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Sofosbuvir based treatment of chronic hepatitis C genotype 3 infections-A Scandinavian real-life study

Artikel i vetenskaplig tidskrift
Författare O. Dalgard
O. Weiland
G. Noraberg
L. Karlsen
L. Heggelund
M. Farkkila
U. Balslev
E. Belard
A. Ovrehus
M. S. Kjaer
H. Krarup
B. T. Roge
S. Hallager
L. G. Madsen
A. L. Laursen
Martin Lagging
N. Weis
Publicerad i Plos One
Volym 12
Nummer/häfte 7
ISSN 1932-6203
Publiceringsår 2017
Publicerad vid Institutionen för biomedicin
Språk en
Länkar dx.doi.org/10.1371/journal.pone.017...
Ämnesord ADVANCED LIVER-DISEASE, DECOMPENSATED CIRRHOSIS, PHASE-III, HCV, VIRUS, DACLATASVIR, RIBAVIRIN, EPIDEMIOLOGY, VELPATASVIR, LEDIPASVIR, Multidisciplinary Sciences
Ämneskategorier Virologi

Sammanfattning

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-a) + 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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