Section of Medical Oncology, Department of Surgical and Oncological Sciences, Universita di Palermo, Via del Vespro 129, 90127 Palermo, Italy.
Curr Med Chem. 2014;21(8):966-74. doi: 10.2174/09298673113209990234.
The onset of hepatocellular carcinoma (HCC) is related to the development of non-neoplastic liver disease, such as viral infections and cirrhosis. Even though patients with chronic liver diseases undergo clinical surveillance for early diagnosis of HCC, this cancer is often diagnosed in advanced stage. In this case locoregional treatment is not possible and systemic therapies are the best way to control it. Until now sorafenib, a Raf and multi-kinase inhibitor has been the best, choice to treat HCC systemically. It showed a survival benefit in multicenter phase III trials. However the proper patient setting to treat is not well defined, since the results in Child-Pugh B patients are conflicting. To date various new target drugs are under developed and other biological treatments normally indicated in other malignancies are under investigation also for HCC. These strategies aim to target the different biological pathways implicated in HCC development and progression. The target drugs studied in HCC include anti-VEGF and anti-EGFR monoclonal antibodies, tyrosine kinase inhibitors and mTOR inhibitors. The most important challenge is represented by the best integration of these drugs with standard treatments to achieve improvement in overall survival and quality of life.
肝细胞癌 (HCC) 的发病与非肿瘤性肝病的发展有关,如病毒感染和肝硬化。尽管患有慢性肝病的患者接受临床监测以早期诊断 HCC,但这种癌症通常在晚期诊断。在这种情况下,局部区域治疗是不可能的,系统治疗是控制它的最佳方法。到目前为止,Raf 和多激酶抑制剂索拉非尼一直是治疗 HCC 系统的最佳选择。它在多中心 III 期试验中显示出生存获益。然而,由于 Child-Pugh B 患者的结果存在争议,因此尚未明确最佳的治疗患者人群。迄今为止,正在开发各种新的靶向药物,其他通常用于其他恶性肿瘤的生物治疗也在研究中也用于 HCC。这些策略旨在针对 HCC 发展和进展中涉及的不同生物学途径。在 HCC 中研究的靶向药物包括抗 VEGF 和抗 EGFR 单克隆抗体、酪氨酸激酶抑制剂和 mTOR 抑制剂。最大的挑战是将这些药物与标准治疗最佳整合,以提高总生存率和生活质量。