Danilau Dzmitry, Malich Nadzeya, Litvinchuk Dzmitry, Karpov Igor
Belarusian State Medical University, Belarus.
Clin Exp Hepatol. 2017 Sep;3(3):164-168. doi: 10.5114/ceh.2017.70281. Epub 2017 Sep 25.
Aim of the study is to evaluate real-world efficacy of the ombitasvir/ paritaprevir/ ritonavir + dasabuvir ± ribavirin for treatment of chronic hepatitis C 1 genotype.
The study included 27 patients according to inclusion criteria. Main laboratory studies were performed in all patients at the baseline and during the treatment.
Efficacy of the antiviral therapy was assessed by measuring the SVR12 and the SVR24 along with measuring of viral load during the treatment. The SVR12 and SVR24 rate was 100% (27/27).
The results of the treatment were comparable to the results of pivotal, large-scale, randomized clinical trials. There were no serious adverse events during the treatment.
本研究的目的是评估ombitasvir/ paritaprevir/ ritonavir + dasabuvir ± 利巴韦林治疗1型慢性丙型肝炎的真实疗效。
根据纳入标准,该研究纳入了27例患者。在基线期和治疗期间对所有患者进行了主要实验室检查。
通过测量治疗期间的SVR12和SVR24以及病毒载量来评估抗病毒治疗的疗效。SVR12和SVR24率为100%(27/27)。
治疗结果与关键的大规模随机临床试验结果相当。治疗期间未发生严重不良事件。