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Real-world efficacy and safety of Ledipasvir + Sofosbuvir and Om-bitasvir/Paritaprevir/Ritonavir ± Dasabuvir combination therapies for chronic hepatitis C: A Turkish experience
Author(s) -
Bülent Değertekın,
Mehmet Demir,
Ulus Salih Akarca,
Haluk Tarık Kani,
Enver Üçbilek,
Emre Yıldırım,
Fatih Güzelbulut,
Ayhan Balkan,
Sezgin Vatansever,
Nilay Danış,
Melek Demircan,
Aliye Soylu,
Serkan Yaraş,
Aysun Kartal,
Ayşe Kefeli,
Feyza Gündüz,
Kendal Yalçın,
Elife Erarslan,
Murat Aladağ,
Murat Harputluoğlu,
Ayşegül Özakyol,
Tuncer Temel,
Mesut Akarsu,
Hale Sümer,
Mete Akın,
Bülent Albayrak,
İlker Şen,
Hüseyin Alkım,
Ahmet UYANIKOĞLU,
Kader İrak,
Sinem Öztaşkın,
Çağrı Burak Uğurlu,
Şevkican Güneş,
Selım Gürel,
Kenan Nuriyev,
İsmail İncı̇,
Sabite Kaçar,
Dinc Dinçer,
Levent Doğanay,
Hüseyin Savaş Göktürk,
Ali Mert,
Arif Coşar,
Hakan Dursun,
Roni Atalay,
Sabiye Akbulut,
Yasemin Balkan,
Hayrettin Koklu,
Cem Şimşek,
Osman Özdoğan,
Mehmet Çoban
Publication year - 2021
Publication title -
the turkish journal of gastroenterology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.404
H-Index - 28
eISSN - 2148-5607
pISSN - 1300-4948
DOI - 10.5152/tjg.2020.20696
Subject(s) - ombitasvir , medicine , dasabuvir , sofosbuvir , paritaprevir , ledipasvir , simeprevir , ritonavir , ribavirin , gastroenterology , population , hepatitis c , hepatitis c virus , virology , viral load , virus , environmental health , antiretroviral therapy
BACKGROUND/AIMSThis 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 METHODSA 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.RESULTSSVR12 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%).CONCLUSIONLDV/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.

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