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Wellness in the modulator era: An observational study of the impact of CFTR modulator therapy on the well-being of people with cystic fibrosis

  • Aricca D. Van Citters
  • , Enid Aliaj
  • , Jessica A. Alvarez
  • , Cynthia D. Brown
  • , Jamie Cary
  • , Rachel Cravens
  • , Carla A. Frederick
  • , Anna M. Georgiopoulos
  • , Christopher H. Goss
  • , Traci M. Kazmerski
  • , Joel R. King
  • , Melanie Lawrence
  • , Caitlyn Lovell
  • , Christina Roman
  • , Laura Tillman
  • , Elizabeth Yu
  • Dartmouth College
  • Cystic Fibrosis Foundation
  • Emory University
  • Indiana University Bloomington
  • MD
  • Massachusetts General Hospital
  • University of Washington
  • University of Pittsburgh

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Background: People with cystic fibrosis (PwCF) have experienced substantial improvements in health following use of cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies. However, less is known about how modulator therapies impact well-being. Methods: We used a cross-sectional observational study to identify relationships between CFTR modulator therapies, health-related quality of life (HRQoL), and well-being. Adult PwCF and caregivers of children with CF completed the Wellness in the Modulator Era (Well-ME) survey between June 22 and July 31, 2022. HRQoL was measured with PROMIS Global 10/Global 7 + 2 Parent Proxy. We used a mixed methods analysis to compare experiences and concerns of PwCF who currently (n = 665), no longer (n = 51), or never (n = 184) took modulator therapy. Results: Adult PwCF taking a modulator (n = 416) reported better PROMIS global physical health than those who no longer (n = 37) or never took a modulator (n = 94) and better PROMIS global mental health than those who never took a modulator. Caregiver-reported HRQoL was similar across children with CF who currently, no longer, or never took a modulator. PwCF taking a modulator reported larger improvements in physical health, quality of life, social well-being, and treatment burden than those who no longer or never took a modulator. Nearly one-quarter (23 %) of PwCF taking modulator therapy reported worsening of mental well-being. Conclusions: This study expands our knowledge of well-being among PwCF in the CFTR modulator era as reported by patients and parents. Findings lay the groundwork for establishing future research priorities, policy efforts, and communications in areas that improve well-being for PwCF.

Original languageEnglish
Pages (from-to)642-651
Number of pages10
JournalJournal of Cystic Fibrosis
Volume24
Issue number4
DOIs
StatePublished - Jul 2025

Keywords

  • CFTR modulator therapy
  • Cystic fibrosis
  • Quality of life
  • Well-being

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