Ludwig Center for Cancer Immunotherapy, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Cancer Treat Rev. 2010 May;36(3):235-48. doi: 10.1016/j.ctrv.2009.12.009. Epub 2010 Feb 1.
Because of the poor prognosis for patients with locally advanced and metastatic esophageal, gastroesophageal junction and gastric cancers, increasing attention has focused on the integration of targeted agents into current therapies. The molecular targets of these agents include epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF) or its receptor, cyclooxygenase-2 (COX-2), mammalian target of rapamycin (mTOR) and components and regulators of the cell cycle. In this review article, we briefly discuss pre-clinical data and the rationale for targeting these pathways and summarize the results of clinical trials to-date, including completed and ongoing phase III evaluations.
由于局部晚期和转移性食管、胃食管交界处和胃癌患者的预后较差,因此越来越多的人关注将靶向药物整合到当前的治疗中。这些药物的分子靶点包括表皮生长因子受体(EGFR)、血管内皮生长因子(VEGF)或其受体、环氧化酶-2(COX-2)、雷帕霉素哺乳动物靶点(mTOR)以及细胞周期的组成部分和调节剂。在这篇综述文章中,我们简要讨论了针对这些途径的临床前数据和原理,并总结了迄今为止的临床试验结果,包括已完成和正在进行的 III 期评估。