Literature DB >> 34083123

Effect of lumacaftor-ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis: Results from the PROSPECT MCC sub-study.

Scott H Donaldson1, Beth L Laube2, Peter Mogayzel2, Timothy E Corcoran3, Joseph M Pilewski3, Agathe Ceppe4, Jihong Wu4, Pradeep G Bhambhvani5, Felix Ratjen6, Scott D Sagel7, J P Clancy8, Steven M Rowe5, William D Bennett4.   

Abstract

CFTR function is required for normal mucociliary clearance (MCC) and cough-assisted clearance (CC). Lumacaftor-ivacaftor is approved for use in people with cystic fibrosis (CF) carrying two copies of F508del-CFTR. In this observational study performed at four study sites, we characterized the effect of lumacaftor-ivacaftor on mucociliary and cough clearance and related this to other clinical and research endpoints after one month of treatment. Twenty-five adolescents and adults were enrolled. No effect on whole lung MCC was observed, but CC was significantly increased. Sweat chloride improved by 18 mEq/L in this group, indicating a modest restoration of CFTR activity, but no demonstrable change in FEV1 or lung clearance index was observed. We speculate that the modest effect of lumacaftor-ivacaftor on CFTR function was insufficient to yield an improvement in MCC.
Copyright © 2021 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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Year:  2021        PMID: 34083123      PMCID: PMC8630086          DOI: 10.1016/j.jcf.2021.05.004

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  20 in total

1.  Intestinal Current Measurements Detect Activation of Mutant CFTR in Patients with Cystic Fibrosis with the G551D Mutation Treated with Ivacaftor.

Authors:  Simon Y Graeber; Martin J Hug; Olaf Sommerburg; Stephanie Hirtz; Julia Hentschel; Andrea Heinzmann; Christian Dopfer; Angela Schulz; Jochen G Mainz; Burkhard Tümmler; Marcus A Mall
Journal:  Am J Respir Crit Care Med       Date:  2015-11-15       Impact factor: 21.405

2.  Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR.

Authors:  Scott H Donaldson; Beth L Laube; Timothy E Corcoran; Pradeep Bhambhvani; Kirby Zeman; Agathe Ceppe; Pamela L Zeitlin; Peter J Mogayzel; Michael Boyle; Landon W Locke; Michael M Myerburg; Joseph M Pilewski; Brian Flanagan; Steven M Rowe; William D Bennett
Journal:  JCI Insight       Date:  2018-12-20

3.  Multisite comparison of mucociliary and cough clearance measures using standardized methods.

Authors:  William D Bennett; Beth L Laube; Timothy Corcoran; Kirby Zeman; Gail Sharpless; Kristina Thomas; Jihong Wu; Peter J Mogayzel; Joseph Pilewski; Scott Donaldson
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2013-03-21       Impact factor: 2.849

4.  Consensus statement for inert gas washout measurement using multiple- and single- breath tests.

Authors:  Paul D Robinson; Philipp Latzin; Sylvia Verbanck; Graham L Hall; Alexander Horsley; Monika Gappa; Cindy Thamrin; Hubertus G M Arets; Paul Aurora; Susanne I Fuchs; Gregory G King; Sooky Lum; Kenneth Macleod; Manuel Paiva; Jane J Pillow; Sarath Ranganathan; Sarah Ranganathan; Felix Ratjen; Florian Singer; Samatha Sonnappa; Janet Stocks; Padmaja Subbarao; Bruce R Thompson; Per M Gustafsson
Journal:  Eur Respir J       Date:  2013-02-08       Impact factor: 16.671

5.  Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis.

Authors:  Steven M Rowe; Sonya L Heltshe; Tanja Gonska; Scott H Donaldson; Drucy Borowitz; Daniel Gelfond; Scott D Sagel; Umer Khan; Nicole Mayer-Hamblett; Jill M Van Dalfsen; Elizabeth Joseloff; Bonnie W Ramsey
Journal:  Am J Respir Crit Care Med       Date:  2014-07-15       Impact factor: 21.405

6.  A CFTR potentiator in patients with cystic fibrosis and the G551D mutation.

Authors:  Bonnie W Ramsey; Jane Davies; N Gerard McElvaney; Elizabeth Tullis; Scott C Bell; Pavel Dřevínek; Matthias Griese; Edward F McKone; Claire E Wainwright; Michael W Konstan; Richard Moss; Felix Ratjen; Isabelle Sermet-Gaudelus; Steven M Rowe; Qunming Dong; Sally Rodriguez; Karl Yen; Claudia Ordoñez; J Stuart Elborn
Journal:  N Engl J Med       Date:  2011-11-03       Impact factor: 91.245

7.  Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809.

Authors:  Fredrick Van Goor; Sabine Hadida; Peter D J Grootenhuis; Bill Burton; Jeffrey H Stack; Kimberly S Straley; Caroline J Decker; Mark Miller; Jason McCartney; Eric R Olson; Jeffrey J Wine; Ray A Frizzell; Melissa Ashlock; Paul A Negulescu
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-05       Impact factor: 11.205

8.  Clinical response to lumacaftor-ivacaftor in patients with cystic fibrosis according to baseline lung function.

Authors:  Pierre-Régis Burgel; Isabelle Durieu; Raphaël Chiron; Laurent Mely; Anne Prevotat; Marlene Murris-Espin; Michele Porzio; Michel Abely; Philippe Reix; Christophe Marguet; Julie Macey; Isabelle Sermet-Gaudelus; Harriet Corvol; Stéphanie Bui; Tiphaine Biouhee; Dominique Hubert; Anne Munck; Lydie Lemonnier; Clémence Dehillotte; Jennifer Da Silva; Jean-Louis Paillasseur; Clémence Martin
Journal:  J Cyst Fibros       Date:  2020-06-24       Impact factor: 5.482

9.  Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial.

Authors:  Scott D Sagel; Umer Khan; Sonya L Heltshe; John P Clancy; Drucy Borowitz; Daniel Gelfond; Scott H Donaldson; Antoinette Moran; Felix Ratjen; Jill M VanDalfsen; Steven M Rowe
Journal:  Ann Am Thorac Soc       Date:  2021-01

10.  Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation.

Authors:  Steven M Rowe; Bo Liu; Aubrey Hill; Heather Hathorne; Morty Cohen; John R Beamer; Frank J Accurso; Qunming Dong; Claudia L Ordoñez; Anne J Stone; Eric R Olson; John P Clancy
Journal:  PLoS One       Date:  2013-07-26       Impact factor: 3.240

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  2 in total

Review 1.  CFTR Modulators in People with Cystic Fibrosis: Real-World Evidence in France.

Authors:  Lucile Regard; Clémence Martin; Espérie Burnet; Jennifer Da Silva; Pierre-Régis Burgel
Journal:  Cells       Date:  2022-05-28       Impact factor: 7.666

2.  NBD2 Is Required for the Rescue of Mutant F508del CFTR by a Thiazole-Based Molecule: A Class II Corrector for the Multi-Drug Therapy of Cystic Fibrosis.

Authors:  Chiara Brandas; Alessandra Ludovico; Alice Parodi; Oscar Moran; Enrico Millo; Elena Cichero; Debora Baroni
Journal:  Biomolecules       Date:  2021-09-28
  2 in total

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