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Treatable Trait Guided Asthma Management: A Feasibility Study

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  • Additional Information
    • Contributors:
      Fingleton, J; McDonald, VM; Hardy, J; McLachlan, R; Gibson, PG; Pavord, ID; Agusti, A; Weatherall, M; Beasley, R; Anderson, A; Diputado, L; Eathorne, A; Gilchrist, J; Holliday, M; Kerse, K; Martindale, J; Shortt, N; Sparks, J; McDonald, V; Gibson, P; Nikolajevic‐Sarunac, J; Smith, A; Urroz, P
    • Publication Information:
      Wiley
    • Publication Date:
      2025
    • Collection:
      Oxford University Research Archive (ORA)
    • Abstract:
      Background and Objectives: Treatable trait‐based personalised medicine improves outcomes in severe asthma clinics. We assessed the feasibility of a randomised controlled trial (RCT) of protocolised treatable trait‐guided asthma management in patients not under a severe asthma clinic. Methods: Ten week single‐group cohort study. Participants had a doctor's diagnosis of asthma, Asthma Control Questionnaire‐5 (ACQ‐5) score > 1, and ≥ 1 exacerbation in the last year. Intervention: biomarker‐guided asthma medication according to a protocolised algorithm, targeting traits of type‐2 inflammation and airflow obstruction. Feasibility outcomes: recruitment rates, acceptability of intervention, willingness to enrol in an RCT, need for ‘extended’ trait assessment after 10 weeks, and estimation of trait prevalence. Results: Recruitment ceased with 29/50 participants after 14 months due to difficulties associated with COVID‐19. Recruitment rate: 29/118 (25%) of those invited to participate (95% CI 17 to 33). 24/26 (92%) participants found the intervention acceptable and were willing to participate in a future study. After 10 weeks, 65% remained not well controlled (ACQ‐5 > 1) and would have required the ‘extended’ assessment. Participants had a mean (SD) 4.8 (2.3) of 13 traits assessed. ACQ‐5 improved during the study by −1.0 (0.3 to 1.8) units, and post‐bronchodilator airflow limitation reduced from 59% of participants to 35%. 12/29 (41%) participants received continuous oral corticosteroids at some point during the study. Conclusion: Protocolised treatable trait management was acceptable to participants, associated with significant clinical benefit, and a full RCT appears feasible. Targeting type‐2 inflammation and airflow obstruction was insufficient to control asthma in the majority of patients, despite marked systemic corticosteroid exposure. Trial Registration: ACTRN12620000935932
    • Relation:
      https://doi.org/10.1111/resp.70016
    • Accession Number:
      10.1111/resp.70016
    • Online Access:
      https://doi.org/10.1111/resp.70016
      https://ora.ox.ac.uk/objects/uuid:f9da9cac-7182-4fd3-b389-aa766b1b9a8d
    • Rights:
      info:eu-repo/semantics/openAccess ; CC Attribution-NonCommercial-NoDerivatives (CC BY-NC-ND)
    • Accession Number:
      edsbas.1B6A919B