Department of Gastroenterology and Hepatology, Kinki University School of Medicine, Osaka, Japan.
Dig Dis. 2011;29(3):289-302. doi: 10.1159/000327562. Epub 2011 Aug 9.
In recent years, molecular-targeted agents have been used clinically to treat various malignant tumors. In May 2009, sorafenib (Nexavar®) was approved in Japan for 'unresectable hepatocellular carcinoma (HCC)', and was the first molecular-targeted agent for use in HCC. To date, sorafenib is the only molecular-targeted agent whose survival benefit has been demonstrated in two global phase III randomized controlled trials, and has now been approved worldwide. Phase III clinical trials of other molecular-targeted agents comparing them with sorafenib as first-line treatment agents are now ongoing. Those agents target the vascular endothelial growth factor, platelet-derived growth factor receptors, as well as target the epidermal growth factor receptor, insulin-like growth factor receptor and mammalian target of rapamycin, in addition to other molecules targeting other components of the signal transduction pathways. This review outlines the main pathways involved in the development and progression of HCC and the agents that target these pathways. Finally, current status and future perspective will also be discussed.
近年来,分子靶向药物已被临床用于治疗各种恶性肿瘤。2009 年 5 月,索拉非尼(多吉美®)在日本被批准用于“不可切除的肝细胞癌(HCC)”,成为首个用于 HCC 的分子靶向药物。迄今为止,索拉非尼是唯一在两项全球 III 期随机对照临床试验中显示生存获益的分子靶向药物,现已在全球范围内获得批准。目前正在进行其他分子靶向药物的 III 期临床试验,将其与索拉非尼作为一线治疗药物进行比较。这些药物的靶点包括血管内皮生长因子、血小板衍生生长因子受体,以及表皮生长因子受体、胰岛素样生长因子受体和哺乳动物雷帕霉素靶蛋白,此外还有针对信号转导通路其他成分的其他分子的靶点。本文综述了 HCC 发生和进展中涉及的主要途径以及针对这些途径的药物。最后,还讨论了当前的状况和未来的展望。