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首页> 外文期刊>Cancer chemotherapy and pharmacology. >Predictive value of APE1, BRCA1, E1CC1 and TUBB3_ expression In patients with advanced non-small cell lung cancer (NSCLC) receiving first-line platinum-paditaxel chemotherapy
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Predictive value of APE1, BRCA1, E1CC1 and TUBB3_ expression In patients with advanced non-small cell lung cancer (NSCLC) receiving first-line platinum-paditaxel chemotherapy

机译:APE1,BRCA1,E1CC1和TUBB3_表达的预测价值在接受一线铂-帕他赛尔化疗的晚期非小细胞肺癌(NSCLC)患者中

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Purpose Drag resistance is not only one of the major obstacles to treatment but also a poor prognosis in advanced non-small cell lung cancer (NSCLC) patients. The aim of this study was to evaluate the predictive value of APE1, BRCA1, ERCC1 and TUBB3 in advanced NSCLC patients who received platinum-paclitaxel treatment. Methods One hundred and thirty-six advanced NSCLC patients, who were treated with first-line platinum-pacli-taxel chemotherapy, were enrolled in this study. The protein expression levels of APE1, BRCA1, ERCC1 and TUBB3 were assessed by immunohistochemistry and analyzed for the association with response to chemotherapy and progression-free survival (PFS) and overall survival (OS). Results Patients with negative expression of APE1, ERCC1 or TUBB3 benefited from platinum plus paclitaxel regimen chemotherapy. ERCC1-negative patients had better PFS (P = 0.016) and OS (P = 0.030) compared with positive patients. Similarly, the APEl-negative patients showed better PFS (P = 0.004) and longer OS though statistically insignificant. Multivariate analysis showed that APE1 and ERCC1 were independent predictor for PFS (HR 2.07; P = 0.004 and HR 1.66; P = 0.016) and OS (HR 1.99; P = 0.008 and HR 1.64; P = 0.040). Moreover, patients with both APE1- and ERCC1-negative or both APE1- and TUBB3-negative tumors had significantly higher response rate, longer median PFS and OS following treatment with platinum and paclitaxel (P < 0.05).Conclusion The data indicate that APE1, ERCC1 and TUBB3 could be a useful biomarker to predict clinical outcome in patients with advanced NSCLC receiving first-line platinum-paclitaxel chemotherapy.
机译:目的抗药性不仅是晚期非小细胞肺癌(NSCLC)患者治疗的主要障碍之一,而且预后差。这项研究的目的是评估APE1,BRCA1,ERCC1和TUBB3在接受​​铂-紫杉醇治疗的晚期NSCLC患者中的预测价值。方法纳入一线铂类-紫杉醇-紫杉醇一线化疗方案治疗的136例晚期NSCLC患者。通过免疫组织化学评估APE1,BRCA1,ERCC1和TUBB3的蛋白表达水平,并分析其与化学疗法和无进展生存期(PFS)和总生存期(OS)的相关性。结果APE1,ERCC1或TUBB3阴性表达的患者受益于铂加紫杉醇方案化疗。与阳性患者相比,ERCC1阴性患者的PFS(P = 0.016)和OS(P = 0.030)更好。同样,尽管在统计学上不显着,但APEl阴性患者表现出更好的PFS(P = 0.004)和更长的OS。多变量分析显示APE1和ERCC1是PFS(HR 2.07; P = 0.004和HR 1.66; P = 0.016)和OS(HR 1.99; P = 0.008和HR 1.64; P = 0.040)的独立预测因子。此外,APE1和ERCC1阴性或APE1和TUBB3阴性的患者在接受铂和紫杉醇治疗后有明显更高的缓解率,中位PFS和OS(P <0.05)。结论数据表明APE1, ERCC1和TUBB3可能是预测接受一线铂-紫杉醇化疗的晚期NSCLC患者临床结局的有用生物标志物。

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