Zhang H, Li J, Zhang Y, Sun M, Zhao P, Zhang G, Jin C, Sun L, He M, Wang B, Zhang X
Department of Anesthesia, The Second Hospital of Jilin University, Changchun, China.
Department of Thoracic Surgery, The Second Hospital of Jilin University, Changchun, China.
Genet Mol Res. 2014 Dec 4;13(4):10215-22. doi: 10.4238/2014.December.4.16.
We conducted a prospective study to analyze the expression of the excision repair cross-complementing group 1 (ERCC1) and ribonucleotide reductase subunit M1 (RRM1) genes in 297 Chinese patients with advanced non-small cell lung cancer (NSCLC). The goal of this study was to evaluate these genes as potential biomarkers for prediction of tumor response and clinical outcome. Patients with unresectable, locally advanced or metastatic NSCLC were enrolled between September 2007 and September 2009, and they were followed up until September 2012. A fluorescence-based real-time detection method was used to quantify relative levels of ERCC1 and RRM1 cDNA. Relative amounts of ERCC1 and RRM1 cDNA were calculated by comparing to actin. By the end of follow-up, 132 patients had died and 165 patients experienced progression. The median overall survival time was 18.7 months (range, 1-60 months). The median levels of ERCC1 and RRM1 were 2.46 x 10(-2) and 0.97 x 10(-2), respectively. Patients with low ERCC1 expression had a significantly higher rate of complete response to chemotherapy, with an OR (95%CI) of 1.56 (1.03-2.47). Moreover, individuals with low levels of ERCC1 had longer overall survival than patients with high expression, with an adjusted hazard ratio (95%CI) of 0.57 (0.35-0.93). In summary, low ERCC1 mRNA expression was associated with better response to chemotherapy and correlated with longer survival in advanced NSCLC patients treated with platinum-based chemotherapy.
我们进行了一项前瞻性研究,以分析297例中国晚期非小细胞肺癌(NSCLC)患者中切除修复交叉互补基因1(ERCC1)和核糖核苷酸还原酶亚基M1(RRM1)基因的表达情况。本研究的目的是评估这些基因作为预测肿瘤反应和临床结局的潜在生物标志物。2007年9月至2009年9月纳入了不可切除、局部晚期或转移性NSCLC患者,并对其随访至2012年9月。采用基于荧光的实时检测方法定量ERCC1和RRM1 cDNA的相对水平。通过与肌动蛋白比较计算ERCC1和RRM1 cDNA的相对量。随访结束时,132例患者死亡,165例患者病情进展。中位总生存时间为18.7个月(范围1 - 60个月)。ERCC1和RRM1的中位水平分别为2.46×10⁻²和0.97×10⁻²。ERCC1低表达患者对化疗的完全缓解率显著更高,比值比(95%置信区间)为1.56(1.03 - 2.47)。此外,ERCC1水平低的个体总生存期比高表达患者更长,校正风险比(95%置信区间)为0.57(0.35 - 0.93)。总之,ERCC1 mRNA低表达与晚期NSCLC患者接受铂类化疗时对化疗的更好反应相关,并与更长生存期相关。