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1000 Titel
  • Elexacaftor-Tezacaftor-Ivacaftor treatment reduces abdominal symptoms in cystic fibrosis -Early results obtained with the CF-specific CFAbd-Score
1000 Autor/in
  1. Mainz, Jochen G. |
  2. Zagoya, Carlos |
  3. Polte, Louise |
  4. Naehrlich, Lutz |
  5. Sasse, Lenny |
  6. Eickmeier, Olaf |
  7. Smaczny, Christina |
  8. Barucha, Anton |
  9. Bechinger, Lilith |
  10. Duckstein, Franziska |
  11. Kurzidim, Ludwik |
  12. Eschenhagen, Patience |
  13. Caley, Laura |
  14. Peckham, Daniel |
  15. Schwarz, Carsten |
1000 Erscheinungsjahr 2022
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2022-06-03
1000 Erschienen in
1000 Quellenangabe
  • 13: 877118
1000 FRL-Sammlung
1000 Copyrightjahr
  • 2022
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3389/fphar.2022.877118 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203829/ |
1000 Ergänzendes Material
  • https://www.frontiersin.org/articles/10.3389/fphar.2022.877118/full#h13 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • BACKGROUND: 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. METHODS: 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. RESULTS: 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; p < 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. DISCUSSION: 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. KEYWORDS: gastrointestinal, patient reported outcome measure, CFTR modulators, elexacaftor, symptom score
1000 Sacherschließung
lokal patient reported outcome measure
lokal CFTR modulators
lokal elexacaftor
lokal gastrointestinal
lokal symptom score
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TWFpbnosIEpvY2hlbiBHLg==|https://frl.publisso.de/adhoc/uri/WmFnb3lhLCBDYXJsb3Mg|https://frl.publisso.de/adhoc/uri/UG9sdGUsIExvdWlzZSA=|https://frl.publisso.de/adhoc/uri/TmFlaHJsaWNoLCBMdXR6|https://frl.publisso.de/adhoc/uri/U2Fzc2UsIExlbm55|https://frl.publisso.de/adhoc/uri/RWlja21laWVyLCBPbGFm|https://frl.publisso.de/adhoc/uri/U21hY3pueSwgQ2hyaXN0aW5h|https://frl.publisso.de/adhoc/uri/QmFydWNoYSwgQW50b24=|https://frl.publisso.de/adhoc/uri/QmVjaGluZ2VyLCBMaWxpdGg=|https://frl.publisso.de/adhoc/uri/RHVja3N0ZWluLCBGcmFuemlza2E=|https://frl.publisso.de/adhoc/uri/S3VyemlkaW0sIEx1ZHdpaw==|https://frl.publisso.de/adhoc/uri/RXNjaGVuaGFnZW4sIFBhdGllbmNl|https://frl.publisso.de/adhoc/uri/Q2FsZXksIExhdXJh|https://frl.publisso.de/adhoc/uri/UGVja2hhbSwgRGFuaWVs|https://frl.publisso.de/adhoc/uri/U2Nod2FyeiwgQ2Fyc3Rlbg==
1000 Label
1000 Förderer
  1. Cystic Fibrosis Trust |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. SRC 012
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Cystic Fibrosis Trust |
    1000 Förderprogramm SRC 012
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6438598.rdf
1000 Erstellt am 2022-11-30T13:00:37.797+0100
1000 Erstellt von 324
1000 beschreibt frl:6438598
1000 Bearbeitet von 317
1000 Zuletzt bearbeitet 2022-12-21T08:58:13.373+0100
1000 Objekt bearb. Wed Dec 21 08:57:11 CET 2022
1000 Vgl. frl:6438598
1000 Oai Id
  1. oai:frl.publisso.de:frl:6438598 |
1000 Sichtbarkeit Metadaten public
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