Bronte Giuseppe, Silvestris Nicola, Castiglia Marta, Galvano Antonio, Passiglia Francesco, Sortino Giovanni, Cicero Giuseppe, Rolfo Christian, Peeters Marc, Bazan Viviana, Fanale Daniele, Giordano Antonio, Russo Antonio
Department of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
Medical Oncology Unit,National Cancer Institute "Giovanni Paolo II", Bari, Italy.
Oncotarget. 2015 Sep 22;6(28):24780-96. doi: 10.18632/oncotarget.4959.
Anti-epidermal growth factor receptor therapy with the monoclonal antibodies cetuximab and panitumumab is the main targeted treatment to combine with standard chemotherapy for metastatic colorectal cancer. Many clinical studies have shown the benefit of the addition of these agents for patients without mutations in the EGFR pathway. Many biomarkers, including KRAS and NRAS mutations, BRAF mutations, PIK3CA mutations, PTEN loss, AREG and EREG expression, and HER-2 amplification have already been identified to select responders to anti-EGFR agents. Among these alterations KRAS and NRAS mutations are currently recognized as the best predictive factors for primary resistance. Liquid biopsy, which helps to isolate circulating tumor DNA, is an innovative method to study both primary and acquired resistance to anti-EGFR monoclonal antibodies. However, high-sensitivity techniques should be used to enable the identification of a wide set of gene mutations related to resistance.
使用西妥昔单抗和帕尼单抗等单克隆抗体进行的抗表皮生长因子受体治疗,是转移性结直肠癌与标准化疗联合使用的主要靶向治疗方法。许多临床研究表明,对于表皮生长因子受体(EGFR)通路无突变的患者,添加这些药物有益。包括KRAS和NRAS突变、BRAF突变、PIK3CA突变、PTEN缺失、AREG和EREG表达以及HER-2扩增在内的许多生物标志物,已被确定用于选择抗EGFR药物的反应者。在这些改变中,KRAS和NRAS突变目前被认为是原发性耐药的最佳预测因素。液体活检有助于分离循环肿瘤DNA,可以研究对抗EGFR单克隆抗体的原发性和获得性耐药,是一种创新方法。然而,应使用高灵敏度技术,以识别与耐药相关的多种基因突变。