Anestis Aristomenis, Zoi Ilianna, Karamouzis Michalis V
Molecular Oncology Unit, Department of Biological Chemistry, 'Laiko' General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
First Department of Internal Medicine, 'Laiko' General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Ann Transl Med. 2018 Jun;6(12):247. doi: 10.21037/atm.2018.04.42.
Despite the advances in systemic chemotherapy, gastric adenocarcinoma (GC) remains the third most common cause of cancer-related deaths with poor prognosis. The heterogeneity of GC indicates that novel biomarkers should be established in order to further classify tumors and develop individual targeted therapies. High-quality preclinical and clinical research has demonstrated that growth factor (HGF)-hepatocyte growth factor receptor (c-Met) pathway plays a pivotal role on the growth, survival and invasiveness of GC. In particular, aberrant activation of HGF/c-Met signaling pathway has been associated with poor clinical outcomes, suggesting the therapeutic potential of c-Met. This has stimulated the development and evaluation of a number of c-Met targeted agents in an advance disease setting. In this review, we summarize the current state of the art in the advances on the inhibition of c-Met pathway, with particular emphasis on the clinical testing of c-Met targeted therapeutic agents. Furthermore, we discuss the challenges facing the incorporation of c-Met targeted agents in randomized trials, with the idea that the definition of the appropriate genetic and molecular context for the use of these agents remains the priority.
尽管全身化疗取得了进展,但胃腺癌(GC)仍是癌症相关死亡的第三大常见原因,预后较差。GC的异质性表明,应建立新的生物标志物,以便进一步对肿瘤进行分类并开发个体化的靶向治疗。高质量的临床前和临床研究表明,生长因子(HGF)-肝细胞生长因子受体(c-Met)通路在GC的生长、存活和侵袭中起关键作用。特别是,HGF/c-Met信号通路的异常激活与不良临床结果相关,提示了c-Met的治疗潜力。这刺激了多种c-Met靶向药物在晚期疾病环境中的开发和评估。在本综述中,我们总结了c-Met通路抑制方面的最新进展,特别强调了c-Met靶向治疗药物的临床试验。此外,我们讨论了将c-Met靶向药物纳入随机试验所面临的挑战,认为确定使用这些药物的合适基因和分子背景仍然是首要任务。