Literature DB >> 21803665

Design and powering of cystic fibrosis clinical trials using pulmonary exacerbation as an efficacy endpoint.

D R Vandevanter1, A Yegin, W J Morgan, S J Millar, D J Pasta, M W Konstan.   

Abstract

BACKGROUND: Reduction in pulmonary exacerbations is an important efficacy endpoint for CF clinical studies. Powering exacerbation endpoints requires estimation of the future exacerbation incidence in CF study populations, but rates differ across the population.
METHODS: We have estimated exacerbation rates for Epidemiologic Study of CF subpopulations stratified by age, FEV(1)% predicted, sex, weight-for-age percentile, respiratory signs and symptoms, and history of exacerbation and bacterial culture. Sample sizes required to attain 80% power to detect exacerbation reductions of 20% to 80% in 1:1 randomized studies of 3 to 12 month duration were determined. Exacerbation treatments with "any" antibiotic (new oral quinolone, new inhaled antibiotic, or intravenous (IV) antibiotic) and with IV antibiotics were studied.
RESULTS: At all ages, decreased FEV(1), female sex, exacerbation history, and Pseudomonas aeruginosa culture history were associated with increased treatment for exacerbation.
CONCLUSIONS: These data should assist investigators in the design of future CF exacerbation studies.
Copyright © 2011 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21803665      PMCID: PMC4079110          DOI: 10.1016/j.jcf.2011.07.003

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


  29 in total

1.  Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease.

Authors:  Timothy D Murphy; Ran D Anbar; Lucille A Lester; Samya Z Nasr; Bruce Nickerson; Donald R VanDevanter; Andrew A Colin
Journal:  Pediatr Pulmonol       Date:  2004-10

Review 2.  Management of pulmonary disease in patients with cystic fibrosis.

Authors:  B W Ramsey
Journal:  N Engl J Med       Date:  1996-07-18       Impact factor: 91.245

3.  Developing cystic fibrosis lung transplant referral criteria using predictors of 2-year mortality.

Authors:  Nicole Mayer-Hamblett; Margaret Rosenfeld; Julia Emerson; Christopher H Goss; Moira L Aitken
Journal:  Am J Respir Crit Care Med       Date:  2002-08-15       Impact factor: 21.405

4.  Quality of well-being before and after antibiotic treatment of pulmonary exacerbation in patients with cystic fibrosis.

Authors:  D M Orenstein; E N Pattishall; P A Nixon; E A Ross; R M Kaplan
Journal:  Chest       Date:  1990-11       Impact factor: 9.410

5.  Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial.

Authors:  Lisa Saiman; Bruce C Marshall; Nicole Mayer-Hamblett; Jane L Burns; Alexandra L Quittner; Debra A Cibene; Sarah Coquillette; Ann Yunker Fieberg; Frank J Accurso; Preston W Campbell
Journal:  JAMA       Date:  2003-10-01       Impact factor: 56.272

6.  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

7.  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

8.  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

9.  Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients.

Authors:  Tim W R Lee; Keith G Brownlee; Steven P Conway; Miles Denton; James M Littlewood
Journal:  J Cyst Fibros       Date:  2003-03       Impact factor: 5.482

10.  Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis.

Authors:  Julia Emerson; Margaret Rosenfeld; Sharon McNamara; Bonnie Ramsey; Ronald L Gibson
Journal:  Pediatr Pulmonol       Date:  2002-08
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  16 in total

Review 1.  Innovating cystic fibrosis clinical trial designs in an era of successful standard of care therapies.

Authors:  Donald R VanDevanter; Nicole Mayer-Hamblett
Journal:  Curr Opin Pulm Med       Date:  2017-11       Impact factor: 3.155

2.  Anti-PcrV antibody in cystic fibrosis: a novel approach targeting Pseudomonas aeruginosa airway infection.

Authors:  Carlos E Milla; James F Chmiel; Frank J Accurso; Donald R VanDevanter; Michael W Konstan; Geoffrey Yarranton; David E Geller
Journal:  Pediatr Pulmonol       Date:  2013-09-09

3.  Treatment and demographic factors affecting time to next pulmonary exacerbation in cystic fibrosis.

Authors:  Donald R VanDevanter; David J Pasta; Michael W Konstan
Journal:  J Cyst Fibros       Date:  2015-03-06       Impact factor: 5.482

4.  Chest computed tomography predicts the frequency of pulmonary exacerbations in children with cystic fibrosis.

Authors:  Don B Sanders; Zhanhai Li; Alan S Brody
Journal:  Ann Am Thorac Soc       Date:  2015-01

5.  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

6.  IV-treated pulmonary exacerbations in the prior year: An important independent risk factor for future pulmonary exacerbation in cystic fibrosis.

Authors:  Donald R VanDevanter; Nathan J Morris; Michael W Konstan
Journal:  J Cyst Fibros       Date:  2015-10-23       Impact factor: 5.482

7.  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 8.  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

Review 9.  Treatment of Pulmonary Disease of Cystic Fibrosis: A Comprehensive Review.

Authors:  Rosa María Girón Moreno; Marta García-Clemente; Layla Diab-Cáceres; Adrián Martínez-Vergara; Miguel Ángel Martínez-García; Rosa Mar Gómez-Punter
Journal:  Antibiotics (Basel)       Date:  2021-04-23

10.  A new path for CF clinical trials through the use of historical controls.

Authors:  Amalia S Magaret; Mark Warden; Noah Simon; Sonya Heltshe; George Z Retsch-Bogart; Bonnie W Ramsey; Nicole Mayer-Hamblett
Journal:  J Cyst Fibros       Date:  2021-12-05       Impact factor: 5.482

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