Hematology-Oncology Division, Department of Hematology Oncology, Hôpital Notre Dame, Centre Hospitalier de l'Université de Montréal, 1560 Sherbrooke Street East, Montréal, QC, H2L 4M1, Canada.
BioDrugs. 2016 Apr;30(2):95-104. doi: 10.1007/s40259-016-0166-5.
Colorectal cancer (CRC) is one of the leading causes of cancer-related mortality worldwide. In the past 2 decades, advances in cancer therapeutics allowed for a remarkable improvement in terms of survival for patients with metastatic CRC. The advent of targeted therapy, coupled with more efficient chemotherapy regimens, was the pillar achievement that contributed to the success of CRC therapy. Cetuximab and panitumumab, monoclonal antibodies targeting the epidermal growth factor receptor pathway, are the focus of this review since their mechanism of action and efficiency are closely related to the mutational status of a predictive biomarker, the Kristen rat Sarcoma viral oncogene (KRAS). More recently, another biomarker, the neuroblastoma rat sarcoma viral oncogene (NRAS), was found to be as valuable for the refinement of this targeted therapy. The arguments for the use of extended analysis of the RAS gene are thoroughly reviewed because they directly affect the choice of targeted agents and potentially the choice of backbone chemotherapy.
结直肠癌(CRC)是全球癌症相关死亡的主要原因之一。在过去的 20 年中,癌症治疗的进步使得转移性 CRC 患者的生存率得到了显著提高。靶向治疗的出现,加上更有效的化疗方案,是 CRC 治疗成功的主要成就。本文重点介绍针对表皮生长因子受体途径的单克隆抗体西妥昔单抗和帕尼单抗,因为它们的作用机制和疗效与预测生物标志物的突变状态密切相关,即 Kirsten 大鼠肉瘤病毒癌基因(KRAS)。最近,另一个生物标志物神经母细胞瘤大鼠肉瘤病毒癌基因(NRAS)也被发现对这种靶向治疗的精细化具有重要价值。因此,本文对 RAS 基因的扩展分析的使用进行了深入的审查,因为它们直接影响靶向药物的选择,并且可能影响基础化疗药物的选择。