AI-Driven Identification of High-Risk Patients with COPD for Biologic Therapy: Pathway Development Opportunities - European Medical Journal

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AI-Driven Identification of High-Risk Patients with COPD for Biologic Therapy: Pathway Development Opportunities

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Authors:
Anna Taylor , 1 Andrew Cushing , 1 Eve Walker , 1 David J. Lowe , 1,2 * Chris Carlin 1
  • 1. NHS Greater Glasgow and Clyde, UK
  • 2. University of Glasgow, UK
*Correspondence to [email protected]
Disclosure:

Taylor has received presentation fees from AstraZeneca; travel, accommodation, and registration support for the COPD Leadership Forum from AstraZeneca; and has joint working agreements with AstraZeneca and GlaxoSmithKline. Carlin has served on advisory boards for AstraZeneca, GlaxoSmithKline, Chiesi, and Sanofi Regeneron; received speaker fees for AstraZeneca, GlaxoSmithKline, Chiesi, and Sanofi Regeneron; travel and registration support from AstraZeneca to attend the European Respiratory Society (ERS) Congress and the British Thoracic Society (BTS) Conference; and has joint working agreements with AstraZeneca and GlaxoSmithKline. Cushing, Walker, and Lowe have joint working agreements with AstraZeneca and GlaxoSmithKline.

Citation:
Keywords:
AI, biologic therapy, COPD, pathway development, targeted identification.

Each article is made available under the terms of the Creative Commons Attribution-Non Commercial 4.0 License.

BACKGROUND

Biologic therapies targeting eosinophilic inflammation hold promise for COPD management. Realising their benefits will require effective patient identification and pathway development to improve access. AI-based risk prediction models offer a novel approach to stratify patients and optimise treatment delivery.

METHODS

Using de-identified routine clinical data from Glasgow Safe Haven, UK, the authors established a cohort of approximately 38,000 patients with a coded diagnosis of COPD.1 AI-based models were applied to the 2021 dataset to identify 3,639 patients at the highest risk of hospital admission within 6 months or mortality within 12 months. Among these, 382 patients had an eosinophil count >300 cells/μL in the preceding 12 months, despite using triple inhaler therapy, suggesting eligibility for biologic treatment.

RESULTS

The high-risk group’s adverse deprivation demographics mirrored the COPD burden in the wider population. Most biologic-eligible high-risk patients were aged >60 years and resided >5 km from central hospital sites where biologic therapies are typically initiated. However, a high proportion live <5 km from community vaccination hubs, presenting an opportunity to adapt treatment initiation locations. Based on RCT data, a projected reduction of 520 hospital admissions per year could be achieved in the authors’ organisation if biologic therapy were provided to this highest-risk cohort.

CONCLUSION

AI-driven risk prediction enables the targeted identification of patients with COPD who may benefit from biologic therapy. Model-derived insights can support pathway reconfiguration to improve access and equality, particularly via decentralised treatment initiation, facilitating timely intervention and better outcomes.

References
Taylor A et al. AI-driven identification of high-risk COPD patients for biologic therapy: pathway development opportunities. Abstract OA1190. ERS Congress, 27 September-1 October, 2025.

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