Hepatology Unit - Department of Medical & Pediatric Science, University of Catania Policlinic, Via S Sofia 78, 95123, Catania, Italy.
Future Oncol. 2013 Oct;9(10):1533-48. doi: 10.2217/fon.13.171.
Hepatocellular carcinoma (HCC) is now the third leading cause of cancer deathsworldwide and is generally presented at an advanced stage, limiting patients' quality of life. The conventional cytotoxic systemic therapy has proved to be ineffective in HCC, since its induction several decades ago. Today it is possible to use our knowledge of molecular hepatocarcinogenesis to provide a targeted therapy. Sorafenib has demonstrated large improvements in overall survival in HCC. This review describes the molecular mechanisms and potential therapeutic targets, focusing on sorafenib, sunitinib, tivantinib, antiangiogenic agents, and current and future immunotherapies. Thus, it will be necessary in the future to classify HCCs into subgroups according to their genomic and proteomic profiling. The identification of key molecules/receptors/signaling pathways and the assessment of their relevance as potential targets will be the main future challenge potentially influencing response to therapy. Defining molecular targeted agents that are effective for a specific HCC subgroup will hopefully lead to personalized therapy.
肝细胞癌 (HCC) 现已成为全球癌症死亡的第三大主要原因,且通常在晚期出现,限制了患者的生活质量。自几十年前引入以来,传统的细胞毒性全身治疗已被证明对 HCC 无效。如今,我们可以利用对分子肝细胞癌发生的认识来提供靶向治疗。索拉非尼已证明可显著提高 HCC 的总生存率。本文描述了分子机制和潜在的治疗靶点,重点介绍了索拉非尼、舒尼替尼、替沃替尼、抗血管生成药物以及当前和未来的免疫疗法。因此,未来有必要根据 HCC 的基因组和蛋白质组图谱将其分为亚组。确定关键分子/受体/信号通路,并评估其作为潜在靶点的相关性,将是未来的主要挑战,可能会影响对治疗的反应。确定对特定 HCC 亚组有效的分子靶向药物有望带来个性化治疗。