Effectiveness of dasabuvir/ombitasvir/paritaprevir/ritonavir for hepatitis C virus in clinical practice: A population-based observational study

PLoS One. 2017 Jul 7;12(7):e0176858. doi: 10.1371/journal.pone.0176858. eCollection 2017.

Abstract

Background: Direct acting antivirals for hepatitis C virus have shown dramatic results in clinical trials. However, their effectiveness has yet to be demonstrated within observational cohorts which lack exclusion criteria found in randomized control trials.

Aim: To determine the effectiveness of dasabuvir/ombitasvir/paritaprevir/ritonavir in achieving sustained virological response.

Methods: Retrospective observational cohort study of all Clalit Health Services members with hepatitis C virus genotype 1 who were dispensed dasabuvir/ombitasvir/paritaprevir/ritonavir from January 1, 2015 to-November 31, 2015.

Results: There were 564 participants during the study period. The average age was 61.9 years, 52.0% were male, and 61.5% were born Eastern/Central Europe or Central Asia. The prevalence of diabetes was 31.7% and 70.3% were overweight/obese. Cirrhosis was present in 41.0% of participants, of whom 52.8% had stage 4 fibrosis. Of the cohort, 416 (74.8%) had follow-up viral load testing at 10 or more weeks after the end of treatment. We report a sustained virological response of 98.8% among those tested.

Conclusions: Treatment with dasabuvir/ombitasvir/paritaprevir/ritonavir demonstrated a near universal effectiveness in achieving a sustained virological response among HCV patients in a large cohort.

MeSH terms

  • 2-Naphthylamine
  • Aged
  • Anilides / administration & dosage
  • Carbamates / administration & dosage
  • Cyclopropanes
  • Drug Combinations*
  • Female
  • Genotype
  • Hepacivirus / drug effects*
  • Hepacivirus / pathogenicity
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / pathology
  • Hepatitis C, Chronic / virology
  • Humans
  • Lactams, Macrocyclic
  • Liver Cirrhosis / drug therapy*
  • Liver Cirrhosis / pathology
  • Liver Cirrhosis / virology
  • Macrocyclic Compounds / administration & dosage
  • Male
  • Middle Aged
  • Proline / analogs & derivatives
  • Ritonavir / administration & dosage
  • Sulfonamides / administration & dosage
  • Uracil / administration & dosage
  • Uracil / analogs & derivatives
  • Valine
  • Viral Load / drug effects

Substances

  • Anilides
  • Carbamates
  • Cyclopropanes
  • Drug Combinations
  • Lactams, Macrocyclic
  • Macrocyclic Compounds
  • Sulfonamides
  • ombitasvir
  • Uracil
  • Proline
  • 2-Naphthylamine
  • dasabuvir
  • Valine
  • Ritonavir
  • paritaprevir

Grants and funding

The authors received no specific funding for this work.