Real-world 12-months outcomes after initiation of triple modulators in Australian cystic fibrosis population

In Australia, elexacaftor/tezacaftor/ivacaftor (ETI) was approved in April 2022 for people with cystic fibrosis (pwCF) ≥ 12 years of age. We investigated the effect of ETI on Australian pwCF by comparing changes in lung function (FEV1pp), use of intravenous antibiotics, and adverse events over the 12 months before and after ETI treatment. PwCF were categorised into four groups: (1) those on a full ETI dose, (2) those on a partial dose; (3) those who ceased ETI, and (4) those who switched to another CF transmembrane conductance regulator modulator (CFTRm). Descriptive statistics were used to describe the population, health service use and adverse events. The change in FEV1pp was compared using t tests and linear regressions. Data from 2,073 pwCF were analysed (1,100 (53.1%) male, 1,145 (55.2%) F508del homozygous). 1,833 (88.4%) participants were on a full dose, 97 (4.7%) on partial, 117 (5.6%) ceased ETI and 26 (1.3%) switched to another CFTRm. The greatest improvement in FEV1pp was observed in those on full and partial doses, with a mean (SD) change of 8.1% (9.2) and 8.6% (9.0) respectively. Post-ETI healthcare utilisation differed across ETI treatment groups after adjustment for pre-ETI utilisation and baseline characteristics, with generally higher clinic visit, hospitalisation and hospital IVAB utilisation among participants who did not remain on full-dose ETI. While ETI was generally well tolerated, approximately 12% of pwCF did not maintain a full dose due to side effects.

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Journal
BMC Pulmonary Medicine
Published
2026-09-10
DOI
https://doi.org/10.1186/s12890-026-04681-6
Primary Topic
Cystic Fibrosis Research Advances
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article
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article

Real-world 12-months outcomes after initiation of triple modulators in Australian cystic fibrosis population

André Schultz, Rasa Ruseckaite, Susannah Ahern, Bernadette Prentice et al.
BMC Pulmonary Medicine
Cystic Fibrosis Research Advances
article

Real-world 12-months outcomes after initiation of triple modulators in Australian cystic fibrosis population

André Schultz, Rasa Ruseckaite, Susannah Ahern, Bernadette Prentice, Peter Wark, Siobhain Mulrennan, Judith Morton, Katherine Frayman, Ahmad Reza Pourhaderi, Nathan Ward, Jo Armstrong
article en

Abstract

In Australia, elexacaftor/tezacaftor/ivacaftor (ETI) was approved in April 2022 for people with cystic fibrosis (pwCF) ≥ 12 years of age. We investigated the effect of ETI on Australian pwCF by comparing changes in lung function (FEV1pp), use of intravenous antibiotics, and adverse events over the 12 months before and after ETI treatment. PwCF were categorised into four groups: (1) those on a full ETI dose, (2) those on a partial dose; (3) those who ceased ETI, and (4) those who switched to another CF transmembrane conductance regulator modulator (CFTRm). Descriptive statistics were used to describe the population, health service use and adverse events. The change in FEV1pp was compared using t tests and linear regressions. Data from 2,073 pwCF were analysed (1,100 (53.1%) male, 1,145 (55.2%) F508del homozygous). 1,833 (88.4%) participants were on a full dose, 97 (4.7%) on partial, 117 (5.6%) ceased ETI and 26 (1.3%) switched to another CFTRm. The greatest improvement in FEV1pp was observed in those on full and partial doses, with a mean (SD) change of 8.1% (9.2) and 8.6% (9.0) respectively. Post-ETI healthcare utilisation differed across ETI treatment groups after adjustment for pre-ETI utilisation and baseline characteristics, with generally higher clinic visit, hospitalisation and hospital IVAB utilisation among participants who did not remain on full-dose ETI. While ETI was generally well tolerated, approximately 12% of pwCF did not maintain a full dose due to side effects.

BMC Pulmonary Medicine
Royal Adelaide Hospital (AU), Royal Children's Hospital (AU), The University of Melbourne (AU), The Kids Research Institute Australia (AU), Princess Margaret Hospital for Children (AU), Sir Charles Gairdner Hospital (AU), UNSW Sydney (AU), Sydney Children's Hospital (AU), Institute for Respiratory Health (AU), Murdoch Children's Research Institute (AU), Alfred Health (AU), Perth Children's Hospital, Monash University (AU)
Good health and well-being
Openalex Percentile: Top 11%
Cystic Fibrosis Research Advances
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