Evidence map›Paper›PMID 40370338›Full record

ArticleLaryngoscope investigative otolaryngology2025

Association of Sinonasal Symptoms and Disease With Immune Checkpoint Inhibitor Therapy.

Jaynelle Gao, Ryan S Chung, Jason Chwa, Kevin Hur

Abstract read
In one paragraph

Article in Laryngoscope investigative otolaryngology, 2025. 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

4 authors.

Jaynelle GaoKeck School of Medicine University of Southern California California Los Angeles USA.ORCID https://orcid.org/0000-0002-1853-4460
Ryan S ChungKeck School of Medicine University of Southern California California Los Angeles USA.ORCID https://orcid.org/0000-0002-4732-9028
Jason ChwaKeck School of Medicine University of Southern California California Los Angeles USA.
Kevin HurCaruso Department of Otolaryngology-Head and Neck Surgery Keck School of Medicine of University of Southern California California Los Angeles USA.ORCID https://orcid.org/0000-0001-7016-4375

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitors (ICIs) are widely used for cancer therapy and are associated with immune-related adverse events (irAEs) in various organ systems. However, data on sinonasal irAEs remain limited. This study investigates the association between ICI therapy and sinonasal conditions, including chronic rhinosinusitis (CRS) and nasal polyps, using a national health database. Methods: This retrospective cohort study utilized the TriNetX US Network to analyze adults diagnosed with malignant neoplasms for which ICIs are an accepted treatment option. Patients treated with FDA-approved ICIs (pembrolizumab, nivolumab, cemiplimab, atezolizumab, durvalumab, avelumab, or ipilimumab) were compared to those not receiving ICIs. Exclusion criteria included sinonasal neoplasms and prior sinus surgery. Propensity score matching on age, race, sex, and asthma diagnosis was performed. Outcomes included first-time diagnoses of CRS, nasal polyps, and cardinal symptoms of CRS. Subgroup analyses by ICI mechanism of action and a post hoc analysis of all-cause mortality were conducted. Results: ICI therapy was associated with a decreased likelihood of CRS diagnosis (OR 0.90, 95% CI 0.85-0.96), nasal polyp diagnosis (OR 0.65, 95% CI 0.51-0.83), and facial pain (OR 0.74, 95% CI 0.56-0.99). Conversely, patients receiving ICIs had an increased likelihood of anosmia/parosmia or parageusia (OR 1.86, 95% CI 1.68-2.07), and rhinorrhea (OR 1.16, 95% CI 1.10-1.22). Subgroup analyses supported these findings across different ICI categories. Risk of mortality was higher among ICI-treated patients (HR 4.09, 95% CI 4.02-4.16). Conclusion: This is the first propensity-matched study to evaluate the relationship between ICI therapy and sinonasal conditions, revealing a decreased risk of CRS and nasal polyps in patients undergoing ICI therapy. Future studies are needed to explore the clinical significance and mechanism of ICI-related sinonasal symptoms. Level of Evidence: 3.

Indexed as

chronic rhinosinusitisimmune‐related adverse eventsnasal polypspembrolizumab

Identifiers

PMID40370338
PMCPMC12076599

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.