Literature DB >> 35300931

Elexacaftor-Tezacaftor- Ivacaftor improves sinonasal outcomes in cystic fibrosis.

Amanda L Stapleton1, Adam J Kimple2, Jennifer L Goralski3, S Mehdi Nouraie4, Barton F Branstetter5, Amber D Shaffer1, Joseph M Pilewski4, Brent A Senior2, Stella E Lee1, Anna C Zemke4.   

Abstract

BACKGROUND: Many individuals with cystic fibrosis (CF) have chronic rhinosinusitis resulting in nasal obstruction, sinus infections, and repeated surgeries. Elexacaftor-tezacaftor-ivacaftor is a highly effective modulator therapy approved for individuals aged 6 years or older with CF who have at least one F508del allele or other responsive mutation. The current study tests the hypothesis that ELX/TEZ/IVA improves sinonasal disease in CF.
METHODS: The study was a pre/post, observational cohort study conducted at two sites. Participants underwent a study visit prior to starting ELX/TEZ/IVA and a second visit at a median of 9 months on therapy. Each visit included sinus CT scan, rigid nasal endoscopy, and sweat chloride measurement. Symptoms were measured with the 22 item Sinonasal Outcome Test at scheduled intervals during the study. Regression models were used to test for improvement in symptoms, endoscopy, and CT scales.
RESULTS: The study enrolled 34 individuals, with a median age of 27 years (range 12-60). Symptoms improved within 7 days of therapy and plateaued by day 28. Endoscopic crusting resolved and nasal polyposis improved, with a decrease in size or resolution of polyps. Sinus opacification and mucosal thickening improved on CT radiographs with treatment.
CONCLUSIONS: Sinonasal symptoms improved rapidly and durably for at least 180 days on ELX/TEZ/IVA therapy. Objective measures of disease including endoscopic and CT findings improved with ELX/TEZ/IVA.
Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; Highly effective modulator therapy; Sinus disease; Sinusitis

Year:  2022        PMID: 35300931      PMCID: PMC9470769          DOI: 10.1016/j.jcf.2022.03.002

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.527


  22 in total

1.  Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor.

Authors:  Eugene H Chang; Xiao Xiao Tang; Viral S Shah; Janice L Launspach; Sarah E Ernst; Brieanna Hilkin; Philip H Karp; Mahmoud H Abou Alaiwa; Scott M Graham; Douglas B Hornick; Michael J Welsh; David A Stoltz; Joseph Zabner
Journal:  Int Forum Allergy Rhinol       Date:  2014-10-31       Impact factor: 3.858

2.  Patterns of sinusitis in cystic fibrosis.

Authors:  V G Gentile; G Isaacson
Journal:  Laryngoscope       Date:  1996-08       Impact factor: 3.325

3.  Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

Authors:  Paul A Harris; Robert Taylor; Robert Thielke; Jonathon Payne; Nathaniel Gonzalez; Jose G Conde
Journal:  J Biomed Inform       Date:  2008-09-30       Impact factor: 6.317

4.  CT of the paranasal sinuses is not a valid indicator for sinus surgery in CF patients.

Authors:  Jacob Rasmussen; Kasper Aanæs; Rikke Norling; Kim G Nielsen; Helle Krogh Johansen; Christian von Buchwald
Journal:  J Cyst Fibros       Date:  2011-10-20       Impact factor: 5.482

5.  Importance to question sinonasal symptoms and to perform rhinoscopy and rhinomanometry in cystic fibrosis patients.

Authors:  J M Bock; M Schien; C Fischer; L Naehrlich; M Kaeding; O Guntinas-Lichius; A Gerber; C Arnold; J G Mainz
Journal:  Pediatr Pulmonol       Date:  2016-11-28

6.  International Consensus Statement on Allergy and Rhinology: Allergic Rhinitis.

Authors:  Sarah K Wise; Sandra Y Lin; Elina Toskala; Richard R Orlandi; Cezmi A Akdis; Jeremiah A Alt; Antoine Azar; Fuad M Baroody; Claus Bachert; G Walter Canonica; Thomas Chacko; Cemal Cingi; Giorgio Ciprandi; Jacquelynne Corey; Linda S Cox; Peter Socrates Creticos; Adnan Custovic; Cecelia Damask; Adam DeConde; John M DelGaudio; Charles S Ebert; Jean Anderson Eloy; Carrie E Flanagan; Wytske J Fokkens; Christine Franzese; Jan Gosepath; Ashleigh Halderman; Robert G Hamilton; Hans Jürgen Hoffman; Jens M Hohlfeld; Steven M Houser; Peter H Hwang; Cristoforo Incorvaia; Deborah Jarvis; Ayesha N Khalid; Maritta Kilpeläinen; Todd T Kingdom; Helene Krouse; Desiree Larenas-Linnemann; Adrienne M Laury; Stella E Lee; Joshua M Levy; Amber U Luong; Bradley F Marple; Edward D McCoul; K Christopher McMains; Erik Melén; James W Mims; Gianna Moscato; Joaquim Mullol; Harold S Nelson; Monica Patadia; Ruby Pawankar; Oliver Pfaar; Michael P Platt; William Reisacher; Carmen Rondón; Luke Rudmik; Matthew Ryan; Joaquin Sastre; Rodney J Schlosser; Russell A Settipane; Hemant P Sharma; Aziz Sheikh; Timothy L Smith; Pongsakorn Tantilipikorn; Jody R Tversky; Maria C Veling; De Yun Wang; Marit Westman; Magnus Wickman; Mark Zacharek
Journal:  Int Forum Allergy Rhinol       Date:  2018-02       Impact factor: 3.858

Review 7.  Staging for rhinosinusitis.

Authors:  V J Lund; D W Kennedy
Journal:  Otolaryngol Head Neck Surg       Date:  1997-09       Impact factor: 5.591

8.  Pulmonary aspiration of sinus secretions in patients with cystic fibrosis.

Authors:  Jacob Nelson; Peter Karempelis; Jordan Dunitz; Ryan Hunter; Holly Boyer
Journal:  Int Forum Allergy Rhinol       Date:  2017-12-06       Impact factor: 3.858

9.  The delta F508 mutation in cystic fibrosis and impact on sinus development.

Authors:  Bradford A Woodworth; Chadwick Ahn; Patrick A Flume; Rodney J Schlosser
Journal:  Am J Rhinol       Date:  2007 Jan-Feb

10.  The upper respiratory tract as a microbial source for pulmonary infections in cystic fibrosis. Parallels from island biogeography.

Authors:  Katrine L Whiteson; Barbara Bailey; Megan Bergkessel; Douglas Conrad; Laurence Delhaes; Ben Felts; J Kirk Harris; Ryan Hunter; Yan Wei Lim; Heather Maughan; Robert Quinn; Peter Salamon; James Sullivan; Brandie D Wagner; Paul B Rainey
Journal:  Am J Respir Crit Care Med       Date:  2014-06-01       Impact factor: 21.405

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