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鉴定基于20个基因表达的风险评分作为慢性淋巴细胞白血病患者临床结局的预测指标。

Identification of a 20-gene expression-based risk score as a predictor of clinical outcome in chronic lymphocytic leukemia patients.

作者信息

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

机构信息

INSERM, U1040, F-34197, Institute of Research in Biotherapy, CHU Montpellier, 80 Avenue Augustin Fliche, 34285 Montpellier Cedex, France.

INSERM, U1040, F-34197, Institute of Research in Biotherapy, CHU Montpellier, 80 Avenue Augustin Fliche, 34285 Montpellier Cedex, France ; CHU Montpellier, Institute of Research in Biotherapy, Montpellier, 80 Avenue Augustin Fliche, 34285 Montpellier, France ; Université Montpellier 1, UFR Médecine, Montpellier, 80 Avenue Augustin Fliche, 34285 Montpellier, France.

出版信息

Biomed Res Int. 2014;2014:423174. doi: 10.1155/2014/423174. Epub 2014 May 5.

Abstract

Despite the improvement in treatment options, chronic lymphocytic leukemia (CLL) remains an incurable disease and patients show a heterogeneous clinical course requiring therapy for many of them. In the current work, we have built a 20-gene expression (GE)-based risk score predictive for patients overall survival and improving risk classification using microarray gene expression data. GE-based risk score allowed identifying a high-risk group associated with a significant shorter overall survival (OS) and time to treatment (TTT) (P ≤ .01), comprising 19.6% and 13.6% of the patients in two independent cohorts. GE-based risk score, and NRIP1 and TCF7 gene expression remained independent prognostic factors using multivariate Cox analyses and combination of GE-based risk score together with NRIP1 and TCF7 gene expression enabled the identification of three clinically distinct groups of CLL patients. Therefore, this GE-based risk score represents a powerful tool for risk stratification and outcome prediction of CLL patients and could thus be used to guide clinical and therapeutic decisions prospectively.

摘要

尽管治疗方案有所改进,但慢性淋巴细胞白血病(CLL)仍然是一种无法治愈的疾病,许多患者的临床病程各异,需要进行治疗。在当前的研究中,我们利用微阵列基因表达数据构建了一个基于20个基因表达(GE)的风险评分,用于预测患者的总生存期并改善风险分类。基于GE的风险评分能够识别出一个与显著缩短的总生存期(OS)和治疗时间(TTT)相关的高危组(P≤0.01),在两个独立队列中分别占患者的19.6%和13.6%。使用多变量Cox分析,基于GE的风险评分以及NRIP1和TCF7基因表达仍然是独立的预后因素,基于GE的风险评分与NRIP1和TCF7基因表达相结合能够识别出三组临床上不同的CLL患者。因此,这种基于GE的风险评分是CLL患者风险分层和预后预测的有力工具,从而可用于前瞻性地指导临床和治疗决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cea/4026849/102d15508677/BMRI2014-423174.001.jpg

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