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Observational Study
. 2018 Dec 13;52(6):1801444.
doi: 10.1183/13993003.01444-2018. Print 2018 Dec.

Randomised controlled trials in severe asthma: selection by phenotype or stereotype

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Free article
Observational Study

Randomised controlled trials in severe asthma: selection by phenotype or stereotype

Thomas Brown et al. Eur Respir J. .
Free article

Abstract

Previous publications have highlighted the disparity between research trial populations and those in clinical practice, but it has not been established how this relates to randomised controlled trials (RCTs) of phenotype-targeted biological therapies in severe asthma.Detailed characterisation data for 342 severe asthma patients within the Wessex Severe Asthma Cohort (WSAC) was compared against comprehensive trial eligibility criteria for published phase IIB and phase III RCTs evaluating biological therapies in severe asthma since 2000.37 RCTs evaluating 20 biological therapies were identified. Only a median of 9.8% (range 3.5-17.5%) of severe asthma patients were found to be eligible for enrolment in the phase III trials. Stipulations for airflow obstruction, bronchodilator reversibility and smoking history excluded significant numbers of patients. A median of 78.9% (range 73.2-86.6%) of patients with severe eosinophilic asthma would have been excluded from participation in the phase III licensing trials of interleukin (IL)-5/IL-5R targeted therapies.Despite including only well characterised and optimally treated severe asthmatics under specialist care within the WSAC study, the vast majority were excluded from trial participation by criteria designed to re-confirm diagnostic labels rather than by biomarker criteria that predict the characteristic addressed by the treatment.

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Conflict of interest statement

Conflict of interest: T. Brown reports personal fees from Teva, Chiesi Farmaceutici, Novartis and Napp, and non-financial support from AstraZeneca, outside the submitted work. T. Jones reports non-financial support from Teva, personal fees and non-financial support from Chiesi Farmaceutici, outside the submitted work. K. Gove has nothing to disclose. C. Barber has nothing to disclose. S. Elliott has nothing to disclose. Conflict of interest: A. Chauhan reports personal fees and non-financial support from Teva, non-financial support from Boehringer Ingelheim, and personal fees from AstraZeneca, outside the submitted work. Conflict of interest: P. Howarth reports grants from the Medical Research Council, during the conduct of the study; and is a part-time employee of GlaxoSmithKline.

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