Evidence map›Paper›PMID 42780081›Full record

ArticleFrontiers in immunology2026

Immune checkpoint inhibitor-related thyroid dysfunction during treatment of lung cancer: a disproportionality analysis based on the FDA adverse event reporting system.

Yaqian Tan, Qi Song

Abstract read
In one paragraph

Article in Frontiers in immunology, 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

What it found

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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

2 authors.

Yaqian TanDepartment of Pharmacy, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China.
Qi SongDepartment of Pharmacy, Guangzhou Institute of Cancer Research, the Affiliated Cancer Hospital, Guangzhou Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitors (ICIs) have exhibited remarkable clinical benefits in the treatment of lung cancer, yet a large-scale pharmacovigilance investigation on ICI-related thyroid dysfunction (ICI-TD) remained limited. This study aimed to comprehensively analyze the demographic characteristics of ICI-TD in lung cancer patients and the pharmacovigilance signal patterns of the adverse events (AEs) using data from the Food and Drug Administration Adverse Event Reporting System (FAERS) database. Methods: All existing data ranging from January 1 Results: A total of 2,001 reports of ICI-TD during treatment of lung cancer were identified after data processing, involving 1,758 patients and 10 ICIs. In general, ICI-TD were mainly reported in male patients (n = 959, 54.55%) and patients aged ≥ 65 years (n = 856, 48.69%; median [lower quartile (Q1), upper quartile (Q3)] = 67 [60, 73]). After data cleaning, we found that reports from 752 patients had valid time-to-onset (TTO) values. The median TTO of ICI-TD was 42 days [Q1, Q3] = [14, 98], and ICI-TD was predominantly reported within 30 days after ICI administration (n = 323, 42.95% of all 752 patients). The vast majority of patients were reported as having serious reaction outcome (n = 1,690, 96.13%). Among all ICIs, nivolumab had the greatest number of ICI-TD reports (a = 655, 32.73% of all 2,001 reports, ROR Conclusions: The present study provided a comprehensive overview of the demographic features of patients and pharmacovigilance signal patterns of ICI-TD during the treatment of lung cancer. Our findings would offer a referential perspective for the clinical understanding of the pharmacovigilance signals of ICI-TD.

Indexed as

Adverse Drug Reaction Reporting SystemsImmune Checkpoint InhibitorsLung NeoplasmsThyroid DiseasesAdultAgedAged, 80 and overDatabases, FactualFemaleHumansMaleMiddle AgedPharmacovigilanceUnited StatesUnited States Food and Drug AdministrationImmune Checkpoint Inhibitorsadverse eventFAERSimmune checkpoint inhibitorspharmacovigilancethyroid dysfunction

Identifiers

PMID42780081
PMCPMC13597272

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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.