Prevalence of voriconazole-resistant invasive aspergillosis and its impact on mortality in haematology patients

J Antimicrob Chemother. 2019 Sep 1;74(9):2759-2766. doi: 10.1093/jac/dkz258.

Abstract

Background: Increasing resistance of Aspergillus fumigatus to triazoles in high-risk populations is a concern. Its impact on mortality is not well understood, but rates from 50% to 100% have been reported.

Objectives: To determine the prevalence of voriconazole-resistant A. fumigatus invasive aspergillosis (IA) and its associated mortality in a large multicentre cohort of haematology patients with culture-positive IA.

Methods: We performed a multicentre retrospective study, in which outcomes of culture-positive haematology patients with proven/probable IA were analysed. Patients were stratified based on the voriconazole susceptibility of their isolates (EUCAST broth microdilution test). Mycological and clinical data were compared, along with survival at 6 and 12 weeks.

Results: We identified 129 A. fumigatus culture-positive proven or probable IA cases; 103 were voriconazole susceptible (79.8%) and 26 were voriconazole resistant (20.2%). All but one resistant case harboured environment-associated resistance mutations in the cyp51A gene: TR34/L98H (13 cases) and TR46/Y121F/T289A (12 cases). Triazole monotherapy was started in 75.0% (97/129) of patients. Mortality at 6 and 12 weeks was higher in voriconazole-resistant cases in all patients (42.3% versus 28.2%, P = 0.20; and 57.7% versus 36.9%, P = 0.064) and in non-ICU patients (36.4% versus 21.6%, P = 0.16; and 54.4% versus 30.7%; P = 0.035), compared with susceptible ones. ICU patient mortality at 6 and 12 weeks was very high regardless of triazole susceptibility (75.0% versus 66.7%, P = 0.99; and 75.0% versus 73.3%, P = 0.99).

Conclusions: A very high prevalence of voriconazole resistance among culture-positive IA haematology patients was observed. The overall mortality at 12 weeks was significantly higher in non-ICU patients with voriconazole-resistant IA compared with voriconazole-susceptible IA.

Publication types

  • Multicenter Study

MeSH terms

  • Aged
  • Antifungal Agents / pharmacology*
  • Antifungal Agents / therapeutic use
  • Aspergillosis / drug therapy
  • Aspergillosis / epidemiology*
  • Aspergillosis / etiology*
  • Aspergillosis / mortality
  • Aspergillus fumigatus / drug effects
  • Aspergillus fumigatus / genetics
  • Cytochrome P-450 Enzyme System / genetics
  • Drug Resistance, Fungal*
  • Drug Therapy, Combination
  • Female
  • Fungal Proteins / genetics
  • Hematologic Neoplasms / complications*
  • Hematologic Neoplasms / epidemiology
  • Humans
  • Invasive Fungal Infections / drug therapy
  • Invasive Fungal Infections / epidemiology
  • Invasive Fungal Infections / etiology
  • Invasive Fungal Infections / mortality
  • Male
  • Microbial Sensitivity Tests
  • Middle Aged
  • Mortality
  • Mutation
  • Prevalence
  • Prognosis
  • Retrospective Studies
  • Survival Analysis
  • Voriconazole / pharmacology*
  • Voriconazole / therapeutic use

Substances

  • Antifungal Agents
  • Fungal Proteins
  • Cytochrome P-450 Enzyme System
  • cytochrome P-450 CYP51A, Aspergillus
  • Voriconazole