Department of Precision Medicine, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Gastroenterology Unit, Ospedale Umberto I, Nocera Inferiore, Italy.
Cancer Treat Rev. 2020 Jun;86:102023. doi: 10.1016/j.ctrv.2020.102023. Epub 2020 Apr 13.
Colorectal cancer (CRC) represents a global health problem, being one of the most diagnosed and aggressive tumors. Cetuximab and panitumumab monoclonal antibodies (mAbs) in combination with chemotherapy are an effective strategy for patients with RAS Wild Type (WT) metastatic colorectal cancer (mCRC). However, tumors are often unresponsive or develop resistance. In the last years, molecular alterations in principal oncogenes (RAS, BRAF, PI3KCA, PTEN) in the downstream pathway of the epidermal growth factor receptor (EGFR) and in other receptors (HER2, MET) that converge on MAPK-ERK signalling have been identified as novel mechanisms of resistance to anti-EGFR strategies. However, further efforts are needed to better stratify CRCs and ensure more individualized treatments. Herein, we describe the consolidated molecular drivers of resistance and the therapeutic strategies available so far, with an overview on potential biomarkers of response that could be integrated in clinical practice.
结直肠癌(CRC)是一个全球性的健康问题,是最常见和侵袭性的肿瘤之一。西妥昔单抗和帕尼单抗单克隆抗体(mAbs)联合化疗是 RAS 野生型(WT)转移性结直肠癌(mCRC)患者的有效治疗策略。然而,肿瘤常常无反应或产生耐药性。近年来,表皮生长因子受体(EGFR)下游途径中的主要癌基因(RAS、BRAF、PI3KCA、PTEN)和其他受体(HER2、MET)中的分子改变已被确定为抗 EGFR 策略耐药的新机制。然而,仍需要进一步努力来更好地对 CRC 进行分层,并确保更个体化的治疗。在此,我们描述了耐药的综合分子驱动因素和迄今为止可用的治疗策略,并概述了可能整合到临床实践中的潜在反应生物标志物。