Identification of a 20-Gene Expression-Based Risk Score as a Predictor of Clinical Outcome in Chronic Lymphocytic Leukemia Patients

被引:15
|
作者
Samra, Elias Bou [1 ,2 ]
Klein, Bernard [1 ,2 ,3 ]
Commes, Therese [1 ,2 ,4 ]
Moreaux, Jerome [1 ,2 ,3 ]
机构
[1] INSERM, U1040, F-34197 Montpellier, France
[2] CHU Montpellier, Inst Res Biotherapy, F-34285 Montpellier, France
[3] Univ Montpellier I, UFR Med, F-34285 Montpellier, France
[4] Univ Montpellier 2, Inst Biol Computat, F-34095 Montpellier 5, France
关键词
ACUTE MYELOID-LEUKEMIA; WNT SIGNALING PATHWAY; LIPOPROTEIN-LIPASE; EXCISION-REPAIR; MUTATION STATUS; B-CELLS; DISEASE; SURVIVAL; ZAP-70; CONTRIBUTES;
D O I
10.1155/2014/423174
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
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页数:10
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