机译:细胞遗传异常是急性髓细胞性白血病(AML)的重要预后因素。大约45%的新生AML和20%的小儿AML缺乏细胞遗传学异常,因此鉴定预测性分子标记可能会改善治疗。假定FRT3,NPM1基因的突变状态和ERG,BAALC的基因表达水平是正常核型的儿科AML的可能预后标记。使用实时RT-PCR分析了47位细胞遗传学正常的AML患者的预处理血样的BAALC和ERG表达。根据中位表达水平作为临界值,将患者在BAALC和ERG的平均表达水平下分为低表达和高表达。 BAALC在(24/47; 51.1%)患者中高表达,在(22/47; 46.6%)中检测到ERG高表达。随访1年,BAALC高和ERG高的患者的EFS较差(分别为P = 0.001,P = 0.017),总体生存率(分别为P = 0.001、0.08)和低诱导缓解率(P = 0.001) ,分别为P = 0.0017)。 BAALC的高表达之间也存在显着的正相关。 ERG和FLT-ITD突变(分别为 P = 0.016; P = 0.007)。多变量分析证实,BAALC的高表达是EFS的独立危险因素[HR的EFS 1.9(1.04-3.46) P = 0.037];和操作系统[HR OS 1.55(1.7–3.36) P = 0.03]。结论: BAALC 的过表达可以预测不良的临床结果,并可能是细胞遗传学正常的儿科AML的重要危险因素。

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