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

dc.contributor.authorKarasu, Zeki
dc.contributor.authorAyyıldız, Talat
dc.contributor.authorBalkan, Ayhan
dc.contributor.authorKani, Haluk Tarik
dc.contributor.authorIdilman, Ramazan
dc.contributor.authorKartal, Aysun Çalışkan
dc.contributor.authorSezgin, Orhan
dc.date.accessioned2026-10-09T21:21:00Z
dc.date.issued2020
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstractBackground/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) ombitasvir/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.
dc.identifier.doi10.5152/tjg.2020.20696
dc.identifier.endpage893
dc.identifier.issn1300-4948
dc.identifier.issn2148-5607
dc.identifier.issue12
dc.identifier.startpage883
dc.identifier.trdizinid453250
dc.identifier.urihttps://doi.org/10.5152/tjg.2020.20696
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/453250
dc.identifier.urihttps://hdl.handle.net/20.500.12794/1149
dc.identifier.volume31
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.relation.ispartofTurkish Journal of Gastroenterology
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_TR-Dizin_20260922
dc.subjectTıbbi Araştırmalar Deneysel
dc.subjectGastroenteroloji ve Hepatoloji
dc.titleReal-world efficacy and safety of Ledipasvir + Sofosbuvir andOmbitasvir/Paritaprevir/Ritonavir ± Dasabuvir combinationtherapies for chronic hepatitis C: A Turkish experience
dc.typeArticle

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