Laboratory of Tumor Cell Biology, School of Medicine, University of Crete, Heraklion, Crete, Greece.
Lung Cancer. 2013 Nov;82(2):324-9. doi: 10.1016/j.lungcan.2013.08.001. Epub 2013 Aug 11.
Excision-repair-cross-complement-1 (ERCC1) protein expression in tumor cells has been associated with resistance to platinum compounds, the backbone of treatment in NSCLC. In the current study the impact of the tumoral ERCC1 protein expression on the outcome of patients with advanced stage NSCLC treated with platinum-based chemotherapy, was investigated. Ninety-four patients with inoperable stage III-IV NSCLC, treated with platinum-based first-line chemotherapy, were retrospectively analyzed. Pretreatment tumor samples were analyzed for ERCC1 protein expression using immunohistochemistry. Response to treatment, time to tumor progression (TTP), and overall survival (OS) were correlated with patients' clinicopathological characteristics and ERCC1 protein expression on tumor cells. ERCC1 protein low expression was detected in 39 (41.5%) patients and did not correlate with patients' clinicopathological characteristics or response to chemotherapy. However, ERCC1 protein low expression showed a trend for better disease control rate (p = 0.059), longer TTP (5.3 vs. 3.2 months; p = 0.051) and significantly longer OS (18.7 vs. 9.7 months; p = 0.009). ERCC1 could have a role in refining prognosis and thus individualizing chemotherapy for advanced stage NSCLC.
肿瘤细胞中切除修复交叉互补基因 1(ERCC1)蛋白的表达与铂类化合物耐药有关,铂类化合物是 NSCLC 治疗的基础。本研究旨在探讨晚期 NSCLC 患者肿瘤 ERCC1 蛋白表达对铂类化疗疗效的影响。对 94 例不可切除的 III 期或 IV 期 NSCLC 患者进行回顾性分析,这些患者接受了铂类为基础的一线化疗。采用免疫组织化学法检测肿瘤标本中 ERCC1 蛋白的表达。根据患者的临床病理特征和肿瘤细胞中 ERCC1 蛋白的表达,将治疗反应、肿瘤进展时间(TTP)和总生存期(OS)与患者的临床病理特征和 ERCC1 蛋白表达进行相关性分析。39 例(41.5%)患者的 ERCC1 蛋白低表达,与患者的临床病理特征或化疗反应无相关性。然而,ERCC1 蛋白低表达的患者疾病控制率更高(p=0.059),TTP 更长(5.3 个月 vs. 3.2 个月;p=0.051),OS 显著延长(18.7 个月 vs. 9.7 个月;p=0.009)。ERCC1 可能在改善预后方面发挥作用,从而实现晚期 NSCLC 患者的个体化化疗。