van Krieken J H J M, Jung A, Kirchner T, Carneiro F, Seruca R, Bosman F T, Quirke P, Fléjou J F, Plato Hansen T, de Hertogh G, Jares P, Langner C, Hoefler G, Ligtenberg M, Tiniakos D, Tejpar S, Bevilacqua G, Ensari A
Department of Pathology, Radboud University Nijmegen Medical Centre, Nijmegen, 6500, HB, The Netherlands.
Virchows Arch. 2008 Nov;453(5):417-31. doi: 10.1007/s00428-008-0665-y. Epub 2008 Sep 18.
Novel therapeutic agents targeting the epidermal growth factor receptor (EGFR) have improved outcomes for patients with colorectal carcinoma. However, these therapies are effective only in a subset of patients. Activating mutations in the KRAS gene are found in 30-40% of colorectal tumors and are associated with poor response to anti-EGFR therapies. Thus, KRAS mutation status can predict which patient may or may not benefit from anti-EGFR therapy. Although many diagnostic tools have been developed for KRAS mutation analysis, validated methods and standardized testing procedures are lacking. This poses a challenge for the optimal use of anti-EGFR therapies in the management of colorectal carcinoma. Here we review the molecular basis of EGFR-targeted therapies and the resistance to treatment conferred by KRAS mutations. We also present guideline recommendations and a proposal for a European quality assurance program to help ensure accuracy and proficiency in KRAS mutation testing across the European Union.
针对表皮生长因子受体(EGFR)的新型治疗药物改善了结直肠癌患者的治疗效果。然而,这些疗法仅对一部分患者有效。在30%-40%的结直肠癌肿瘤中发现了KRAS基因的激活突变,这些突变与抗EGFR疗法的疗效不佳相关。因此,KRAS突变状态可以预测哪些患者可能从抗EGFR治疗中获益,哪些患者可能无法获益。尽管已经开发了许多用于KRAS突变分析的诊断工具,但缺乏经过验证的方法和标准化的检测程序。这对在结直肠癌治疗中最佳使用抗EGFR疗法构成了挑战。在此,我们综述了EGFR靶向治疗的分子基础以及KRAS突变导致的治疗耐药性。我们还提出了指南建议以及一项欧洲质量保证计划提案,以帮助确保在欧盟范围内KRAS突变检测的准确性和熟练度。