1st Department of Medical Oncology, Metropolitan Hospital, Athens, Greece.
Cancer Treat Rev. 2011 May;37(3):221-33. doi: 10.1016/j.ctrv.2010.07.008. Epub 2010 Sep 29.
The KRAS oncogene has been extensively studied for more than three decades, however, it is only recently that it attained a central role in the clinical decision-making process for the practicing oncologist. Recently, based on retrospective analyses of large randomized clinical trials, the use of anti-epidermal growth factor (EGFR) monoclonal antibodies, cetuximab and panitumumab, was restricted to patients with metastatic colorectal cancer that carry the "wild-type"KRAS genotype. Challenges remain in the laboratory implementation of KRAS mutational testing and the clinical application of the test for treatment planning. This review attempts to offer a global view of KRAS biology, its functional role in cell signaling, mechanisms of resistance to anti-EGFR agents and its predictive potential in metastatic colorectal cancer. We also survey the growing list of candidate biomarkers that may shortly supplement KRAS in routine clinical patient stratification. Finally, we discuss practical aspects of KRAS testing that may be useful for those involved in mutational screening in their centers. This general overview of KRAS for clinical oncology practice aims to assist in data interpretation and offer insight into potential pitfalls of mutational testing. KRAS is a prime example of how translational research can fulfill the promises of personalized medicine for tailoring treatment to match the underlying tumor biology.
KRAS 癌基因已经被广泛研究了三十多年,但直到最近,它才在临床肿瘤学家的决策过程中发挥核心作用。最近,基于大型随机临床试验的回顾性分析,抗表皮生长因子(EGFR)单克隆抗体,西妥昔单抗和帕尼单抗的使用被限制在携带“野生型”KRAS 基因型的转移性结直肠癌患者中。在实验室实施 KRAS 基因突变检测和将该检测用于治疗计划方面仍然存在挑战。本综述试图提供 KRAS 生物学的全球视角,其在细胞信号转导中的功能作用,对 EGFR 抑制剂的耐药机制及其在转移性结直肠癌中的预测潜力。我们还调查了可能很快在常规临床患者分层中补充 KRAS 的不断增长的候选生物标志物列表。最后,我们讨论了 KRAS 检测的实际方面,这可能对那些在其中心进行突变筛选的人有用。这篇临床肿瘤学实践的 KRAS 综述旨在帮助解释数据,并深入了解突变检测的潜在陷阱。KRAS 是转化研究如何为个性化医疗提供帮助,从而根据肿瘤生物学基础来定制治疗的一个很好的例子。