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
Hye Won Lee,
Se Rim Oh,
Dong Yun Kim,
Yechan Jeong,
Seungtaek Kim,
Beom Kyung Kim,
Seung Up Kim,
Do Young Kim,
Sang Hoon Ahn,
Kwang-Hyub Han,
Jun Yong Park
Affiliations
Hye Won Lee
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Se Rim Oh
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Dong Yun Kim
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Yechan Jeong
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Seungtaek Kim
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Beom Kyung Kim
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Seung Up Kim
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Do Young Kim
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Sang Hoon Ahn
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Kwang-Hyub Han
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Jun Yong Park
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Background/AimsThe 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-naïve, 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.Conclusion : sThe DCV+ASV therapy resulted in a high SVR12 and improved liver fibrosis; the treatment was well tolerated in patients with genotype 1b HCV infections.