Ogasawara Nobuhiko, Saitoh Satoshi, Akuta Norio, Fujiyama Shunichiro, Kawamura Yusuke, Sezaki Hitomi, Hosaka Tetsuya, Kobayashi Masahiro, Suzuki Fumitaka, Suzuki Yoshiyuki, Arase Yasuji, Ikeda Kenji, Kumada Hiromitsu
Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan.
Hepatol Res. 2019 Dec;49(12):1441-1450. doi: 10.1111/hepr.13418. Epub 2019 Oct 9.
The long-term effects of sustained virologic response (SVR) to antiviral therapy on the risk of liver complications, such as exacerbation of esophageal varices (EV), hepatocellular carcinoma (HCC), malignant lymphoma, and liver-related and overall death in hepatitis C virus (HCV)-infected patients with liver cirrhosis are not fully known.
These risks were evaluated during long-term follow up of 457 patients with HCV-related Child-Pugh Class A liver cirrhosis without history of HCC.
The respective cumulative 5- and 10-year rates of EV exacerbation were 2.0% and 3.1%. Multivariate analysis identified the presence of EVs, thrombocytopenia at baseline. and alcohol intake as significant independent predictors of EV exacerbation before and after SVR. The cumulative 5- and 10-year rates of HCC were 6.8% and 10.2%, respectively. Male sex and the presence of EV were significant independent determinants of HCC before and after SVR. Although the cumulative 5-year HCC recurrence rate was 49.4%, the overall survival rate since HCC was 73.6% at 5 years. The overall survival rates since SVR were 98.7% and 93.6% at 5 and 10 years, respectively. Progression of HCC was the most frequent all-cause mortality, but none of the patients died of liver decompensation. Male sex and Fibrosis-4 index of ≥3.0 after SVR were significant and independent predictors of mortality.
Patients with HCV remain at risk of HCC for >10 years after achieving SVR, and HCC is the most common cause of mortality. We recommend long-term surveillance of cirrhotic patients with HCV, even after achieving SVR.
抗病毒治疗获得持续病毒学应答(SVR)对丙型肝炎病毒(HCV)感染的肝硬化患者肝脏并发症风险的长期影响,如食管静脉曲张(EV)加重、肝细胞癌(HCC)、恶性淋巴瘤以及肝脏相关死亡和全因死亡,目前尚不完全清楚。
在457例无HCC病史的HCV相关Child-Pugh A级肝硬化患者的长期随访中评估这些风险。
EV加重的5年和10年累积发生率分别为2.0%和3.1%。多变量分析确定EV的存在、基线血小板减少和酒精摄入是SVR前后EV加重的重要独立预测因素。HCC的5年和10年累积发生率分别为6.8%和10.2%。男性和EV的存在是SVR前后HCC的重要独立决定因素。虽然HCC的5年累积复发率为49.4%,但自HCC发生后5年的总生存率为73.6%。自SVR后的5年和10年总生存率分别为98.7%和93.6%。HCC进展是最常见的全因死亡原因,但没有患者死于肝失代偿。男性和SVR后Fibrosis-4指数≥3.0是死亡率的重要独立预测因素。
HCV患者在实现SVR后10多年仍有HCC风险,且HCC是最常见的死亡原因。我们建议对HCV肝硬化患者进行长期监测,即使在实现SVR后。