Liver - Original Article

Vol. 31 No. 12 (2020): 2020.31.12-Turkish Journal of Gastroenterology

Real-world efficacy and safety of Ledipasvir + Sofosbuvir and Ombitasvir/Paritaprevir/Ritonavir ± Dasabuvir combination therapies for chronic hepatitis C: A Turkish experience

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Levent Doğanay
İlker Sen
Hüseyin Alkım
Ahmet Uyanıkoğlu 0
Kader Irak
Sinem Öztaşkın
Çağrı Burak Uğurlu
Şevkican Güneş
Selim Gürel
Kenan Nuriyev
İsmail İnci
Sabite Kaçar
Dinç Dinçer
Bülent Albayrak
Hüseyin Savaş Göktürk
Ali Mert
Arif Mansur Coşar
Hakan Dursun
Roni Atalay
Sabiye Akbulut
Yasemin Balkan 0
Hayrettin Koklu
Halis Şimşek
Osman Özdoğan
Mehmet Çoban
Aysun Kartal
Mehmet Demir
Ulus S. Akarca
Haluk Tarık Kani
Enver Üçbilek
Emre Yıldırım
Fatih Güzelbulut
Ayhan Balkan
Sezgin Vatansever
Nilay Danış
Melek Demircan
Aliye Soylu 0
Serkan Yaras
Bülent Değertekin
Ayşe Kefeli
Feyza Gündüz
Kendal Yalçın
Elife Erarslan
Murat Aladağ
Murat Harputluoğlu
Ayşegül Özakyol
Tuncer Temel
Mesut Akarsu
Hale Sümer
Mete Akın

Abstract

Background/Aims: This study aimed to evaluate the real-life efficacy and tolerability of direct-acting antiviral treatments for patients with chronic hepatitis C (CHC) with/without cirrhosis in the Turkish population.
Material and Methods: A total of 4,352 patients with CHC from 36 different institutions in Turkey were enrolled. They received ledipasvir (LDV) and sofosbuvir (SOF)±ribavirin (RBV) orombitasvir/paritaprevir/ritonavir±dasabuvir (PrOD)±RBV for 12 or 24 weeks. Sustained virologic response (SVR) rates, factors affecting SVR, safety profile, and hepatocellular cancer (HCC) occurrence were analyzed.
Results: SVR12 was achieved in 92.8% of the patients (4,040/4,352) according to intention-to-treat and in 98.3% of the patients (4,040/4,108) according to per-protocol analysis. The SVR12 rates were similar between the treatment regimens (97.2%–100%) and genotypes (95.6%–100%). Patients achieving SVR showed a significant decrease in the mean serum alanine transaminase (ALT) levels (50.90±54.60 U/L to 17.00±14.50 U/L) and model for end-stage liver disease (MELD) scores (7.51±4.54 to 7.32±3.40) (p<0.05). Of the patients, 2 were diagnosed with HCC during the treatment and 14 were diagnosed with HCC 37.0±16.0 weeks post-treatment. Higher initial MELD score (odds ratio [OR]: 1.92, 95% confidence interval [CI]: 1.22–2.38; p=0.023]), higher hepatitis C virus (HCV) RNA levels (OR: 1.44, 95% CI: 1.31–2.28; p=0.038), and higher serum ALT levels (OR: 1.38, 95% CI: 1.21–1.83; p=0.042) were associated with poor SVR12. The most common adverse events were fatigue (12.6%), pruritis (7.3%), increased serum ALT (4.7%) and bilirubin (3.8%) levels, and anemia (3.1%).
Conclusion: LDV/SOF or PrOD±RBV were effective and tolerable treatments for patients with CHC and with or without advanced liver disease before and after liver transplantation. Although HCV eradication improves the liver function, there is a risk of developing HCC.
Cite this article as: Değertekin B, Demir M, Akarca US, et al. Real-world efficacy and safety of Ledipasvir + Sofosbuvir and Om-bitasvir/Paritaprevir/Ritonavir ± Dasabuvir combination therapies for chronic hepatitis C: A Turkish experience. Turk J Gastroenterol 2020; 31(12): 883-93.

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