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基于基因表达的细胞遗传学正常急性髓系白血病患者风险评分的开发。

Development of gene expression-based risk score in cytogenetically normal acute myeloid leukemia patients.

作者信息

Bou Samra Elias, Klein Bernard, Commes Thérèse, Moreaux Jérôme

机构信息

Groupe d'études des transcriptomes, Université MONTPELLIER 2, Montpellier, F-34197 France .

出版信息

Oncotarget. 2012 Aug;3(8):824-32. doi: 10.18632/oncotarget.571.

Abstract

Patients with normal karyotype represent the single largest cytogenetic group of acute myeloid leukemia (AML), with highly heterogeneous clinical and molecular characteristics. In this study, we sought to determine new prognostic biomarkers in cytogenetically normal (CN)-AML patients. A gene expression (GE)-based risk score was built, summing up the prognostic value of 22 genes whose expression is associated with a bad prognosis in a training cohort of 163 patients. GE-based risk score allowed identifying a high-risk group of patients (53.4%) in two independent cohorts of CN-AML patients. GE-based risk score and EVI1 gene expression remained independent prognostic factors using multivariate Cox analyses. Combining GE-based risk score with EVI1 gene expression allowed the identification of three clinically different groups of patients in two independent cohorts of CN-AML patients. Thus, GE-based risk score is powerful to predict clinical outcome for CN-AML patients and may provide potential therapeutic advances.

摘要

核型正常的患者是急性髓系白血病(AML)中最大的细胞遗传学组,具有高度异质的临床和分子特征。在本研究中,我们试图确定细胞遗传学正常(CN)-AML患者的新预后生物标志物。构建了基于基因表达(GE)的风险评分,总结了163例患者训练队列中22个表达与不良预后相关的基因的预后价值。基于GE的风险评分能够在两个独立的CN-AML患者队列中识别出高危患者组(53.4%)。使用多变量Cox分析,基于GE的风险评分和EVI1基因表达仍然是独立的预后因素。将基于GE的风险评分与EVI1基因表达相结合,能够在两个独立的CN-AML患者队列中识别出三个临床不同的患者组。因此,基于GE的风险评分对于预测CN-AML患者的临床结局很有效,并且可能带来潜在的治疗进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c5f/3478459/096bde94d293/oncotarget-08-824-g001.jpg

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