Department of Medicine, Division of Hematology and Oncology, The Ohio State University-Arthur James Cancer Hospital, Columbus, OH 43210-1240, USA.
Clin Colorectal Cancer. 2009 Jul;8(3):135-40. doi: 10.3816/CCC.2009.n.022.
Colorectal cancer is a significant healthcare problem in the United States, with meaningful improvement in survival over the past few years. Much of that improvement is attributable to the availability of molecularly targeted therapies, such as inhibitors of the vascular endothelial growth factor (bevacizumab) and epidermal growth factor receptor (cetuximab and panitumumab), in addition to active cytotoxic agents. KRAS mutations have long been described to play an adverse prognostic role in colorectal cancer. KRAS is downstream from EGFR, and oncogenic mutations will yield a constitutively active protein that will override EGFR control of downstream signaling. Such mutations in KRAS would therefore confer resistance to anti-EGFR antibodies. The cumulative results of several trials incorporating more than a thousand patients in studies of cetuximab and panitumumab confirm that the presence of KRAS mutation in tumors is highly predictive of resistance to anti-EGFR therapy. These findings are likely to change the landscape of metastatic CRC treatment by providing an improved patient-tailored approach.
结直肠癌是美国一个重大的医疗保健问题,在过去几年中,其生存率有了显著提高。这种改善在很大程度上归因于分子靶向治疗药物的出现,如血管内皮生长因子(bevacizumab)和表皮生长因子受体(cetuximab 和 panitumumab)抑制剂,以及活性细胞毒性药物。KRAS 突变长期以来一直被描述为结直肠癌的不良预后因素。KRAS 位于 EGFR 的下游,致癌突变会产生一种持续激活的蛋白,从而推翻 EGFR 对下游信号的控制。因此,KRAS 中的这种突变会导致对抗 EGFR 抗体的耐药性。几项临床试验的累积结果表明,在 cetuximab 和 panitumumab 的研究中,超过 1000 名患者的研究证实,肿瘤中 KRAS 突变的存在高度预测对 EGFR 治疗的耐药性。这些发现可能通过提供一种改进的个体化治疗方法来改变转移性 CRC 的治疗格局。