Literature DB >> 23845715

Clinimetric properties of bronchoalveolar lavage inflammatory markers in cystic fibrosis.

Michael Fayon1, Lisa Kent, Stephanie Bui, Lieven Dupont, Isabelle Sermet.   

Abstract

The Standardisation Committee of the European Cystic Fibrosis Society Clinical Trial Network has undertaken the evaluation of clinical end-points for therapeutic interventions regarding their use in multicentre clinical trials in cystic fibrosis (CF). This review of biomarkers in bronchoalveolar lavage (BAL) is part of the group's work. The aims of this project were: 1) to review the literature on reliability, validity and responsiveness of BAL in patients with CF; 2) to gain consensus of the group on the feasibility of BAL; and 3) to gain consensus on answers to key questions regarding the promotion of BAL to surrogate end-point status. Assessment of BAL inflammatory markers in the literature indicates that their reliability, validity and responsiveness are adequate for clinical trials. After discussion of the practical characteristics it was concluded that BAL has an attractive validity profile, albeit with limited feasibility. It is particularly applicable to multicentre trials in preschool children with CF and early or mild lung disease. This is the first article to collate the literature in this manner. This provides a rationale to support the use of BAL in early clinical trials in preschool children with CF.

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Year:  2013        PMID: 23845715     DOI: 10.1183/09031936.00017713

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   33.795


  7 in total

Review 1.  Mapping targetable inflammation and outcomes with cystic fibrosis biomarkers.

Authors:  Olivia Giddings; Charles R Esther
Journal:  Pediatr Pulmonol       Date:  2017-07-17

Review 2.  Biomarkers for cystic fibrosis drug development.

Authors:  Marianne S Muhlebach; J P Clancy; Sonya L Heltshe; Assem Ziady; Tom Kelley; Frank Accurso; Joseph Pilewski; Nicole Mayer-Hamblett; Elizabeth Joseloff; Scott D Sagel
Journal:  J Cyst Fibros       Date:  2016-10-27       Impact factor: 5.482

Review 3.  Cystic fibrosis: a clinical view.

Authors:  Carlo Castellani; Baroukh M Assael
Journal:  Cell Mol Life Sci       Date:  2016-10-05       Impact factor: 9.261

4.  Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis.

Authors:  Camilla Margaroli; Luke W Garratt; Hamed Horati; A Susanne Dittrich; Timothy Rosenow; Samuel T Montgomery; Dario L Frey; Milton R Brown; Carsten Schultz; Lokesh Guglani; Anthony Kicic; Limin Peng; Bob J Scholte; Marcus A Mall; Hettie M Janssens; Stephen M Stick; Rabindra Tirouvanziam
Journal:  Am J Respir Crit Care Med       Date:  2019-04-01       Impact factor: 21.405

5.  Chronic bacterial pulmonary infections in advanced cystic fibrosis differently affect the level of sputum neutrophil elastase, IL-8 and IL-6.

Authors:  Grzegorz Majka; Henryk Mazurek; Magdalena Strus; Marta Ciszek-Lenda; Rafał Szatanek; Agnieszka Pac; Edyta Golińska; Janusz Marcinkiewicz
Journal:  Clin Exp Immunol       Date:  2021-06-16       Impact factor: 5.732

6.  Disease-specific clinical trials networks: the example of cystic fibrosis.

Authors:  Kris De Boeck; Veerle Bulteel; Isabelle Fajac
Journal:  Eur J Pediatr       Date:  2016-03-15       Impact factor: 3.183

7.  Evaluation of autophagy inducers in epithelial cells carrying the ΔF508 mutation of the cystic fibrosis transmembrane conductance regulator CFTR.

Authors:  Shaoyi Zhang; Gautier Stoll; José Manuel Bravo San Pedro; Valentina Sica; Allan Sauvat; Florine Obrist; Oliver Kepp; Yousheng Li; Luigi Maiuri; Naoufal Zamzami; Guido Kroemer
Journal:  Cell Death Dis       Date:  2018-02-07       Impact factor: 8.469

  7 in total

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