Rinninella Emanuele, Cerrito Lucia, Spinelli Irene, Cintoni Marco, Mele Maria Cristina, Pompili Maurizio, Gasbarrini Antonio
Internal Medicine and Gastroenterology Unit, Gastroenterology Area, Fondazione Policlinico Universitario Agostino Gemelli, Catholic University of Sacred Heart, Rome, Italy.
Clinical Nutrition Unit, Gastroenterology Area, Fondazione Policlinico Universitario Agostino Gemelli, Catholic University of Sacred Heart, Rome, Italy.
J Clin Transl Hepatol. 2017 Sep 28;5(3):235-248. doi: 10.14218/JCTH.2017.00002. Epub 2017 Jun 8.
Hepatocarcinogenesis is a multistep process, heralded by abnormalities in cell differentiation and proliferation and sustained by an aberrant neoangiogenesis. Understanding the underlying molecular pathogenesis leading to hepatocellular carcinoma is a prerequisite to develop new drugs that will hamper or block the steps of these pathways. As hepatocellular carcinoma has higher arterial vascularization than normal liver, this could be a good target for novel molecular therapies. Introduction of the antiangiogenic drug sorafenib into clinical practice since 2008 has led to new perspectives in the management of this tumor. The importance of this drug lies not only in the modest gain of patients' survival, but in having opened a roadmap towards the development of new molecules and targets. Unfortunately, after the introduction of sorafenib, during the last years, a wide number of clinical trials on antiangiogenic therapies failed in achieving significant results. However, many of these trials are still ongoing and promise to improve overall survival and progression-free survival. A recent clinical trial has proven regorafenib effective in patients showing tumor progression under sorafenib, thus opening new interesting therapeutic perspectives. Many other expectations have been borne from the discovery of the immune checkpoint blockade, already known in other solid malignancies. Furthermore, a potential role in hepatocellular carcinoma therapy may derive from the use of branched-chain amino acids and of nutritional support. This review analyses the biomolecular pathways of hepatocellular carcinoma and the ongoing studies, the actual evidence and the future perspectives concerning drug therapy in this open field.
肝癌发生是一个多步骤过程,以细胞分化和增殖异常为先导,并由异常的新生血管生成维持。了解导致肝细胞癌的潜在分子发病机制是开发能够阻碍或阻断这些途径步骤的新药的先决条件。由于肝细胞癌的动脉血管化程度高于正常肝脏,这可能是新型分子疗法的一个良好靶点。自2008年抗血管生成药物索拉非尼引入临床实践以来,为这种肿瘤的治疗带来了新的前景。这种药物的重要性不仅在于适度延长了患者的生存期,还在于为新分子和靶点的开发开辟了道路。不幸的是,在引入索拉非尼后的最近几年里,大量抗血管生成疗法的临床试验未能取得显著成果。然而,许多此类试验仍在进行中,并有望改善总生存期和无进展生存期。最近一项临床试验已证明瑞戈非尼对在索拉非尼治疗下出现肿瘤进展的患者有效,从而开辟了新的有趣治疗前景。免疫检查点阻断在其他实体恶性肿瘤中已为人所知,其发现也带来了许多其他期望。此外,支链氨基酸的使用和营养支持在肝细胞癌治疗中可能具有潜在作用。本综述分析了肝细胞癌的生物分子途径以及正在进行的研究、实际证据和该开放领域药物治疗的未来前景。