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Direct-acting antiviral agents in the treatment of chronic Hepatitis C – “Real-life” experience from an academic centre and two specialized clinical practices

机译:直接作用抗病毒剂治疗慢性丙型肝炎 - “现实生活”经验,学术中心和两个专业的临床实践

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The introduction of the new direct antiviral agents has revolutionized the therapy of chronic hepatitis C. Today we are able to cure the vast majority of our patients with an 8- to 12-week therapy course of an antiviral combination therapy with an excellent safety profile. Real-life data are very important to further develop our experience with the new therapeutics and help us to improve the care of our patients in our everyday clinical practice.In our study, we present the retrospective analysis of a representative German cohort of 344 patients with chronic hepatitis C treated with the new direct antiviral agents. The patients were recruited in an academic center of southern Germany (University Clinic of Ulm, Clinic of Internal Medicine I) and in 2 highly specialized clinical practices in the city center and the near region of Ulm. Within this in-detail characterized study cohort, we analyzed the efficacy and safety of antiviral therapy under real-life conditions.In 322 patients, we could document SVR12 data and found an excellent overall SVR12 rate of 97.8 % across all genotypes. In more detail, we could show comparable SVR12 results of 99 % and 99.2 % in patients with the hepatitis C virus subtypes 1a and 1b of and an excellent SVR12 rate of 93.1 % in genotype 3 patients without liver cirrhosis. Nevertheless, SVR12 rates tend to be lower in patients with the presence of liver cirrhosis, especially in genotype 3 patients with the lowest SVR12 rate in the whole study group of only 80 %. In general, there were no major safety issues except of 1 patient treated with a protease-inhibitor-based regimen who developed a generalized skin reaction and needed hospitalization and premature end of antiviral therapy.In summary, our analysis of this well characterized representative cohort of 344 patients adds more information in the field of real-life experience with the new antiviral therapeutics and could therefore contribute to improve the care of our patients. Together with the existing real-life data, we now can proceed in achieving the aim of viral eradication of hepatitis C virus within our population.
机译:新的直接抗病毒药物的引入已经彻底改变了慢性丙型肝炎的治疗。今天我们能够治愈绝大多数患者8至12周的抗病毒联合治疗的治疗过程,具有出色的安全性。现实生活数据对于进一步发展我们的新治疗方法非常重要,并帮助我们在日常临床实践中改善患者的照顾。我们的研究中,我们提出了对德国患者的代表德国队列的回顾性分析用新的直接抗病毒药治疗慢性丙型肝炎。患者被招募在德国南部的学术中心(ULM大学诊所,内科诊所I)和市中心的2个高度专业的临床实践和乌尔姆附近的地区。在这种详细的表征研究队列中,我们分析了抗病毒治疗在现实生活条件下的疗效和安全性。322例患者,我们可以记录SVR12数据,发现所有基因型的优异的总体SVR12率为97.8%。更详细地,我们可以呈现出可比的SVR12在丙型肝炎病毒亚型1A和1B患者中的99%和99.2%的结果,并且在没有肝硬化的基因型3患者中的优异SVR12率为93.1%。然而,肝硬化存在的患者中,SVR12速率往往会降低,特别是在整个研究组中最低SVR12率的基因型3患者中仅为80%。一般而言,除了用基于蛋白酶抑制剂的方案治疗的1例患者没有任何主要的安全问题,他们开发出广泛的皮肤反应并需要住院治疗和抗病患者过早的终止。在摘要中,我们对这一特征的代表性队列的分析344名患者在新的抗病毒治疗方法中增加了现实生活经验领域的更多信息,因此可以有助于改善患者的照顾。我们与现有的现实生活数据一起,我们现在可以进行在人口中实现病毒根除丙型肝炎病毒的目的。

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