Prevalence of relevant NS5A resistance-associated substitutions to elbasvir in genotype 1a hepatitis C virus patients in Spain

Enferm Infecc Microbiol Clin (Engl Ed). 2018 May;36(5):262-267. doi: 10.1016/j.eimc.2017.03.008. Epub 2017 May 15.
[Article in English, Spanish]

Abstract

Resistance-associated substitutions (RASs) to the new HCV NS5A inhibitor elbasvir may limit its efficacy and lead to virological failure in HCV-GT1a-infected patients. There are no data outside clinical trials evaluating their prevalence and impact in grazoprevir/elbasvir in GT1a-infected patients in Spain. A multicentre cross-sectional study of 632 initial patients was conducted. In 13 of these patients, the sample could not be amplified or a consensus sequence by Sanger sequencing could not be performed. Ultimately, 617 HCV-G1a-infected individuals treated at 84 Spanish hospitals from the 17 autonomous communities plus the 2 autonomous cities of Spain were analysed. HCV population sequencing was used to identify RAS to elbasvir and the mutational pattern and drug sensitivity were confirmed by geno2pheno[HCV]. Viruses bearing RASs to elbasvir were present in 6.2% of HCV-G1a infected patients. The most common RASs were the Y93C/H/N and Q30E/H/R (2.4% and 2.3%, respectively). Only 3.4% of the identified RASs to elbasvir conferred reduced susceptibility to elbasvir by geno2pheno[HCV], which exclusively identified the positions Q30H/R (n=7) and Y93C/H/N (n=8) as single mutations and Q30H+Y93H (n=4) and Q30R+Y93H (n=2) as double mutations as the major RASs to elbasvir. A lower prevalence of RASs to elbasvir was observed in our HCV-G1a Spanish cohort than reported previously in clinical trials evaluating patients from the USA. This information may be essential to guide the implementation of grazoprevir/elbasvir in Spain and to manage G1a-infected patients.

Keywords: Antivirales de acción directa; Coinfección virus de la hepatitis C / virus de la inmunodeficiencia humana; Direct-acting antiviral agents; Elbasvir implementation; Genotype substitution; Hepatitis C virus / human immunodeficiency virus-coinfection; Implementación elbasvir; Prevalence; Prevalencia; Sustitución genotípica.

Publication types

  • Multicenter Study

MeSH terms

  • Amino Acid Substitution*
  • Benzofurans / therapeutic use*
  • Cross-Sectional Studies
  • Drug Resistance, Viral*
  • Female
  • Genotype
  • Hepacivirus / drug effects
  • Hepacivirus / genetics*
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / virology*
  • Humans
  • Imidazoles / therapeutic use*
  • Male
  • Middle Aged
  • Spain
  • Viral Nonstructural Proteins / genetics*

Substances

  • Benzofurans
  • Imidazoles
  • Viral Nonstructural Proteins
  • elbasvir
  • NS-5 protein, hepatitis C virus