Original Articles

Vol. 37 No. 6 (2026): Turkish Journal of Gastroenterology

Efficacy and Safety of Direct-Acting Antivirals in Patients with Hepatitis C Infection: Nationwide Real-life Data from Türkiye

Main Article Content

Alper Gunduz
Nefise Çuvalcı Öztoprak
Nagehan Didem Sarı
Behice Kurtaran
Yusuf Önlen
Ebubekir Senates
Esra Zerdali
Hasan Karsen
Ayse Batırel
Rıdvan Kara Ali
Rahmet Güner
Tansu Yamazhan
Sukran Kose
Nurettin Erben
Nevin Ince
İftihar Köksal
Figen Sarıgül Yıldırım
Gulsen Yoruk
Suheyla Komur
Tayibe Bal
Sibel Kaya
Şaban Esen
Özgür Günal
Ilknur Esen Yıldız
Dilara Inan
Şener Barut
Mustafa Namıduru
Selma Tosun
Kamuran Türker
Alper Sener
Kenan Hızel
Nurcan Baykam
Fazilet Duygu
Esragül Akıncı
Güray Can
Ulku User
Hanefi Cem Gül
Ayhan Akbulut
Güven Çelebi
Mahmut Sünnetçioğlu
Oğuz Karabay
Hayat Kumbasar Karaosmanoğlu
Fatma Sırmatel
Fehmi Tabak

Abstract

Background/Aims: Chronic hepatitis C virus (HCV) infection constitutes a substantial healthcare concern in Türkiye. The clinical application of direct-acting antiviral medications (DAAs) has transformed its management. The goal is to assess the efficacy and safety of DAAs in the real-world setting in Turkish patients with chronic HCV.


Materials and Methods: Thirty-seven centers from Türkiye recorded 1807 patients to the database. Patients aged >18 years were enrolled to the study. Their demographics, clinical information, DAAs used, efficacy, and safety information were evaluated. Efficacy and safety results were reported for patients with 12-week post-treatment (SVR12) data.


Results: Among the patients, 919 (50.9%) were female with a mean of age 56 Å} 15 years (range:18-97 years) and 238 (13%) were cirrhotic. Liver biopsy was performed in 296 patients. Mean histologic activity index score was 7.68 and fibrosis score was 2.58. Baseline mean viral load was 4.11Å~106 copies/mL. Patients received the following treatments: Paritaprevir+Ritonavir+Ombitasvir+Dasabuvir (PrOD):706, Ledipasvir+Sofosbuvir:490, Sofosbuvir+Ribavirin:176, PrOD+Ribavirin:175, Ledipasvir+Sofosbuvir+Ribavirin:156, PrO+Ribavirin:32, and PrO:10. Response at the end of treatment was 99.2% (1454/1465) and SVR12 was 97.8% (1289/1318). The DAAs were generally well tolerated. Ten and 13 patients discontinued therapy because of drug-related and unrelated adverse side effects, respectively.


Conclusion: This real-world study demonstrated that DAA treatment for HCV is both safe and highly effective. In two-thirds of the patients, the hepatic inflammation is moderate to severe, and fibrosis is moderate to advanced in half of them. Patients’ characteristics suggest that HCV infection is often not diagnosed or treated until patients present with moderate-to-severe stage, indicating that diagnostic and therapeutic approaches should be used more effectively.


 


Cite this article as: Gunduz A, .ztoprak N., Sarı ND, et al. Efficacy and safety of direct-acting antivirals in patients with hepatitis  infection: nationwide real-life data from Türkiye. Turk J Gastroenterol. 2026;37(6):673-681.

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