Thomas Melanie B, Abbruzzese James L
Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, 77030, USA.
J Clin Oncol. 2005 Nov 1;23(31):8093-108. doi: 10.1200/JCO.2004.00.1537.
Hepatocellular cancer (HCC) is the fifth most common solid tumor worldwide, accounting for 500,000 new cases annually. Although less common in the United States, HCC is expected to increase in incidence over the next two decades largely because of the prevalence of hepatitis C virus infection. A majority of patients present with advanced disease and are not candidates for liver transplantation, surgical resection, or regional therapy. In 60% to 80% of patients with HCC, treatment is complicated by underlying liver cirrhosis and hepatic dysfunction. Systemic treatments are minimally effective, can have significant toxicity, and have not been shown to improve patient survival. New approaches targeting molecular abnormalities specific to HCC are needed to improve patient outcome. This review summarizes the state of knowledge of those key aspects of the molecular pathogenesis of HCC that may represent rational therapeutic targets in this disease. Relevant preclinical and clinical information on novel compounds directed toward abnormalities in HCC is reviewed.
肝细胞癌(HCC)是全球第五大常见实体瘤,每年新增病例达50万例。尽管在美国HCC的发病率较低,但预计在未来二十年中其发病率将上升,这主要归因于丙型肝炎病毒感染的流行。大多数患者就诊时已处于疾病晚期,不适合进行肝移植、手术切除或区域治疗。在60%至80%的HCC患者中,治疗因潜在的肝硬化和肝功能障碍而变得复杂。全身治疗效果甚微,可能具有显著毒性,且尚未显示能改善患者生存率。需要针对HCC特异性分子异常的新方法来改善患者预后。本综述总结了HCC分子发病机制中那些可能代表该疾病合理治疗靶点的关键方面的知识现状。还综述了针对HCC异常的新型化合物的相关临床前和临床信息。