Suppr超能文献

转移性结直肠癌中表皮生长因子受体的耐药性:还有哪些需要解决?

Resistance to anti-epidermal growth factor receptor in metastatic colorectal cancer: What does still need to be addressed?

机构信息

Department of Precision Medicine, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.

Gastroenterology Unit, Ospedale Umberto I, Nocera Inferiore, Italy.

出版信息

Cancer Treat Rev. 2020 Jun;86:102023. doi: 10.1016/j.ctrv.2020.102023. Epub 2020 Apr 13.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验