Impact of hepatitis C virus eradication on hepatocellular carcinogenesis

被引:68
|
作者
Li, Darrick K. [1 ]
Chung, Raymond T. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Med, Div Gastroenterol, Ctr Liver, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
chronic hepatitis C; cirrhosis; direct-acting antivirals; hepatocellular carcinoma; risk factors; sustained virological response; SUSTAINED VIROLOGICAL RESPONSE; TREATMENT-NAIVE PATIENTS; GENOTYPE; PEGYLATED INTERFERON; CARCINOMA DEVELOPMENT; CURATIVE TREATMENT; COST-EFFECTIVENESS; CANCER STATISTICS; GENE-EXPRESSION; PLUS RIBAVIRIN;
D O I
10.1002/cncr.29528
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death in the world. Infection with hepatitis C virus (HCV) represents one of the most common risk factors for HCC development, and cases of HCV-related complications have been rising over the last 2 decades. Although the standard for HCV therapy has been interferon (IFN)-based for many years, the therapeutic revolution spurred by the development of direct-acting antivirals (DAAs) promises to usher in a new era in which chronic HCV becomes a rare disease. On the basis of long-term follow-up of patients experiencing IFN-based sustained virological responses (SVRs), it can be expected that rates of HCV-associated HCC will decrease significantly after the widespread adoption of DAAs, but there remains a persistent risk for HCC even among some patients with advanced fibrosis who have achieved SVR. As such, individuals treated for HCV with advanced fibrosis should continue to be screened regularly for HCC after SVR. Furthermore, as the population of SVR patients grows, it will become imperative to accurately identify those individuals at high risk for developing HCC, appropriately allocate resources for screening, and consider cost-effective chemopreventive strategies. Risk factors include preexisting advanced fibrosis/cirrhosis, older age, diabetes mellitus, and ethanol use. In addition, laboratory biomarkers and genetic signatures are currently being identified that not only predict the likelihood of HCC development in SVR patients but also may serve as dynamic indicators of therapeutic response. Cancer 2015;121:2874-2882. (c) 2015 American Cancer Society.
引用
收藏
页码:2874 / 2882
页数:9
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