Sinonasal Adverse Events of Immune Checkpoint Inhibitors: Pharmacovigilance Using FAERS

Document Type

Conference Proceeding

Publication Date

6-2026

Publication Title

Journal of Clinical Oncology

Abstract

Background: Immune checkpoint inhibitors (ICIs) are cancer therapies with diverse toxicities, known as immune-related adverse events (irAEs). Sinonasal irAEs have been described primarily in case reports, and their population-level characteristics remain poorly defined. To date, no statistical analysis of the FDA Adverse Events Reporting System Database (FAERS) has evaluated sinonasal adverse events (snAEs) associated with ICIs. Methods: We investigated snAEs associated with FDA-approved ICIs in FAERS between 1/1/2011 and 10/1/2025. ICIs were grouped by therapeutic target (PD-1, PD-L1, or CTLA-4). Analyses were conducted in R using Bioconductor package “faers”. Data were standardized using preferred term in the Medical Dictionary for Regulatory Activities and deduplicated based on concordance across drug, adverse event, and demographics. Disproportionality analysis used reporting odds ratio (RORs) in comparison with the overall FAERS database. We excluded adverse events with ,2 reports. The study was created and reviewed by the authors prior to implementation. Results: 17 million FAERS reports were identified, of which 2,476 ICI-associated reports included snAEs. Two rare events demonstrated significant disproportionality among PD-1 inhibitors: chronic eosinophilic rhinosinusitis (n=3; ROR 7.71, 95% CI 2.34–25.42) and nasal mucosal hypertrophy (n=2; ROR 8.67, 95% CI 1.99 - 37.73). In contrast, more frequently reported snAEs including sinusitis, rhinorrhea, nasal congestion, anosmia, nasal polyps, paranasal sinus inflammation, parosmia, and rhinitis, were not overreported (Overall ROR2.5 #1). Conclusions: In this large pharmacovigilance analysis snAEs were not broadly overreported after ICI therapy. Rare inflammatory phenotypes were disproportionately reported with PD-1 inhibition, suggesting an immune-mediated mechanism. Given the limitations of spontaneous reporting data and small event counts, these findings should be interpreted cautiously but highlight the need for increased clinical awareness and prospective studies to better characterize sinonasal immune-related toxicities.

Volume

44

Issue

16 Suppl

First Page

11146

Comments

American Society of Clinical Oncology (ASCO) Annual Meeting, May 29 - June 2, 2026, Chicago, IL

Last Page

11146

DOI

10.1200/JCO.2026.44.16_suppl.11146

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