2016
Daclatasvir plus sofosbuvir, with or without ribavirin, achieved high sustained virological response rates in patients with HCV infection and advanced liver disease in a real-world cohort
Abstract: ObjectiveWe assessed the effectiveness and safety of daclatasvir (DCV) plus sofosbuvir (SOF), with or without ribavirin (RBV), in a large real-world cohort, including patients with advanced liver disease.DesignAdults with chronic HCV infection at high risk of decompensation or death within 12 months and with no available treatment options were treated in a European compassionate use programme. The recommended regimen was DCV 60 mg plus SOF 400 mg for 24 weeks; RBV addition or shorter duration was allowed at ph…
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Cited by 199 publications
(169 citation statements)
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“…The highest SVR (96%) was witnessed with group D who took sofosbuvir plus daclatasvir; this was rather close to that achieved in a number of lab trials, for example, in phase IIA of LONESTAR open-label trial where the SVR was approximately 98%, 92%, and 89% for of genotype 1, 2, and 3, respectively (Cholongitas et al, 2014and Sulkowski et al in 2014). It was also in agreement with a study done by Welzel et al [20], where SVR12 was achieved by 91% of patients. In contrast to Fontaine et al in 2015, cirrhotic patients receiving SOF + DCV + RBF and sofosbuvir and simprevir achieved a 100% SVR thus was considered a good therapeutic option.…”
Section: Discussionsupporting
confidence: 93%
“…The highest SVR (96%) was witnessed with group D who took sofosbuvir plus daclatasvir; this was rather close to that achieved in a number of lab trials, for example, in phase IIA of LONESTAR open-label trial where the SVR was approximately 98%, 92%, and 89% for of genotype 1, 2, and 3, respectively (Cholongitas et al, 2014and Sulkowski et al in 2014). It was also in agreement with a study done by Welzel et al [20], where SVR12 was achieved by 91% of patients. In contrast to Fontaine et al in 2015, cirrhotic patients receiving SOF + DCV + RBF and sofosbuvir and simprevir achieved a 100% SVR thus was considered a good therapeutic option.…”
Section: Discussionsupporting
confidence: 93%
“…Similarly, our results were in line with the research conducted by Welzel et al 12 Their study assessed the efficacy of daclatasvir and sofosbuvir across all genotypes. They found that HCV RNA was undetectable in 73% of cases at week 4 (Rapid Virological Response), while the End-of-Treatment Response (ETR) was 92%, and 99% of participants achieved SVR24.…”
Section: Discussionsupporting
confidence: 93%
“…Belperio et al 26 reported SVR12 rate in GT2 (94.5% without RBV and 88.1% with RBV) and GT3 (90.8% without RBV and 88.1% with RBV). In comparison to our response rate, similar findings are reported in other studies 22,27‐30 . These results supported that the chance of achieving a cure was higher with DCV + SOF then the DCV + SOF + RBV.…”
Section: Discussionsupporting
confidence: 93%
