4.3 Article

Evaluating assumptions of definition-based pulmonary exacerbation endpoints in cystic fibrosis clinical trials

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JOURNAL OF CYSTIC FIBROSIS
卷 20, 期 1, 页码 39-45

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ELSEVIER
DOI: 10.1016/j.jcf.2020.07.008

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  1. Cystic Fibrosis Foundation
  2. National Institutes of Health [P30 DK 089507, UL1 TR002319, P01 HL128192, UL1 TR002548]

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The study compared respiratory events (RE) observed during a 48-week trial of ataluren across six exacerbation definitions. It found that missingness of criteria in Fuchs definitions and the presence of criteria were associated with clinician exacerbation assessment.
Background: Cystic fibrosis (CF) pulmonary exacerbations can be serious respiratory events and reduction in exacerbation rate or risk are important efficacy endpoints for CF therapeutic trials. Variability in exacerbation diagnoses and treatment have led drug developers to employ objective exacerbation definitions combining antimicrobial treatment (AT) and the presence of >= 4 of 12 respiratory criteria (first published by Fuchs et al. [NEJM 1994;331(10):637-42]). Assumptions underlying this approach have yet to be formally evaluated. Methods: Respiratory events (RE) observed during a 48-week trial of ataluren (NCT02139306), a read through agent for premature nonsense codons, were compared across six exacerbation definitions: any AT, intravenous AT (IVAT), >= 4 Fuchs criteria present, AT plus >= 4 Fuchs criteria, IVAT plus >= 4 Fuchs criteria, and investigator assessment. Fuchs definitions were evaluated by assessing missingness of individual criteria and associations between criteria presence and clinician exacerbation assessment. Results: Among 751 RE, more than one third had >= 4 Fuchs criteria present but were not assessed as exacerbations by investigators. Data for >= 1 and for 4 Fuchs criteria, respectively, were missing for similar to 90% and > 30% of RE. Only 6/12 Fuchs criteria were present more often when investigators assessed RE as exacerbations than when they did not. Conclusions: Objective definitions have shortcomings inconsistent with their purpose of optimizing exacerbation capture in clinical trials : 1) they capture events clinicians do not consider exacerbations, 2) are prone to data missingness which can bias the likelihood of meeting the definition, and 3) employ criteria that are not associated with investigator assessment of exacerbation. (C) 2020 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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