Evidence map›Paper›PMID 42662812›Full record

ArticleThe World Allergy Organization journal2026

Prevalence and cost implications of broadening asthma biologic eligibility criteria.

Freda Yang, Benjamin P Geisler, Grainne d'Ancona, Bohee Lee, David J Jackson, Chloe I Bloom

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Article in The World Allergy Organization journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Freda YangNational Heart and Lung Institute, Imperial College London, London, UK.
Benjamin P GeislerDepartment of Health Management and Health Economics, University of Oslo, Oslo, Norway.
Grainne d'AnconaGuy's & Brompton Asthma Network, Guy's Hospital, Guy's and St Thomas' NHS Foundation Trust Hospital, London, UK.
Bohee LeeNational Heart and Lung Institute, Imperial College London, London, UK.
David J JacksonGuy's & Brompton Asthma Network, Guy's Hospital, Guy's and St Thomas' NHS Foundation Trust Hospital, London, UK.
Chloe I BloomNational Heart and Lung Institute, Imperial College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rationale: Eligibility for biologic therapy in severe asthma varies internationally because government-funded schemes apply stricter criteria than pivotal trials. While relaxing eligibility thresholds may expand access, the effects on prevalence and healthcare costs remain uncertain. Objective: To quantify how alternative biologic eligibility criteria affect prevalence, clinical characteristics, and budget impact in adults with asthma. Methods: We studied adults with active asthma (2004-2021) using nationally representative primary care and hospital records. Biologic eligibility was assessed yearly using asthma severity (inhaled corticosteroid dose, additional controllers, rescue therapy) and exacerbations (oral corticosteroid prescriptions, emergency visits and hospitalisations). We assessed prevalence using United Kingdom (UK) criteria (severe asthma, ≥3 exacerbations), Global criteria (severe asthma, ≥1 or ≥2 exacerbations) and RCT criteria (moderate asthma, ≥1 or ≥2 exacerbations). Anti-IL-5/5Rα eligibility was evaluated using blood eosinophil counts. Budget impact was modelled over 5 years. Results: Among 1,306,307 asthma patients, 7.2% had severe asthma. Under UK criteria, 19,093 patients were biologic-eligible (20.4% of severe asthma; 1.5% of all asthma). Global criteria increased eligibility to 2.4% (≥2 exacerbations) to 4.3% (≥1 exacerbation), while RCT criteria expanded eligibility to 4.7% (≥2 exacerbations) and 9% (≥1 exacerbation). Among patients with eosinophil data, 38-45% met anti-IL-5/5Rα criteria. UK-eligible patients had higher prevalence of lower respiratory tract infections, pneumonia, and bronchiectasis. Five-year costs were £261 M under UK criteria, £436-767 M under Global criteria, and £878M-1.6B under RCT criteria. Conclusion: Only one-fifth of patients with severe asthma met UK biologic eligibility. Global criteria tripled eligibility and RCT criteria increased it six-fold, with substantial budget implications.

Indexed as

Anti-IL5Anti-TSLPBiologicExacerbationsSevere asthma

Identifiers

PMID42662812
PMCPMC13520886

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.