Torrecilla S, Llovet J M
Liver Cancer Translational Research Laboratory, Barcelona-Clínic Liver Cancer Group, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic de Barcelona, Universitat de Barcelona (UB), Barcelona, Catalonia, Spain.
Liver Cancer Translational Research Laboratory, Barcelona-Clínic Liver Cancer Group, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic de Barcelona, Universitat de Barcelona (UB), Barcelona, Catalonia, Spain; Mount Sinai Liver Cancer Program, Division of Liver Diseases, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, Madison avenue 1425, 11F-70, Box 1123, 10029 New York, USA; Institució Catalana de Recerca i Estudis Avançats, Barcelona, Catalonia, Spain.
Clin Res Hepatol Gastroenterol. 2015 Sep;39 Suppl 1:S80-5. doi: 10.1016/j.clinre.2015.06.016. Epub 2015 Jul 20.
Hepatocellular carcinoma (HCC) is a major health problem. Mortality owing to liver cancer has increased in the past 20 years, with recent studies reporting an incidence of 780,000 cases/year. Most patients with hepatocellular carcinoma are still diagnosed at intermediate or advanced disease stages, where curative approaches are often not feasible. Among the treatment options available, the molecular targeted agent sorafenib is able to significantly increase overall survival in these patients. Afterwards, up to 7 randomized phase III clinical trials investigating other molecular therapies in the first-line and second-line settings have failed to improve survival. Potential reasons for this include intertumor heterogeneity, issues with trial design and a lack of predictive biomarkers of response. Advance in our knowledge of the human genome has provided a comprehensive picture of commonly mutated genes in patients with HCC including mutations in the TERT promoter, CTNNB1, TP53 and ARID1A along with other amplifications (FGF19, VEGFA) or homozygous deletions (p16) as the most frequent alterations. This knowledge points toward specific drivers as candidate for druggable therapies. Thus, progressive implementation of proof-of-concept and enrichment might improve results in clinical trials testing of molecular targeted agents. Ultimately, these studies are aimed at long-term to improve current standards of care and influenced clinical decision-making and practice guidelines.
肝细胞癌(HCC)是一个重大的健康问题。在过去20年中,肝癌导致的死亡率有所上升,最近的研究报告显示其发病率为每年78万例。大多数肝细胞癌患者仍在疾病的中期或晚期被诊断出来,而在这些阶段,治愈性方法往往不可行。在现有的治疗选择中,分子靶向药物索拉非尼能够显著提高这些患者的总生存率。此后,多达7项在一线和二线治疗环境中研究其他分子疗法的随机III期临床试验未能提高生存率。其潜在原因包括肿瘤间的异质性、试验设计问题以及缺乏反应预测生物标志物。我们对人类基因组认识的进步提供了一幅关于HCC患者常见突变基因的全面图景,包括TERT启动子、CTNNB1、TP53和ARID1A的突变,以及其他扩增(FGF19、VEGFA)或纯合缺失(p16)作为最常见的改变。这些知识指向特定的驱动因素作为可药物治疗的候选对象。因此,逐步实施概念验证和富集可能会改善分子靶向药物临床试验的结果。最终,这些研究旨在长期改善当前的护理标准,并影响临床决策和实践指南。