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Sofosbuvir based treatment of chronic hepatitis C genotype 3 infections-A Scandinavian real-life study
Olav Dalgard1,2, Ola Weiland3, Geir Noraberg4
1Akershus University Hospital, Lørenskog, Norway.
Insights
Sofosbuvir-based regimens achieve over 90% sustained virological response in patients with advanced liver disease due to hepatitis C virus genotype 3 infection. This real-world Scandinavian study confirms high efficacy for challenging HCV cases.
Area of Science:
- Hepatology
- Virology
- Clinical Medicine
Background:
- Hepatitis C virus (HCV) genotype 3 with advanced liver disease presents significant treatment challenges.
- Real-world data on sofosbuvir-based regimens for this population are crucial.
Purpose of the Study:
- To assess the effectiveness of sofosbuvir-based treatments for HCV genotype 3 in a Scandinavian real-life setting.
- To evaluate sustained virological response (SVR12) rates in patients with advanced liver disease.
Main Methods:
- Retrospective analysis of 316 patients with HCV genotype 3 across 16 Scandinavian centers.
- Patients received various sofosbuvir-containing regimens (SOF+RBV, SOF+DCV, SOF+peg-IFN-α, SOF/LDV) for 12-24 weeks.
- Fibrosis assessed by biopsy or elastography; SVR12 was the primary endpoint.
Main Results:
- An overall SVR12 rate of 91% (284/311) was achieved in the modified intention-to-treat population.
- Treatment regimens showed similar efficacy, but lower rates were observed in men (p=0.042) and patients with decompensated liver disease (p=0.004).
- The majority of patients had advanced liver disease, including cirrhosis (compensated and decompensated).
Conclusions:
- Sofosbuvir-based treatment demonstrates high efficacy (over 90% SVR) in real-world settings for HCV genotype 3 with advanced liver disease.
- These findings support the use of sofosbuvir regimens for difficult-to-treat HCV cases.
- Further research may explore factors influencing treatment outcomes in specific patient subgroups.
Background And Aims:
Chronic hepatitis C virus (HCV) genotype 3 infection with advanced liver disease has emerged as the most challenging to treat. We retrospectively assessed the treatment outcome of sofosbuvir (SOF) based regimes for treatment of HCV genotype 3 infections in a real life setting in Scandinavia.
Methods:
Consecutive patients with chronic HCV genotype 3 infection were enrolled at 16 treatment centers in Denmark, Sweden, Norway and Finland. Patients who had received a SOF containing regimen were included. The fibrosis stage was evaluated by liver biopsy or transient liver elastography. The following treatments were given according availability and local guidelines: 1) SOF + ribavirin (RBV) for 24 weeks, 2) SOF + daclatasvir (DCV) +/-RBV for 12-24 weeks, 3) SOF + pegylated interferon alpha (peg-IFN-α) + RBV for 12 weeks or 4) SOF/ledipasvir (LDV) + RBV for 12-16 weeks. The primary endpoint was sustained virological response (SVR) assessed at week 12 (SVR12) after end of treatment.
Results:
We included 316 patients with a mean age of 55 years (range 24-79), 70% men, 49% treatment experienced, 58% with compensated cirrhosis and 12% with decompensated cirrhosis.In the modified intention to treat (mITT) population SVR12 was achieved in 284/311 (91%) patients. Among 26 treatment failures, five had non-response, 3 breakthrough and 18 relapse. Five patients were not included in the mITT population. Three patients died from reasons unrelated to treatment and two were lost to follow-up. The SVR12 rate was similar for all treatment regimens, but lower in men (p = 0.042), and in patients with decompensated liver disease (p = 0.004).
Conclusion:
We found that sofosbuvir based treatment in a real-life setting could offer SVR rates exceeding 90% in patients with HCV genotype 3 infection and advanced liver disease.
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