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慢性丙型肝炎病毒感染患者使用达卡他韦和阿舒瑞韦实现持续病毒学应答后发生肝细胞癌

Hepatocellular Carcinoma after Achievement of Sustained Viral Response with Daclatasvir and Asunaprevir in Patients with Chronic Hepatitis C Virus Infection.

作者信息

Ida Hiroshi, Hagiwara Satoru, Kono Masashi, Minami Tomohiro, Chishina Hirokazu, Arizumi Tadaaki, Takita Masahiro, Yada Norihisa, Minami Yasunori, Ueshima Kazuomi, Nishida Naoshi, Kudo Masatoshi

机构信息

Department of Gastroenterology and Hepatology, Faculty of Medicine, Kindai University, Osaka-Sayama, Japan.

出版信息

Dig Dis. 2017;35(6):565-573. doi: 10.1159/000480183. Epub 2017 Oct 17.

Abstract

BACKGROUND

Interferon-based antiviral therapies against hepatitis C virus (HCV) infection have been shown to reduce the incidence of hepatocellular carcinoma (HCC) in patients with sustained viral response (SVR). Recently, direct-acting antivirals (DAAs) have been proven to be much more effective in achieving SVR than interferon-based therapies. However, whether DAAs can efficiently prevent the occurrence of HCC after SVR remains controversial. To clarify this issue, we analyzed the clinical features of patients in whom HCC developed after achievement of SVR with DAAs for chronic HCV infection.

SUMMARY

Among patients who achieved SVR with daclatasvir and asunaprevir (n = 100), HCC developed in 17 patients (HCC group; n = 17) and did not develop in 83 patients (non-HCC group; n = 83) during a mean observation period of 15 months. A multivariate Cox proportional hazards analysis identified past history of HCC and male sex as significant risk factors for the emergence of HCC after DAAs. Sixteen cases with HCC after DAAs were in the very early or early stage (16/17, 94.1%), and one case was in the advanced stage (1/17, 5.9%) with portal venous tumor thrombus. Radiofrequency ablation and/or transarterial chemoembolization were performed in most cases as curative therapy (16/17, 94.1%). Key Messages: SVR by DAAs did not completely prevent the occurrence of HCC. However, even if HCC did develop after SVR, curative anticancer therapy was applicable in most cases.

摘要

背景

基于干扰素的抗丙型肝炎病毒(HCV)感染抗病毒疗法已被证明可降低获得持续病毒学应答(SVR)患者的肝细胞癌(HCC)发病率。最近,直接抗病毒药物(DAA)已被证明在实现SVR方面比基于干扰素的疗法更有效。然而,DAA在SVR后能否有效预防HCC的发生仍存在争议。为阐明这一问题,我们分析了慢性HCV感染患者使用DAA实现SVR后发生HCC的患者的临床特征。

总结

在使用达卡他韦和阿苏普瑞韦实现SVR的患者(n = 100)中,在平均15个月的观察期内,17例患者发生了HCC(HCC组;n = 17),83例患者未发生HCC(非HCC组;n = 83)。多因素Cox比例风险分析确定HCC既往史和男性为DAA治疗后发生HCC的显著风险因素。DAA治疗后发生HCC的16例患者处于极早期或早期阶段(16/17,94.1%),1例患者处于晚期(1/17,5.9%)并伴有门静脉肿瘤血栓形成。大多数病例采用射频消融和/或经动脉化疗栓塞作为根治性治疗(16/17,94.1%)。关键信息:DAA实现的SVR不能完全预防HCC的发生。然而,即使在SVR后发生了HCC,大多数情况下仍可应用根治性抗癌治疗。

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