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首页> 外文期刊>Antiviral therapy >Clinical and virological response to entecavir in HBV-related chronic hepatitis or cirrhosis: Data from the clinical practice in a single-centre cohort
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Clinical and virological response to entecavir in HBV-related chronic hepatitis or cirrhosis: Data from the clinical practice in a single-centre cohort

机译:恩替卡韦在HBV相关慢性肝炎或肝硬化中的临床和病毒学应答:来自单中心队列临床实践的数据

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Background: Limited data are available on entecavir in Caucasian patients with HBV cirrhosis or chronic hepatitis B who are treated in the clinical practice. The aim was to evaluate the eficacy of entecavir in an Italian cohort of unselected patients with different stages of liver ibrosis, comparing the virological and clinical results obtained between patients with and without liver cirrhosis. Methods: Eficacy and safety of entecavir were retrospectively evaluated in 100 patients recruited in the Gastro- Hepatology Unit, San Giovanni Battista Hospital (Turin, Italy). A pharmacokinetic analysis was performed in 34 participants to assess whether cirrhosis may affect entecavir metabolism. Participants were followed-up for a median (range) duration of 21 months (2-108). Results: Rates of virological response (negative viraemia by PCR for ??2 consecutive determinations) after 12, 24 and 36 months were 91.7%, 97.5% and 93.7%, respectively. In the 84 patients who were treated for ??12 months, presence of cirrhosis (OR 1.730, 95% CI 1.082, 2.766; P=0.022) and absence of hepatitis B e antigen (OR 0.479, 95% CI 0.273, 0.842; P=0.011) were independent predictors of earlier clearance of serum HBV DNA. There were no differences between the serum concentrations in the steady-state level of entecavir between patients with or without cirrhosis. No signiicant differences were detected between the average area under the curve in the means of the two groups (P=0.55). Conclusions: Entecavir represents an excellent therapy in patients with HBV-related liver disease and particularly with cirrhosis where it showed a good proile of tolerability, higher eficacy and an earlier virological response. ? 2013 International Medical Press.
机译:背景:恩替卡韦在临床实践中接受治疗的白种人HBV肝硬化或慢性乙型肝炎患者的可用数据有限。目的是评估恩替卡韦在意大利未选择的具有不同肝纤维化阶段的患者队列中的疗效,比较有无肝硬化的患者的病毒学和临床结果。方法:回顾性评估了San Giovanni Battista医院(意大利都灵)胃肠病肝病科招募的100名患者的恩替卡韦的疗效和安全性。在34位参与者中进行了药代动力学分析,以评估肝硬化是否会影响恩替卡韦的代谢。对参与者进行了为期21个月(2-108)的中位(范围)随访。结果:12、24和36个月后的病毒学应答率(通过PCR连续2次测定阴性病毒血症)分别为91.7%,97.5%和93.7%。在治疗了12个月的84例患者中,存在肝硬化(OR 1.730,95%CI 1.082,2.766; P = 0.022)和缺乏乙型肝炎e抗原(OR 0.479,95%CI 0.273,0.842; P = 0.011)是血清HBV DNA早期清除的独立预测因子。在有或没有肝硬化的患者之间,恩替卡韦稳态水平的血清浓度之间没有差异。两组平均值的曲线下平均面积之间未检测到显着差异(P = 0.55)。结论:恩替卡韦是治疗HBV相关性肝病,尤其是肝硬化患者的一种极好的疗法,其表现出良好的耐受性,更高的疗效和更早的病毒学应答。 ? 2013国际医学出版社。

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