Uptake of tenofovir-based antiretroviral therapy among HIV-HBV-coinfected patients in the EuroSIDA study

Antivir Ther. 2018;23(5):405-413. doi: 10.3851/IMP3218.

Abstract

Background: According to guidelines all HIV-HBV-coinfected patients should receive tenofovir-based combination antiretroviral therapy (cART). We aimed to investigate uptake and outcomes of tenofovir-based cART among HIV-HBV patients in the EuroSIDA study.

Methods: All hepatitis B surface antigen (HBsAg)+ patients followed up after 1 March 2002 were included. Changes in the proportion taking tenofovir-based cART over time were described. Poisson regression was used to investigate the relationship between tenofovir use and clinical events.

Results: 953 HIV-HBV patients were included. Median age was 41 years and patients were predominantly male (85%), White (82%) and ART-experienced (88%). 697 and 256 were from Western and Eastern Europe, respectively. 55 started cART during follow-up, the proportion starting with CD4+ T-cell count <350 cells/mm3 decreased from 85% to 52% in the periods 2002-2006 to 2007-2015. Tenofovir use, among those taking cART, increased from 4% in 2002 to 73% in 2015. Compared to West, tenofovir use was lower in East in 2005 (7% versus 42%), and remained lower in 2015 (63% versus 76%). Among 602 patients taking tenofovir-based cART during follow-up, 155 (26%) discontinued tenofovir. 27 of all discontinuations were due to adverse effects. Only 14 started entecavir and/or adefovir after tenofovir discontinuation, whereas 10 started pegylated interferon. Tenofovir use was not significantly associated with lower risk of liver-related clinical events (n=51), adjusted incidence rate ratio (IRR) 0.64 (95% CI 0.35, 1.18) for comparing patients on tenofovir with those off tenofovir.

Conclusions: Although use of tenofovir-based cART among HIV-HBV patients has increased across Europe, a substantial proportion are still starting cART late and are receiving suboptimal HBV therapy.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / therapeutic use
  • Adult
  • Anti-Retroviral Agents / therapeutic use*
  • Antiretroviral Therapy, Highly Active
  • CD4 Lymphocyte Count
  • Coinfection
  • DNA, Viral / antagonists & inhibitors
  • DNA, Viral / biosynthesis
  • DNA, Viral / genetics
  • Drug Resistance, Viral / drug effects
  • Drug Utilization / statistics & numerical data*
  • Europe
  • Female
  • Guanine / analogs & derivatives
  • Guanine / therapeutic use
  • HIV / drug effects
  • HIV / genetics
  • HIV / metabolism
  • HIV Infections / drug therapy*
  • HIV Infections / virology
  • Hepatitis B Surface Antigens / blood
  • Hepatitis B virus / drug effects
  • Hepatitis B virus / genetics
  • Hepatitis B virus / metabolism
  • Hepatitis B, Chronic / drug therapy*
  • Hepatitis B, Chronic / virology
  • Humans
  • Interferon-alpha / therapeutic use
  • Lamivudine / therapeutic use
  • Male
  • Middle Aged
  • Organophosphonates / therapeutic use
  • Polyethylene Glycols / therapeutic use
  • Practice Guidelines as Topic
  • Prospective Studies
  • Recombinant Proteins / therapeutic use
  • Tenofovir / therapeutic use*

Substances

  • Anti-Retroviral Agents
  • DNA, Viral
  • Hepatitis B Surface Antigens
  • Interferon-alpha
  • Organophosphonates
  • Recombinant Proteins
  • Lamivudine
  • Polyethylene Glycols
  • entecavir
  • Guanine
  • adefovir
  • Tenofovir
  • Adenine
  • peginterferon alfa-2a