Impact of Elexacaftor‐Tezacaftor‐Ivacaftor on Quality of Life in Children With Cystic Fibrosis
Sara Kümmerli, Clara Fernandez Elviro, Nicolas Regamey, Anne Mornand, Mohamed Faouzi, Isabelle Rochat, Sylvain Blanchon

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.
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…
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Taxonomy
TopicsCystic Fibrosis Research Advances · Child Nutrition and Feeding Issues · Immunodeficiency and Autoimmune Disorders
