Literature DB >> 20646968

Design and powering of cystic fibrosis clinical trials using rate of FEV(1) decline as an efficacy endpoint.

M W Konstan1, J S Wagener, A Yegin, S J Millar, D J Pasta, D R VanDevanter.   

Abstract

BACKGROUND: Rate of lung function decline (RLFD) (as FEV(1) percent predicted/yr) is a robust measure of CF therapeutic efficacy rarely used as a study endpoint, in part due to uncertainty of sample size requirements.
METHODS: Sample size requirements for 1:1 randomizations to detect RLFD treatment effects from 20% to 80% were assessed in Epidemiologic Study of CF (ESCF) patients. Effects of measuring FEV(1) 1-4 times per year in studies of 1- to 4-year durations were assessed in 399 patients age ≥ 6 years with FEV(1) ≥ 70%. Impacts of inclusion/exclusion based on risk factors in 2369 ESCF patients were assessed over 1.5 years using semi-annual FEV(1) measures.
RESULTS: Increasing study duration and exclusion of lower risk patients (e.g., no P. aeruginosa infection) both substantially reduced requirements.
CONCLUSIONS: CF RLFD studies of 1.5 years in duration appear feasible provided that investigators account for the beneficial effects of subject inclusion/exclusion based on risk factors in power estimates.
Copyright © 2010 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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Mesh:

Year:  2010        PMID: 20646968      PMCID: PMC4079112          DOI: 10.1016/j.jcf.2010.05.004

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


  16 in total

1.  Spirometric reference values from a sample of the general U.S. population.

Authors:  J L Hankinson; J R Odencrantz; K B Fedan
Journal:  Am J Respir Crit Care Med       Date:  1999-01       Impact factor: 21.405

2.  Epidemiologic study of cystic fibrosis: design and implementation of a prospective, multicenter, observational study of patients with cystic fibrosis in the U.S. and Canada.

Authors:  W J Morgan; S M Butler; C A Johnson; A A Colin; S C FitzSimmons; D E Geller; M W Konstan; M J Light; H R Rabin; W E Regelmann; D V Schidlow; D C Stokes; M E Wohl; H Kaplowitz; M M Wyatt; S Stryker
Journal:  Pediatr Pulmonol       Date:  1999-10

3.  A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis.

Authors:  Mark R Elkins; Michael Robinson; Barbara R Rose; Colin Harbour; Carmel P Moriarty; Guy B Marks; Elena G Belousova; Wei Xuan; Peter T P Bye
Journal:  N Engl J Med       Date:  2006-01-19       Impact factor: 91.245

4.  Identifying treatments that halt progression of pulmonary disease in cystic fibrosis.

Authors:  P B Davis; P J Byard; M W Konstan
Journal:  Pediatr Res       Date:  1997-02       Impact factor: 3.756

5.  Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis.

Authors:  M Corey; L Edwards; H Levison; M Knowles
Journal:  J Pediatr       Date:  1997-12       Impact factor: 4.406

6.  Clinical use of Ibuprofen is associated with slower FEV1 decline in children with cystic fibrosis.

Authors:  Michael W Konstan; Mark D Schluchter; Wei Xue; Pamela B Davis
Journal:  Am J Respir Crit Care Med       Date:  2007-09-13       Impact factor: 21.405

7.  Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group.

Authors:  B W Ramsey; M S Pepe; J M Quan; K L Otto; A B Montgomery; J Williams-Warren; M Vasiljev-K; D Borowitz; C M Bowman; B C Marshall; S Marshall; A L Smith
Journal:  N Engl J Med       Date:  1999-01-07       Impact factor: 91.245

8.  Effect of high-dose ibuprofen in patients with cystic fibrosis.

Authors:  M W Konstan; P J Byard; C L Hoppel; P B Davis
Journal:  N Engl J Med       Date:  1995-03-30       Impact factor: 91.245

9.  Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group.

Authors:  H J Fuchs; D S Borowitz; D H Christiansen; E M Morris; M L Nash; B W Ramsey; B J Rosenstein; A L Smith; M E Wohl
Journal:  N Engl J Med       Date:  1994-09-08       Impact factor: 91.245

10.  Pulmonary function between 6 and 18 years of age.

Authors:  X Wang; D W Dockery; D Wypij; M E Fay; B G Ferris
Journal:  Pediatr Pulmonol       Date:  1993-02
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  17 in total

Review 1.  Building global development strategies for cf therapeutics during a transitional cftr modulator era.

Authors:  N Mayer-Hamblett; S van Koningsbruggen-Rietschel; D P Nichols; D R VanDevanter; J C Davies; T Lee; A G Durmowicz; F Ratjen; M W Konstan; K Pearson; S C Bell; J P Clancy; J L Taylor-Cousar; K De Boeck; S H Donaldson; D G Downey; P A Flume; P Drevinek; C H Goss; I Fajac; A S Magaret; B S Quon; S M Singleton; J M VanDalfsen; G Z Retsch-Bogart
Journal:  J Cyst Fibros       Date:  2020-06-07       Impact factor: 5.482

2.  Parents as equal partners in the paediatric cystic fibrosis multidisciplinary team.

Authors:  Mandy Bryon; Colin Wallis
Journal:  J R Soc Med       Date:  2011-07       Impact factor: 5.344

3.  Longitudinal association between medication adherence and lung health in people with cystic fibrosis.

Authors:  Michelle N Eakin; Andrew Bilderback; Michael P Boyle; Peter J Mogayzel; Kristin A Riekert
Journal:  J Cyst Fibros       Date:  2011-03-31       Impact factor: 5.482

4.  Effect of dornase alfa on inflammation and lung function: potential role in the early treatment of cystic fibrosis.

Authors:  Michael W Konstan; Felix Ratjen
Journal:  J Cyst Fibros       Date:  2011-11-16       Impact factor: 5.482

Review 5.  Omics approaches in cystic fibrosis research: a focus on oxylipin profiling in airway secretions.

Authors:  Jason P Eiserich; Jun Yang; Brian M Morrissey; Bruce D Hammock; Carroll E Cross
Journal:  Ann N Y Acad Sci       Date:  2012-07       Impact factor: 5.691

6.  Empire-CF study: A phase 2 clinical trial of leukotriene A4 hydrolase inhibitor acebilustat in adult subjects with cystic fibrosis.

Authors:  J Stuart Elborn; Michael W Konstan; Jennifer L Taylor-Cousar; Isabelle Fajac; Alexander Horsley; Sivagurunathan Sutharsan; Shawn D Aaron; Cori L Daines; Ahmet Uluer; Damian G Downey; Vincenzina V Lucidi; Sanjeev Ahuja; Eric Springman; John Mershon; Ralph Grosswald; Steven M Rowe
Journal:  J Cyst Fibros       Date:  2021-09-17       Impact factor: 5.482

7.  Risk factors for rate of decline in FEV1 in adults with cystic fibrosis.

Authors:  Michael W Konstan; Jeffrey S Wagener; Donald R Vandevanter; David J Pasta; Ashley Yegin; Lawrence Rasouliyan; Wayne J Morgan
Journal:  J Cyst Fibros       Date:  2012-05-05       Impact factor: 5.482

8.  Metabolomic profiling of regulatory lipid mediators in sputum from adult cystic fibrosis patients.

Authors:  Jun Yang; Jason P Eiserich; Carroll E Cross; Brian M Morrissey; Bruce D Hammock
Journal:  Free Radic Biol Med       Date:  2012-05-08       Impact factor: 7.376

9.  Outcome measures for clinical trials assessing treatment of cystic fibrosis lung disease.

Authors:  Donald R VanDevanter; Michael W Konstan
Journal:  Clin Investig (Lond)       Date:  2012

Review 10.  Epidemiologic Study of Cystic Fibrosis: 25 years of observational research.

Authors:  Michael W Konstan; David J Pasta; Donald R VanDevanter; Jeffrey S Wagener; Wayne J Morgan
Journal:  Pediatr Pulmonol       Date:  2021-01-12
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