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Sustained virologic response to direct-acting antiviral agents predicts better outcomes in hepatitis C virus-infected patients: A retrospective study

机译:对直接作用抗病毒药物的持续病毒学反应预测丙型肝炎病毒感染患者的更好的结果:回顾性研究

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BACKGROUND:Direct-acting antiviral agents (DAAs) are extremely effective in eradicating hepatitis C virus (HCV) in chronically infected patients. However, the protective role of the sustained virologic response (SVR) achieved by second- and third-generation DAAs against the onset of hepatocellular carcinoma (HCC) and mortality is less well established.AIM:To examine the occurrence of HCC or death from any cause in a retrospective-prospective study of patients treated with DAAs.METHODS:Patients were enrolled from a tertiary academic hospital center for liver disease management that collects subject data mainly from northeastern Italy. The study was conducted in 380 patients (age: 60 ± 13 years, 224 males, 32% with cirrhosis) treated with DAAs with or without SVR (95/5%), with a median follow up of 58 wk (interquartile range: 38-117). The baseline anthropometric features, HCV viral load, severity of liver disease, presence of extra-hepatic complications, coinfection with HIV and/or HBV, alcohol consumption, previous interferon use, alpha-fetoprotein levels, and renal function were considered to be confounders.RESULTS:The incidence rate of HCC in patients with and without SVR was 1.3 and 59 per 100 person-years, respectively (incidence rate ratio: 44, 95%CI: 15-136, P 0.001). Considering the combined endpoint of HCC or death from any cause, the hazard ratio (HR) for the SVR patients was 0.070 (95%CI: 0.025-0.194, P 0.001). Other independent predictors of HCC or death were low HCV viremia (HR: 0.808, P = 0.030), low platelet count (HR: 0.910, P = 0.041), and presence of mixed cryoglobulinemia (HR: 3.460, P = 0.044). Considering SVR in a multi-state model, the independent predictors of SVR achievement were absence of cirrhosis (HR: 0.521, P 0.001) and high platelet count (HR: 1.019, P = 0.026). Mixed cryoglobulinemia predicted the combined endpoint in patients with and without SVR (HR: 5.982, P = 0.028 and HR: 5.633, P = 0.047, respectively).CONCLUSION:DAA treatment is effective in inducing SVR and protecting against HCC or death. A residual risk of HCC persists in patients with advanced liver disease or with complications, such as mixed cryoglobulinemia or renal failure.?The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
机译:背景:直接作用抗病毒剂(DAAs)在慢性感染患者中消除丙型肝炎病毒(HCV)非常有效。然而,通过第二代和第三代DAAs对肝细胞癌(HCC)和死亡率发作来实现的持续的病毒性反应(SVR)的保护作用较小,成立了很少.aum:检查任何人的HCC或死亡对DAAS.Methods治疗的患者的回顾性预期研究原因:患者从高等教育疾病管理中心注册了肝病管理,主要来自意大利东北部的主题数据。该研究在380名患者(年龄:60±13岁,224名雄性,32%,肝硬化)进行,用DAAS或不含SVR(95/5%),中位于58周(四分位数范围:38 -117)。基线人类测量特征,HCV病毒载荷,肝病的严重程度,肝脏并发症的存在,与艾滋病毒和/或HBV的繁殖,醇消耗,先前的干扰素使用,α-胎蛋白水平和肾功能被认为是混杂的。结果:HCC患者患者和不含SVR的患者的发病率分别为每100人的1.3和59人(发病率比率:44,95%CI:15-136,P <0.001)。考虑到任何原因的HCC或死亡的组合终点,SVR患者的危险比(HR)为0.070(95%CI:0.025-0.194,P <0.001)。 HCC或死亡的其他独立预测因子是低HCV病毒血症(HR:0.808,P = 0.030),低血小板计数(HR:0.910,P = 0.041),以及混合冷冻蛋白血症的存在(HR:3.460,P = 0.044)。考虑到多状态模型中的SVR,SVR成就的独立预测因子缺乏肝硬化(HR:0.521,P <0.001)和高血小板计数(HR:1.019,P = 0.026)。混合的干酪蛋白血症预测患者的组合终点(HR:5.982,P = 0.028和HR:5.633,P = 0.047)。结论:DAA治疗可有效诱导SVR并防止HCC或死亡。 HCC的残余风险持续存在于高级肝病或并发症的患者,如混合的干酪肿血症或肾衰竭。作者2019年。由Baishideng Publishing Group Inc.出版的所有权利保留。

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