Evidence map›Paper›PMID 42828727›Full record

ReviewClinical and translational allergy2026

Efficacy of Biologics in Aspirin Exacerbated Respiratory Disease.

Jennifer K Priessnitz, Anastasia Hagopian, Alison J Patev, Joseph K Han, Kent K Lam

Abstract readReview
In one paragraph

Review in Clinical and translational allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jennifer K PriessnitzDivision of Internal Medicine, Macon & Joan Brock Virginia Health Sciences at Old Dominion University, Norfolk, Virginia, USA.ORCID https://orcid.org/0009-0003-3263-2897
Anastasia HagopianDepartment of Medicine, Eastern Virginia Medical School at Old Dominion University, Norfolk, Virginia, USA.ORCID https://orcid.org/0009-0009-6178-1377
Alison J PatevResearch and Infrastructure Service Enterprise, Macon & Joan Brock Virginia Health Sciences at Old Dominion University, Norfolk, Virginia, USA.ORCID https://orcid.org/0000-0001-8814-0259
Joseph K HanDivision of Allergy, Macon & Joan Brock Virginia Health Sciences at Old Dominion University, Norfolk, Virginia, USA.
Kent K LamDivision of Allergy, Macon & Joan Brock Virginia Health Sciences at Old Dominion University, Norfolk, Virginia, USA.ORCID https://orcid.org/0000-0002-1835-5390

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAspirin-exacerbated respiratory disease (AERD), also termed nonsteroidal anti-inflammatory drug exacerbated respiratory disease (NERD), is characterized by asthma, chronic rhinosinusitis with nasal polyposis, and hypersensitivity to cyclooxygenase-1 inhibitors, frequently resulting in severe, treatment-refractory airway disease. Biologic therapies targeting type 2 inflammation are increasingly used in AERD; though their relative efficacy remains incompletely defined.

methodsWe conducted a semi-systematic narrative review of biologic therapies in AERD, guided by established narrative review frameworks. PubMed/Medline, ScienceDirect, and ClinicalTrials.gov were searched for studies reporting clinical outcomes in AERD/NERD or clearly defined AERD/NERD subgroups. This review synthesizes current evidence and presents an evidence-informed clinical framework to support biologic selection in patients with AERD.

resultsEighteen studies identified, including randomized controlled trials, observational studies, and real-world studies. Across these studies, dupilumab was most consistently associated with improvements in both upper and lower airway outcomes. Anti-IL-5 and anti-IL-5Rα therapies reduced eosinophilia and asthma exacerbations, with variable sinonasal benefit. Omalizumab demonstrated efficacy in selected atopic phenotypes and in conjunction with aspirin therapy following desensitization. Emerging subgroup data suggests that Tezepelumab may reduce asthma exacerbations in AERD.

conclusionsCurrent evidence suggests biologic therapies provide meaningful benefit in AERD, although available evidence is limited by small sample sizes and heterogeneous designs. Prospective comparative studies are needed to inform optimal biologic selection and sequencing.

Indexed as

aspirin‐exacerbated respiratory diseasebiologicsbiologic therapynarrative reviewtype 2 inflammation

Identifiers

PMID42828727
PMCPMC13633742

What OpenQuestion holds

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Registered trials

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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.