首页> 外文期刊>Gut and Liver >Daclatasvir Plus Asunaprevir for the Treatment of Patients with Hepatitis C Virus Genotype 1b Infection: Real-World Efficacy, Changes in Liver Stiffness and Fibrosis Markers, and Safety
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Daclatasvir Plus Asunaprevir for the Treatment of Patients with Hepatitis C Virus Genotype 1b Infection: Real-World Efficacy, Changes in Liver Stiffness and Fibrosis Markers, and Safety

机译:达克他韦加Asunaprevir用于治疗丙型肝炎病毒基因型1b感染的患者:实际疗效,肝硬度和纤维化标志物变化以及安全性

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Background/Aims The treatment with daclatasvir plus asunaprevir (DCV+ASV) is associated with potent antiviral effects in patients with genotype 1b hepatitis C virus (HCV) infection. We investigated the real-world efficacy, changes in liver stiffness and noninvasive fibrosis markers, and the safety of DCV+ASV treatment in Korean patients. Methods In total, 363 patients with chronic hepatitis C were treated with DCV+ASV between August 2015 and January 2017. Finally, we analyzed the data of 270 patients who were monitored for at least 12 weeks after the end of treatment. Results The mean age was 60.7 years, and females predominated (60.4%). Most patients (64.8%) were treatment-na?ve, and 56 patients (20.7%) had cirrhosis. Two hundred fifty-seven (95.2%) and 251 (93.0%) patients achieved end-of-treatment responses and sustained virological responses at 12 weeks posttreatment (SVR12), respectively. The SVR12 rates were higher in patients who were <65 years of age, males, without cirrhosis and had lower HCV RNA levels. All LS values and fibrosis-4 and aspartate aminotransferase-to-platelet ratio index values declined from baseline to the time of assessment of SVR12. Conclusions The DCV+ASV therapy resulted in a high SVR12 and improved liver fibrosis; the treatment was well tolerated in patients with genotype 1b HCV infections.
机译:背景/目的达卡他韦+ Asunaprevir(DCV + ASV)的治疗与基因1b型丙型肝炎病毒(HCV)感染患者的抗病毒作用强相关。我们调查了韩国患者的实际疗效,肝硬度和非侵入性纤维化标志物的变化以及DCV + ASV治疗的安全性。方法在2015年8月至2017年1月期间,共对363例慢性丙型肝炎患者进行了DCV + ASV治疗。最后,我们分析了治疗结束后至少12周接受监测的270例患者的数据。结果平均年龄为60.7岁,女性占主导地位(60.4%)。多数患者(64.8%)未进行过治疗,有56例患者(20.7%)患有肝硬化。在治疗后12周(SVR12),有257例(95.2%)和251例(93.0%)患者分别达到治疗结束反应和持续的病毒学应答。小于65岁的男性,无肝硬化且HCV RNA水平较低的患者中SVR12的发生率较高。从基线到评估SVR12时,所有LS值,纤维化4和天冬氨酸转氨酶与血小板之比的指数值均下降。结论DCV + ASV疗法可导致较高的SVR12并改善肝纤维化。基因1b型HCV感染的患者对该治疗的耐受性良好。

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