Real-world experience with Grazoprevir/Elbasvir in the treatment of previously "difficult to treat" patients infected with hepatitis C virus genotype 1 and 4

J Gastroenterol Hepatol. 2020 Jul;35(7):1238-1246. doi: 10.1111/jgh.14936. Epub 2020 Jan 16.

Abstract

Background and aim: Grazoprevir/elbasvir (GZR/EBR) was approved for the treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infected patients with or without compensated liver cirrhosis. The aim of this study was to assess GZR/EBR regimen in the real-world experience, particularly in previously "difficult-to-treat" patients with chronic kidney diseases, human immunodeficiency virus-coinfected, cirrhotics, and treatment-experienced.

Methods: The analysis included patients treated with GZR/EBR selected from 10 152 individuals from the EpiTer-2 database, large national real-world study evaluating antiviral treatment in 22 Polish hepatology centers between 2015 and 2018. Data were completed retrospectively and submitted online.

Results: A total of 1615 patients who started GZR/EBR therapy in 2017 and 2018 with a female predominance (54%) and median age of 54 years were analyzed. The majority were infected with GT1b (89%) and treatment naïve (81%). Liver cirrhosis was diagnosed in 19%, and 70% of patients had comorbidities, of which chronic renal disease was present in 7% and HIV-coinfection in 4%. Overall, a sustained virologic response (SVR) was achieved by 95% according to intent-to-treat (ITT) and 98% after exclusion of lost to follow up (modified ITT). No differences were found in cure rate between all included patients and subpopulations previously considered as difficult-to-treat. Majority of patients completed the treatment course as scheduled, adverse events were mostly mild and did not lead to therapy discontinuation.

Conclusions: GZR/EBR treatment carried-out in patients infected with HCV genotype 1 and 4 demonstrated good tolerability and an excellent SVR rate with no effectiveness reduction in so called difficult-to-treat populations.

Keywords: DAA; HCV; difficult-to-treat; grazoprevir/elbasvir; treatment.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Amides
  • Antiviral Agents / administration & dosage
  • Benzofurans / administration & dosage*
  • Carbamates
  • Comorbidity
  • Cyclopropanes
  • Data Analysis
  • Drug Therapy, Combination
  • Female
  • Genotype*
  • HIV Infections / epidemiology
  • Hepacivirus / genetics*
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / epidemiology
  • Hepatitis C, Chronic / virology*
  • Humans
  • Imidazoles / administration & dosage*
  • Liver Cirrhosis / epidemiology
  • Male
  • Middle Aged
  • Quinoxalines / administration & dosage*
  • Renal Insufficiency, Chronic / epidemiology
  • Retrospective Studies
  • Sex Factors
  • Sulfonamides
  • Sustained Virologic Response
  • Treatment Outcome
  • Young Adult

Substances

  • Amides
  • Antiviral Agents
  • Benzofurans
  • Carbamates
  • Cyclopropanes
  • Imidazoles
  • Quinoxalines
  • Sulfonamides
  • grazoprevir
  • elbasvir