Sustained Virological Response in Special Populations with Chronic Hepatitis C Using Interferon-Free Treatments: A Systematic Review and Meta-analysis of Observational Cohort Studies

Clin Drug Investig. 2018 May;38(5):389-400. doi: 10.1007/s40261-018-0624-6.

Abstract

Background and objectives: Hepatitis C treatment has changed considerably in recent years, and many interferon (IFN)-free therapies are now available. Considering the high rates of sustained virological response (SVR) presented by clinical trials for these treatments, high rates of effectiveness are also expected in real-world clinical practice. Hence, this study aimed to conduct a systematic review and meta-analysis of observational cohort studies to evaluate the clinical effectiveness and safety of IFN-free therapies for hepatitis C.

Methods: The search was performed in four electronic databases and included cohort studies that evaluated IFN-free schemes and provided data on SVR at 12 weeks after the end of treatment (SVR12) as the primary outcome. Overall and subgroup meta-analyses of patients' clinical conditions (e.g. co-infection with human immunodeficiency virus (HIV), cirrhosis, liver transplant, specific genotypes, and other conditions) were performed.

Results: Sixty-eight studies encompassing a total of 24,151 patients were included for quantitative and qualitative analyses, evaluating six treatments: sofosbuvir with ledipasvir, daclatasvir, or simeprevir; daclatasvir with asunaprevir; paritaprevir/ritonavir in combination with ombitasvir and dasabuvir; and sofosbuvir with ribavirin. The overall analysis showed SVR rates of 88-96% for all treatments except sofosbuvir combined with ribavirin, which had SVR rates of approximately 80%. The results of subgroup analyses showed that the genotype 3 virus appears to be the most difficult to treat.

Conclusion: In order to choose the best treatment option, it is necessary to consider the patients' conditions and characteristics. In conclusion, the use of IFN-free therapies meets the high expectations created by clinical trials, including patients in special clinical conditions.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • 2-Naphthylamine
  • Anilides / administration & dosage
  • Antiviral Agents / administration & dosage*
  • Benzimidazoles / administration & dosage
  • Carbamates / administration & dosage
  • Cohort Studies
  • Cyclopropanes
  • Drug Therapy, Combination
  • Fluorenes / administration & dosage
  • Hepacivirus / drug effects
  • Hepacivirus / physiology
  • Hepatitis C, Chronic / diagnosis
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / epidemiology*
  • Humans
  • Interferons* / administration & dosage
  • Lactams, Macrocyclic
  • Macrocyclic Compounds / administration & dosage
  • Male
  • Middle Aged
  • Proline / analogs & derivatives
  • Ribavirin / administration & dosage
  • Ritonavir / administration & dosage
  • Simeprevir / administration & dosage
  • Sofosbuvir / administration & dosage
  • Sulfonamides / administration & dosage
  • Sustained Virologic Response*
  • Treatment Outcome
  • Uracil / administration & dosage
  • Uracil / analogs & derivatives
  • Valine

Substances

  • Anilides
  • Antiviral Agents
  • Benzimidazoles
  • Carbamates
  • Cyclopropanes
  • Fluorenes
  • Lactams, Macrocyclic
  • Macrocyclic Compounds
  • Sulfonamides
  • ledipasvir
  • ombitasvir
  • Ribavirin
  • Uracil
  • Interferons
  • Proline
  • Simeprevir
  • 2-Naphthylamine
  • dasabuvir
  • Valine
  • Ritonavir
  • paritaprevir
  • Sofosbuvir