# Impact of Elexacaftor‐Tezacaftor‐Ivacaftor on Quality of Life in Children With Cystic Fibrosis

**Authors:** Sara Kümmerli, Clara Fernandez Elviro, Nicolas Regamey, Anne Mornand, Mohamed Faouzi, Isabelle Rochat, Sylvain Blanchon

PMC · DOI: 10.1002/ppul.71461 · 2026-01-07

## TL;DR

This study shows that the drug Elexacaftor-Tezacaftor-Ivacaftor significantly improves the quality of life for children with cystic fibrosis, especially in physical health.

## Contribution

The study provides new evidence on the impact of ETI on children's quality of life, particularly in physical domains.

## Key findings

- ETI significantly improved children's quality of life scores, especially in physical health domains.
- Children with the homozygous F508del genotype showed greater QoL improvement compared to others.
- Emotional, social, and school domains showed minimal improvement, highlighting the need for additional support.

## Abstract

CFTR modulators have revolutionized cystic fibrosis (CF) management by targeting the defective protein rather than its consequences. Their impact on quality of life (QoL) have been studied in numerous trials, but few data are available on QoL in patients receiving Elexacaftor‐Tezacaftor‐Ivacaftor (ETI), notably in children given its recent authorization for this age group. We aimed to assess the impact of ETI on children's QoL.

This prospective observational study included children with CF (6−17 years), assessing QoL using the CF Questionnaire Revised (CFQ‐R) before (baseline) and 3 months after (M3) starting ETI treatment for children and their caregivers.

We included 23 children (median [range]) age 10.2 [6−17.2] years, 13 (57%) with homozygous F508del genotype. The total QoL score at baseline ([mean (SD)] children: 74.07 [10.86]; caregivers: 73.21 [10.38]) reflected severe disease impact, particularly regarding treatment burden in the children's perspective (63.28 [21.04]) and digestive domains in the caregivers' perspective (digestive symptoms: 66.67 [17.37]; eating disorder: 67.54 [32.14]; weight: 61.40 [33.82]). At M3, there was a significant increase in reported QoL (p = 0.0001), particularly regarding physical domains. Emotional/social/school domains barely showed improvement. Although QoL mean scores were comparable between children and caregivers' groups, they were poorly correlated within the same family. Homozygous F508del genotype was associated with better QoL improvement at M3 compared to composite heterozygous genotypes (p < 0.001).

ETI treatment has a significant impact on children's QoL, particularly in physical health domains. Other QoL domains that are not improved by ETI need to be addressed, in particular, psycho‐social components. Both children's and caregivers' perspectives must be considered for a holistic picture of children's QoL.

## Linked entities

- **Genes:** CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080]
- **Chemicals:** Elexacaftor (PubChem CID 134587348), Tezacaftor (PubChem CID 46199646), Ivacaftor (PubChem CID 16220172)
- **Diseases:** cystic fibrosis (MONDO:0009061)

## Full-text entities

- **Genes:** CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}
- **Diseases:** digestive symptoms (MESH:D012817), eating disorder (MESH:D001068), CF (MESH:D003550)
- **Chemicals:** ETI (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** F508del

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12778892/full.md

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Source: https://tomesphere.com/paper/PMC12778892