» Articles » PMID: 35721187

Elexacaftor-Tezacaftor-Ivacaftor Treatment Reduces Abdominal Symptoms in Cystic Fibrosis-Early Results Obtained With the CF-Specific CFAbd-Score

Abstract

The novel and highly effective CFTR modulator combination of elexacaftor-tezacaftor-ivacaftor (ETI) has been shown to improve lung function and body weight in people with Cystic Fibrosis (pwCF) carrying a F508del mutation. However, the impact of these modulators on gastrointestinal (GI) symptoms is relatively unknown. Therefore, the CFAbd-Score was developed and validated following FDA recommendations for development of a PROM including focus groups, multidisciplinary CF specialists, people with CF and their families. The aim of this study was to assess effects of ETI on GI symptoms using the CFAbd-Score. Gastrointestinal symptoms were prospectively assessed in pwCF using the CFAbd-Score before and up to 26 weeks during therapy. The CFAbd-Score was also administered to a healthy control (HC) group. The one-sided questionnaire includes 28 items grouped in five domains. Data analysis included calculation of scores with a weighting tool, developed according to FDA recommendations. A total of 107 pwCF attended in four CF centres in Germany and four centres in the UK completed the CFAbd-Score on at least two occasions. Results were compared to those obtained from the questionnaire of 45 HCs. Despite differences in demographics, age and proportion of pancreatic insufficiency between German and UK patients, analyses based on linear mixed-effects models at week 24 of ETI therapy revealed that estimated marginal means (EMMs) of total CFAbd-Scores significantly reduced (mean ± SE: 14.9 ± 1.2→10.6 ± 1.4; < 0.01). Also EMMs of all five domains significantly declined ("pain" 16.3 ± 1.6→10.2 ± 2.3, "GERD" 15.8 ± 1.8→8.2 ± 1.9, "disorders of bowel movement" 20.9 ± 1.5→16.0 ± 1.7, "disorders of appetite" 7.9 ± 1.1→2.6 ± 1.1 and "quality of life impairment" 10.1 ± 1.92→3.9 ± 1.9). However, during 24 weeks, CF participants' symptoms mostly still did not reach the reference levels of HCs. Using the CFAbd-Score, the first PROM specifically developed for assessment of CF-related abdominal symptoms, we demonstrate comprehensive improvements in GI symptoms after initiation of the highly effective modulator therapy ETI.

Citing Articles

The Dutch Gastrointestinal Symptom Tracker for People With Cystic Fibrosis: Associations With Anxiety, Depression, and Health-Related Quality of Life.

Verkleij M, Vlieg-Boerstra B, Hofsteenge G, Haarman E, Twisk J, Quittner A Pediatr Pulmonol. 2025; 60(3):e71021.

PMID: 40019138 PMC: 11869532. DOI: 10.1002/ppul.71021.


A randomised crossover trial of tezacaftor-ivacaftor for gut dysfunction in cystic fibrosis with magnetic resonance imaging (MRI) outcomes: a pilot study.

Ng C, Dellschaft N, Hoad C, Marciani L, Spiller R, Crooks C NIHR Open Res. 2024; 3:65.

PMID: 39139270 PMC: 11320032. DOI: 10.3310/nihropenres.13510.2.


Elexacaftor-tezacaftor-ivacaftor use after solid organ transplant.

Kapnadak S, Ramos K Curr Opin Pulm Med. 2024; 30(6):660-666.

PMID: 39082904 PMC: 11611685. DOI: 10.1097/MCP.0000000000001110.


Impaired intestinal free fatty acid transport followed by chylomicron malformation, not pancreatic insufficiency, cause metabolic defects in cystic fibrosis.

Teng L, Dedousis N, Adeshirlarijaney A, Kanshana J, Liu M, Hodges C J Lipid Res. 2024; 65(7):100551.

PMID: 39002195 PMC: 11301217. DOI: 10.1016/j.jlr.2024.100551.


Scoring Abdominal Symptoms in People with Cystic Fibrosis.

Tabori H, Barucha A, Zagoya C, Duckstein F, Dunay G, Sadrieh P J Clin Med. 2024; 13(6).

PMID: 38541878 PMC: 10971656. DOI: 10.3390/jcm13061650.


References
1.
Davies J, Wainwright C, Canny G, Chilvers M, Howenstine M, Munck A . Efficacy and safety of ivacaftor in patients aged 6 to 11 years with cystic fibrosis with a G551D mutation. Am J Respir Crit Care Med. 2013; 187(11):1219-25. PMC: 3734608. DOI: 10.1164/rccm.201301-0153OC. View

2.
Wainwright C, Elborn J, Ramsey B, Marigowda G, Huang X, Cipolli M . Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR. N Engl J Med. 2015; 373(3):220-31. PMC: 4764353. DOI: 10.1056/NEJMoa1409547. View

3.
Raun A, Brekke G, Molgaard C, Jaudszus A, Mainz J, Pressler T . Impact of timing of PERT on gastrointestinal symptoms in Danish children and adolescents with CF. Acta Paediatr. 2021; 111(2):432-439. DOI: 10.1111/apa.16143. View

4.
Balfour-Lynn I, King J . CFTR modulator therapies - Effect on life expectancy in people with cystic fibrosis. Paediatr Respir Rev. 2020; 42:3-8. PMC: 7255286. DOI: 10.1016/j.prrv.2020.05.002. View

5.
Rosenfeld M, Wainwright C, Higgins M, Wang L, McKee C, Campbell D . Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study. Lancet Respir Med. 2018; 6(7):545-553. PMC: 6626762. DOI: 10.1016/S2213-2600(18)30202-9. View