Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1475 NW 12th Avenue, D8-4, Miami, FL 33136, USA.
Expert Rev Anticancer Ther. 2010 Oct;10(10):1577-87. doi: 10.1586/era.10.141.
Lung cancer research has incorporated molecular medicine into the management of this disease during the last 5 years. Several novel tumorigenesis pathways associated with lung cancer development and proliferation have been discovered and further developed as targets. The idea behind this is to deliver individualized therapy for each patient based on his/her tumor phenotype, which may involve the overexpression or lack of certain proteins, receptors, mutations and other factors. To date, many of these characteristics have been shown to have a potential role as prognostic or predictive biomarkers, with most of the available data being obtained from retrospective analyses, various laboratory platforms, and data sets used for comparison. However, well-designed prospective randomized clinical trials are underway to validate the significance and future role of these novel biomarkers, allowing us to sort out the best personalized management for an individual with lung cancer diagnosis. Nevertheless, one of these features, the EGF receptor (EGFR) gene mutation, has emerged as a prognostic and strongly predictive biomarker when EGFR inhibition is used as a therapy for tumors that harbor the mutation. Our article displays the most recently developed data related to this biomarker and what have we learned based on the analyses of clinical trials that have studied different agents in the clinical arena.
在过去的 5 年中,肺癌研究已经将分子医学纳入了这种疾病的治疗中。已经发现了与肺癌发展和增殖相关的几个新的肿瘤发生途径,并进一步将其作为靶点进行开发。其背后的想法是根据每个患者的肿瘤表型为其提供个体化治疗,这可能涉及某些蛋白质、受体、突变和其他因素的过表达或缺乏。迄今为止,这些特征中的许多已被证明具有作为预后或预测生物标志物的潜力,大多数可用数据是从回顾性分析、各种实验室平台以及用于比较的数据集中获得的。然而,正在进行精心设计的前瞻性随机临床试验,以验证这些新型生物标志物的意义和未来作用,从而使我们能够为肺癌患者制定最佳的个性化治疗方案。然而,当 EGFR 抑制作为携带突变的肿瘤的治疗方法时,表皮生长因子受体(EGFR)基因突变已成为一种预后和强预测生物标志物。我们的文章展示了与该生物标志物相关的最新开发数据,以及我们根据在临床领域研究不同药物的临床试验分析中所学到的内容。