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首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Long-term outcome of hepatocellular carcinoma occurrence, esophageal varices exacerbation, and mortality in hepatitis C virus-related liver cirrhosis after interferon-based therapy
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Long-term outcome of hepatocellular carcinoma occurrence, esophageal varices exacerbation, and mortality in hepatitis C virus-related liver cirrhosis after interferon-based therapy

机译:肝细胞癌发生的长期结果,食管变化加剧,干扰素治疗后丙型肝炎病毒相关肝硬化的死亡率和死亡率

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Aim 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. Methods 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. Results 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. Conclusion 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.
机译:瞄准持续的病毒性反应(SVR)对抗病毒疗法的长期影响对肝脏并发症的风险,例如食管静脉曲化(EV),肝细胞癌(HCC),恶性淋巴瘤和肝脏相关和整体死亡的抗病治疗丙型肝炎病毒(HCV) - 肝硬化患者患者尚未完全清楚。方法评估这些风险在长期跟进457例HCV相关的儿童-PUGH课程肝硬化患者中进行评估,没有HCC历史。结果各自的累积5-和10年的EV加剧率为2.0%和3.1%。多变量分析确定了基线的EVS,血小板减少症的存在。酒精摄入量作为SVR之前和之后的EV加剧的重要预测因子。累积5-和10年的HCC率分别为6.8%和10.2%。男性性别和EV的存在是SVR之前和之后HCC的重要决定因素。虽然累积5年的HCC复发率为49.4%,但由于HCC以来的整体存活率为5年以来为73.6%。 SVR以来的总存活率分别为98.7%和93.6%,分别为5和10年。 HCC的进展是最常见的全导致死亡率,但患有肝脏失代偿的患者都没有死亡。男性性和纤维化-4 SVR = 3.0索引的纤维化和纤维化-4指数是显着的和独立的死亡率预测因子。结论HCV患者持续存在HCC的风险> 10年后达到SVR,HCC是最常见的死亡原因。我们建议在达到SVR后,建议使用HCV的肝硬化患者长期监测。

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