Division of Medical Oncology, Stanford Clinical Cancer Center, Stanford, California 94305-5826, USA.
J Thorac Oncol. 2010 Jan;5(1):129-39. doi: 10.1097/JTO.0b013e3181c59a60.
Although lung cancer therapy has slowly improved with standard cytotoxic chemotherapy drugs, we have reached an efficacy plateau. The addition of targeted agents, such as those with antiangiogenesis activity, to chemotherapy can improve response and survival outcomes. The first of these agents to gain approval in lung cancer in October 2006 was the antivascular endothelial growth factor antibody, bevacizumab. Small molecule tyrosine kinase inhibitors targeting the vascular endothelial growth factor receptor also have proven activity and are under active investigation. Vascular disrupting agents target existing tumor vasculature leading to tumor necrosis, and are being studied in solid tumors, including lung cancer, both as single agents and in combination with chemotherapy. This article will review these new targeted antiangiogenic and antivascular agents with a focus on their use as lung cancer therapeutics.
虽然肺癌的治疗已经随着标准细胞毒性化疗药物的缓慢进展而有所改善,但我们已经达到了疗效的瓶颈。将靶向药物(如具有抗血管生成活性的药物)添加到化疗中可以提高反应和生存结果。2006 年 10 月,第一个在肺癌中获得批准的药物是抗血管内皮生长因子抗体贝伐珠单抗。针对血管内皮生长因子受体的小分子酪氨酸激酶抑制剂也已被证明具有活性,并正在积极研究中。血管破坏剂针对现有的肿瘤血管,导致肿瘤坏死,正在包括肺癌在内的实体瘤中进行研究,无论是作为单一药物还是与化疗联合使用。本文将重点介绍这些新的靶向抗血管生成和抗血管药物在肺癌治疗中的应用。