Bou Samra Elias, Klein Bernard, Commes Thérèse, Moreaux Jérôme
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.
Biomed Res Int. 2014;2014:423174. doi: 10.1155/2014/423174. Epub 2014 May 5.
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.
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。