The efficacy and tolerability of glecaprevir/pibrentasvir treatment in a real-world chronic hepatitis C patients cohort
dc.authorid | COSAR, Arif Mansur/0000-0002-4472-2895 | |
dc.authorid | Adanir, Haydar/0000-0003-1899-5846 | |
dc.contributor.author | Yaras, Serkan | |
dc.contributor.author | Demir, Mehmet | |
dc.contributor.author | Barutcu, Sezgin | |
dc.contributor.author | Yildirim, Abdullah Emre | |
dc.contributor.author | Gurel, Selim | |
dc.contributor.author | Ucbilek, Enver | |
dc.contributor.author | Kurtulmus, Ilkce Akgun | |
dc.date.accessioned | 2024-09-18T20:08:25Z | |
dc.date.available | 2024-09-18T20:08:25Z | |
dc.date.issued | 2023 | |
dc.department | Hatay Mustafa Kemal Üniversitesi | en_US |
dc.description.abstract | Background and Aim: The aims of the present study were to evaluate the real-life efficacy and tolerability of glecaprevir (GLE)/pibrentasvir (PIB) in the treatment of patients with chronic hepatitis C (CHC).Materials and Methods: Between May 2019 and May 2022, 686 patients with CHC, treated with GLE/PIB combination from 21 participating centers in Turkiye, were enrolled in the study.Results: All patients were Caucasian, and their median age was 56 years. At the start of GLE/PIB treatment, the median serum Hepatitis C virus RNA and serum alanine amino transaminase (ALT) levels were 6.74 log10 IU/mL and 47 U/L, respectively. Fifty-three percent of the patients were infected with genotype 1b, followed by genotype 3 (17%). Diabetes was the more common concomitant disease. The sustained virological response (SVR12) was 91.4% with intent-to-treat analysis and 98.5% with per protocol analysis. The SVR12 rates were statistically significant differences between the patients who were i.v. drug users and non-user (88.0% vs. 98.8%, p=0.025). From the baseline to SVR12, the serum ALT levels and Model for End-Stage Liver Disease score were significantly improved (p<0.001 and p=0.014, respectively). No severe adverse effect was observed.Conclusion: GLE/PIB is an effective and tolerable treatment in patients with CHC. | en_US |
dc.identifier.doi | 10.14744/hf.2023.2023.0001 | |
dc.identifier.endpage | 96 | en_US |
dc.identifier.issn | 1307-5888 | |
dc.identifier.issn | 2757-7392 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 37822314 | en_US |
dc.identifier.scopus | 2-s2.0-85172393527 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 92 | en_US |
dc.identifier.uri | https://doi.org/10.14744/hf.2023.2023.0001 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12483/8822 | |
dc.identifier.volume | 4 | en_US |
dc.identifier.wos | WOS:001078775900002 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Kare Publ | en_US |
dc.relation.ispartof | Hepatology Forum | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Chronic hepatitis C | en_US |
dc.subject | glecaprevir-pibrentasvir | en_US |
dc.subject | real-life experience | en_US |
dc.title | The efficacy and tolerability of glecaprevir/pibrentasvir treatment in a real-world chronic hepatitis C patients cohort | en_US |
dc.type | Article | en_US |
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