Impact of lumacaftor/ivacaftor on the bacterial and fungal respiratory pathogens in cystic fibrosis: a prospective multicenter cohort study in Sweden

Ther Adv Respir Dis. 2024 Jan-Dec:18:17534666241254090. doi: 10.1177/17534666241254090.

Abstract

Background: A significant decline in pulmonary exacerbation rates has been reported in CF patients homozygous for F508del treated with lumacaftor/ivacaftor. However, it is still unclear whether this reduction reflects a diminished microbiological burden.

Objectives: The aim of this study was to determine the impact of lumacaftor/ivacaftor on the bacterial and fungal burden.

Design: The study is a prospective multicenter cohort study including 132 CF patients homozygous for F508del treated with lumacaftor/ivacaftor.

Methods: Clinical parameters as well as bacterial and fungal outcomes 1 year after initiation of lumacaftor/ivacaftor were compared to data from 2 years prior to initiation of the treatment. Changes in the slope of the outcomes before and after the onset of treatment were assessed.

Results: Lung function measured as ppFEV1 (p < 0.001), body mass index (BMI) in adults (p < 0.001), and BMI z-score in children (p = 0.007) were improved after initiation of lumacaftor/ivacaftor. In addition, the slope of the prevalence of Streptococcus pneumoniae (p = 0.007) and Stenotrophomonas maltophilia (p < 0.001) shifted from positive to negative, that is, became less prevalent, 1 year after treatment, while the slope for Candida albicans (p = 0.009), Penicillium spp (p = 0.026), and Scedosporium apiospermum (p < 0.001) shifted from negative to positive.

Conclusion: The current study showed a significant improvement in clinical parameters and a reduction of some of CF respiratory microorganisms 1 year after starting with lumacaftor/ivacaftor. However, no significant changes were observed for Pseudomonas aeruginosa, Staphylococcus aureus, or Aspergillus fumigatus, key pathogens in the CF context.

Keywords: bacteria; cystic fibrosis; fungi; lumacaftor/ivacaftor.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Aminophenols* / therapeutic use
  • Aminopyridines* / administration & dosage
  • Aminopyridines* / adverse effects
  • Aminopyridines* / pharmacology
  • Aminopyridines* / therapeutic use
  • Bacterial Infections / drug therapy
  • Bacterial Infections / microbiology
  • Benzodioxoles* / therapeutic use
  • Child
  • Chloride Channel Agonists / therapeutic use
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis* / drug therapy
  • Cystic Fibrosis* / microbiology
  • Cystic Fibrosis* / physiopathology
  • Drug Combinations*
  • Female
  • Fungi / isolation & purification
  • Humans
  • Lung / drug effects
  • Lung / microbiology
  • Lung / physiopathology
  • Male
  • Mycoses / drug therapy
  • Mycoses / microbiology
  • Prospective Studies
  • Quinolones* / pharmacology
  • Respiratory Tract Infections / diagnosis
  • Respiratory Tract Infections / drug therapy
  • Respiratory Tract Infections / microbiology
  • Sweden
  • Time Factors
  • Treatment Outcome
  • Young Adult

Substances

  • Aminophenols
  • Benzodioxoles
  • Drug Combinations
  • Aminopyridines
  • lumacaftor, ivacaftor drug combination
  • Quinolones
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • CFTR protein, human
  • Chloride Channel Agonists