Lung cancer, predictive factor and ERCC1

Souad Souilah
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Abstract

Introduction: Excision repair cross-complementing group 1 (ERCC1) counteracts the cytotoxic effect of cisplatin through its role in DNA repair, and its expression level is a crucial factor for sensitivity to this drug. The objective of this study was to assess the impact of ERCC1 on tumor response and survival in patients with advanced non-small cell lung cancer (NSCLC) treated with a platinum-based regimen. Methods: Analysis of survival and tumor response based on the expression level of ERCC1 (detected by immunohistochemistry) in a cohort of NSCLC patients followed in a standard care setting. Results: Among the 77 cases of NSCLC included, ERCC1 expression was low in 64.9% of cases and high in 35.1% of cases. In the 52 patients treated with cisplatin, survival and tumor response were better in the low-expression group compared to the high-expression group: 14.35 months versus 9.49 months, p=0.022; Objective Response: 42.4% versus 0%, p=0.001. No significant difference was found based on protein expression level in patients treated with carboplatin. Conclusion: ERCC1 overexpression in patients treated with cisplatin predicts a poor tumor response and shorter survival.
肺癌、预测因子和 ERCC1
导言切除修复交叉互补基团1(ERCC1)通过其在DNA修复中的作用抵消顺铂的细胞毒性作用,其表达水平是顺铂药物敏感性的关键因素。本研究旨在评估ERCC1对接受铂类药物治疗的晚期非小细胞肺癌(NSCLC)患者的肿瘤反应和生存期的影响:方法:根据ERCC1的表达水平(通过免疫组化方法检测)分析标准治疗中NSCLC患者的生存率和肿瘤反应:在77例NSCLC患者中,64.9%的患者ERCC1表达水平较低,35.1%的患者ERCC1表达水平较高。在接受顺铂治疗的52例患者中,低表达组的生存期和肿瘤反应优于高表达组:14.35个月对9.49个月,P=0.022;客观反应:42.4%对0%:42.4%对0%,P=0.001。卡铂治疗患者的蛋白表达水平无明显差异:结论:顺铂治疗患者的ERCC1过表达预示着肿瘤反应较差和生存期较短。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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