Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
J Hematol Oncol. 2012 Jun 18;5:31. doi: 10.1186/1756-8722-5-31.
Contemporary advancements have had little impact on the treatment of gastric cancer (GC), the world's second highest cause of cancer death. Agents targeting human epidermal growth factor receptor mediated pathways have been a common topic of contemporary cancer research, including monoclonal antibodies (mAbs) and receptor tyrosine kinase inhibitors (TKIs). Trastuzumab is the first target agent evidencing improvements in overall survival in HER2-positive (human epidermal growth factor receptor 2) gastric cancer patients. Agents targeting vascular epithelial growth factor (VEGF), mammalian target of rapamycin (mTOR), and other biological pathways are also undergoing clinical trials, with some marginally positive results. Effective targeted therapy requires patient selection based on predictive molecular biomarkers. Most phase III clinical trials are carried out without patient selection; therefore, it is hard to achieve personalized treatment and to monitor patient outcome individually. The trend for future clinical trials requires patient selection methods based on current understanding of GC biology with the application of biomarkers.
尽管现代医学取得了诸多进展,但胃癌(GC)的治疗仍然举步维艰,胃癌是全球第二大癌症死因。针对人类表皮生长因子受体介导途径的药物一直是当代癌症研究的热门课题,包括单克隆抗体(mAbs)和受体酪氨酸激酶抑制剂(TKIs)。曲妥珠单抗是首个能够改善人表皮生长因子受体 2(HER2)阳性胃癌患者总生存期的靶向药物。针对血管内皮生长因子(VEGF)、雷帕霉素靶蛋白(mTOR)和其他生物途径的药物也正在进行临床试验,部分结果呈阳性。有效的靶向治疗需要根据预测性分子生物标志物选择患者。大多数 III 期临床试验在没有患者选择的情况下进行;因此,很难实现个体化治疗,也很难单独监测患者的结果。未来临床试验的趋势需要基于对 GC 生物学的当前理解,结合生物标志物的应用,选择患者的方法。