Palermo G, Maisel D, Barrett M, Smith H, Duchateau-Nguyen G, Nguyen T, Yeh R-F, Dufour A, Robak T, Dornan D, Weisser M
Roche Pharma Research and Early Development, Innovation Center, Basel, Switzerland.
Roche Pharma Research and Early Development, Innovation Center, Penzberg, Germany.
Blood Cancer J. 2015 Oct 2;5(10):e353. doi: 10.1038/bcj.2015.82.
Chronic lymphocytic leukemia (CLL) is a heterogeneous disease. Various disease-related and patient-related factors have been shown to influence the course of the disease. The aim of this study was to identify novel biomarkers of significant clinical relevance. Pretreatment CD19-separated lymphocytes (n=237; discovery set) and peripheral blood mononuclear cells (n=92; validation set) from the REACH trial, a randomized phase III trial in relapsed CLL comparing rituximab plus fludarabine plus cyclophosphamide with fludarabine plus cyclophosphamide alone, underwent gene expression profiling. By using Cox regression survival analysis on the discovery set, we identified inositol polyphosphate-5-phosphatase F (INPP5F) as a prognostic factor for progression-free survival (P<0.001; hazard ratio (HR), 1.63; 95% confidence interval (CI), 1.35-1.98) and overall survival (P<0.001; HR, 1.47; 95% CI, 1.18-1.84), regardless of adjusting for known prognostic factors. These findings were confirmed on the validation set, suggesting that INPP5F may serve as a novel, easy-to-assess future prognostic biomarker for fludarabine-based therapy in CLL.
慢性淋巴细胞白血病(CLL)是一种异质性疾病。多种疾病相关因素和患者相关因素已被证明会影响疾病进程。本研究的目的是识别具有显著临床相关性的新型生物标志物。来自REACH试验(一项复发CLL的随机III期试验,比较利妥昔单抗联合氟达拉滨加环磷酰胺与单独使用氟达拉滨加环磷酰胺)的预处理CD19分离淋巴细胞(n = 237;发现集)和外周血单个核细胞(n = 92;验证集)进行了基因表达谱分析。通过对发现集进行Cox回归生存分析,我们确定肌醇多磷酸-5-磷酸酶F(INPP5F)是无进展生存期(P<0.001;风险比(HR),1.63;95%置信区间(CI),1.35 - 1.98)和总生存期(P<0.001;HR,1.47;95%CI,1.18 - 1.84)的预后因素,无论是否对已知预后因素进行校正。这些发现在验证集上得到了证实,表明INPP5F可能作为一种新型的、易于评估的未来预后生物标志物,用于CLL中基于氟达拉滨的治疗。