Pohl Michael, Schmiegel Wolff
Department of Medicine, Universitx00E4;tsklinikum Knappschaftskrankenhaus, Bochum, Germany.
Dig Dis. 2016;34(5):574-9. doi: 10.1159/000445267. Epub 2016 Jun 22.
Colorectal cancer (CRC) is the third most common cancer type in Western countries. Significant progress has been made in the last decade in the therapy of metastatic CRC (mCRC) with a median overall survival (OS) of patients exceeding 30 months. The integration of biologic targeted therapies and anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (MABs) in the treatment of patients with genomically selected all-RAS wild-type mCRC leads to a significant progress in advanced incurable disease state. After the introduction of the anti-VEGF MAB bevacizumab, the FDA approved with ramucirumab the second antiangiogenic MAB for the mCRC treatment. Further new drugs are on the horizon and new diagnostic tools will be introduced soon.
Molecular heterogeneity of mCRC has been recognized as pivotal in the evolution of clonal populations during anti-EGFR therapies. Mutations in RAS genes predict a lack of response to anti-EGFR MABs. Mutations in the mitogen-activated protein kinase-phosphoinositide 3-kinase pathways like BRAF or PIK3CA mutations or HER2/ERBB2 or MET amplifications bypass EGFR signaling and also may confer resistance to anti-EGFR MABs. HER2/ERBB2 amplification is a further driver of resistance to anti-EGFR MABs in mCRC. The phase II study of HER2 Amplification for Colo-Rectal Cancer Enhanced Stratification (HERACLES) discovers that a dual HER2-targeted therapy may be an option for HER2-amplified mCRC. The mismatch repair deficiency predicts responsiveness to an immune checkpoint blockade with the anti-PD-1 immune checkpoint inhibitor pembrolizumab.
The understanding of primary (de novo) and secondary (acquired) resistance to anti-EGFR therapies, new targeted therapies, immuno-oncology and about predictive biomarkers in mCRC is guiding the development of rational therapeutic strategies. Combinations of targeted therapies are necessary to effectively treat drug-resistant cancers. Liquid biopsy is an upcoming new tool in the primary diagnosis and follow-up analysis of mutations in circulating tumor DNA.
结直肠癌(CRC)是西方国家第三大常见癌症类型。在过去十年中,转移性结直肠癌(mCRC)的治疗取得了显著进展,患者的中位总生存期(OS)超过30个月。生物靶向治疗和抗表皮生长因子受体(EGFR)单克隆抗体(MABs)在基因组选择的全RAS野生型mCRC患者治疗中的整合,在晚期不可治愈疾病状态方面取得了显著进展。在抗VEGF单克隆抗体贝伐单抗推出后,美国食品药品监督管理局(FDA)批准了雷莫西尤单抗作为第二种用于mCRC治疗的抗血管生成单克隆抗体。更多新药即将问世,新的诊断工具也将很快推出。
mCRC的分子异质性已被认为是抗EGFR治疗期间克隆群体演变的关键因素。RAS基因中的突变预示着对抗EGFR单克隆抗体缺乏反应。丝裂原活化蛋白激酶-磷脂酰肌醇3-激酶途径中的突变,如BRAF或PIK3CA突变或HER2/ERBB2或MET扩增,绕过EGFR信号传导,也可能导致对抗EGFR单克隆抗体产生耐药性。HER2/ERBB2扩增是mCRC中抗EGFR单克隆抗体耐药的另一个驱动因素。结直肠癌HER2扩增增强分层的II期研究(HERACLES)发现,双重HER2靶向治疗可能是HER2扩增的mCRC的一种选择。错配修复缺陷预示着对抗程序性死亡蛋白1(PD-1)免疫检查点抑制剂派姆单抗的免疫检查点阻断有反应。
对mCRC中抗EGFR治疗的原发性(新发)和继发性(获得性)耐药、新的靶向治疗、免疫肿瘤学以及预测生物标志物的理解,正在指导合理治疗策略的制定。靶向治疗的联合应用对于有效治疗耐药癌症是必要的。液体活检是循环肿瘤DNA突变的原发性诊断和随访分析中即将出现的新工具。