首页> 外文期刊>Oncology letters >Analysis of ERCC1, BRCA1, RRM1 and TUBB3 as predictors of prognosis in patients with non-small cell lung cancer who received cisplatin-based adjuvant chemotherapy: A prospective study
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Analysis of ERCC1, BRCA1, RRM1 and TUBB3 as predictors of prognosis in patients with non-small cell lung cancer who received cisplatin-based adjuvant chemotherapy: A prospective study

机译:ERCC1,BRCA1,RRM1和TUBB3作为以顺铂为基础的辅助化疗的非小细胞肺癌患者预后的预测因素:一项前瞻性研究

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摘要

Although adjuvant platinum-based chemotherapy has been demonstrated to improve survival in patients with completely resected non-small cell lung cancer (NSCLC), individualized approaches to therapy are urgently required to improve the treatment efficacy and reduce unnecessary toxicity. It was hypothesized in the present study that the protein levels of excision repair cross-complementation group 1 (ERCC1), breast cancer 1 (BRCA1), ribonucleotide reductase M1 (RRM1) and class III beta-tubulin (TUBB3) may influence the therapeutic effect of adjuvant cisplatin-based chemotherapy. The expression of ERCC1, BRCA1, RRM1 and TUBB3 in tissues obtained from 84 patients with NSCLC was analyzed in the present non-interventional study by immunohistochemistry prior to adjuvant chemotherapy. All patients received adjuvant cisplatin-based chemotherapy. The primary endpoint in the present study was disease free survival (DFS). Out of the 84 tumors, the expression of ERCC1, BRCA1, RRM1 and TUBB3 was identified in 46 (55%), 11(13%), 73 (87%) and 76 (90%) tissues, respectively. A beneficial response to adjuvant cisplatin-based chemotherapy in DFS was associated with the absence of the expression of ERCC1 [hazard ratio (HR), 2.166; 95% confidence interval (CI), 1.049-4.474; P=0.037] and BRCA1 (HR, 2.419; 95% CI, 1.127-5.193; P=0.023), but not with the expression status of RRM1 (HR, 0.568; 95% CI, 0.234-1.379; P=0.212) or TUBB3 (HR, 1.874; 95% CI, 0.448-7.842; P=0.39). In addition, patients lacking the expression of ERCC1 and BRCA1 benefited more from adjuvant cisplatin-based chemotherapy compared with patients that expressed either ERCC1 or BRCA1 (HR, 3.102; 95% CI, 1.343-7:163; P=0.008). The expression of ERCC1 and BRCA1 was significantly associated with the DFS time in patients with NSCLC treated with adjuvant cisplatin-based chemotherapy, respectively. The combination of the ERCC1 and BRCA1 expression levels may be a promising prognostic prediction for adjuvant cisplatin-based chemotherapy.
机译:尽管已证明基于铂的辅助化疗可改善完全切除的非小细胞肺癌(NSCLC)患者的生存率,但迫切需要个性化的治疗方法以提高治疗效果并减少不必要的毒性。在本研究中假设切除修复交叉互补组1(ERCC1),乳腺癌1(BRCA1),核糖核苷酸还原酶M1(RRM1​​)和III类β-微管蛋白(TUBB3)的蛋白水平可能影响治疗效果基于顺铂的辅助化疗。在本项非介入研究中,在辅助化疗之前,通过免疫组织化学分析了84例NSCLC患者的组织中ERCC1,BRCA1,RRM1和TUBB3的表达。所有患者均接受基于顺铂的辅助化疗。本研究的主要终点是无病生存期(DFS)。在这84种肿瘤中,分别在46(55%),11(13%),73(87%)和76(90%)组织中鉴定了ERCC1,BRCA1,RRM1和TUBB3的表达。 DFS中对基于顺铂的辅助化疗的有益反应与ERCC1的表达缺失有关[危险比(HR),2.166; 95%置信区间(CI),1.049-4.474; P = 0.037]和BRCA1(HR,2.419; 95%CI,1.127-5.193; P = 0.023),但不具有RRM1的表达状态(HR,0.568; 95%CI,0.234-1.379; P = 0.212)或TUBB3(HR,1.874; 95%CI,0.448-7.842; P = 0.39)。此外,与表达ERCC1或BRCA1的患者相比,缺乏ERCC1和BRCA1表达的患者从顺铂辅助化疗中获益更多(HR,3.102; 95%CI,1.343-7:163; P = 0.008)。在以顺铂为基础的辅助化疗的NSCLC患者中,ERCC1和BRCA1的表达与DFS时间显着相关。 ERCC1和BRCA1表达水平的组合可能是基于顺铂的辅助化疗的有希望的预后预测。

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