Porta Camillo, Paglino Chiara
Camillo Porta, Medical Oncology and Laboratory of Preclinical Oncology and Experimental Therapies, IRCCS San Matteo University Hospital Foundation, Pavia I-27100, Italy.
World J Hepatol. 2010 Mar 27;2(3):103-13. doi: 10.4254/wjh.v2.i3.103.
Even though Sorafenib has radically changed the natural history of those hepatocellular carcinoma patients who are not amenable for curative treatments, further therapeutic improvements are badly needed. As it was for Sorafenib, our increasingly refined understanding of the complex mechanisms underlying HCC carcinogenesis are the starting point for the future development of such treatments. Presently, a number of molecularly targeted agents are in different stages of development for this once orphan cancer. Indeed, several pathways are presently being explored to identify potentially active drugs, including epidermal growth factor receptor, vascular endothelial growth factor/vascular endothelial growth factor receptors, mammalian target of rapamycin, phosphatidyl-inositol-3-kinase/Akt, insulin growth factor, Aurora kinase, Wnt/β-catenin, retinoic acid receptor and hepatocyte growth factor/C-Met. This review is aimed at addressing the results obtained so far with these newer drugs, also considering the challenges we shall face in the near future, including the issue of response evaluation and identification of predictive/prognostic biomarkers.
尽管索拉非尼已从根本上改变了那些无法接受根治性治疗的肝细胞癌患者的自然病程,但仍迫切需要进一步的治疗改进。正如索拉非尼的情况一样,我们对肝癌发生复杂机制的日益深入理解是此类治疗未来发展的起点。目前,一些分子靶向药物正处于针对这种曾经的罕见癌症的不同开发阶段。事实上,目前正在探索多种途径以识别潜在的活性药物,包括表皮生长因子受体、血管内皮生长因子/血管内皮生长因子受体、雷帕霉素靶蛋白、磷脂酰肌醇-3-激酶/蛋白激酶B、胰岛素生长因子、极光激酶、Wnt/β-连环蛋白、视黄酸受体和肝细胞生长因子/c-Met。本综述旨在阐述这些新型药物迄今所取得的结果,同时也考虑到我们在不久的将来将面临的挑战,包括疗效评估问题以及预测性/预后生物标志物的识别。