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

Dalgard, O. (författare)
Weiland, O. (författare)
Karolinska Institutet
Noraberg, G. (författare)
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Karlsen, L. (författare)
Heggelund, L. (författare)
Farkkila, M. (författare)
Balslev, U. (författare)
Belard, E. (författare)
Ovrehus, A. (författare)
Kjaer, M. S. (författare)
Krarup, H. (författare)
Roge, B. T. (författare)
Hallager, S. (författare)
Madsen, L. G. (författare)
Laursen, A. L. (författare)
Lagging, Martin, 1965 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin,Institute of Biomedicine
Weis, N. (författare)
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 (creator_code:org_t)
2017-07-13
2017
Engelska.
Ingår i: Plos One. - : Public Library of Science (PLoS). - 1932-6203. ; 12:7
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • 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.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)

Nyckelord

ADVANCED LIVER-DISEASE
DECOMPENSATED CIRRHOSIS
PHASE-III
HCV
VIRUS
DACLATASVIR
RIBAVIRIN
EPIDEMIOLOGY
VELPATASVIR
LEDIPASVIR
Multidisciplinary Sciences

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