Evidence map›Paper›PMID 40783691›Full record

ArticleBMC cancer2025

Immune checkpoint inhibitor-associated myocarditis and pericarditis: a pharmacovigilance study based on the FAERS database.

Guojing Yao, Yu Zhang, Haixia Zhang, Linlin Tang, Chuanhua Ding, Xueheng Zhou

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

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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

6 authors.

Guojing YaoDepartment of Pharmacy , Affiliated Hospital of Shandong Second Medical University, Weifang, 261031, Shandong, China. 1071505272@qq.com.
Yu ZhangDepartment of Pharmacy, Yantai Penglai People's Hospital, Yantai, 265600, Shandong, China.
Haixia ZhangDepartment of Pharmacy , Affiliated Hospital of Shandong Second Medical University, Weifang, 261031, Shandong, China.
Linlin TangDepartment of Pharmacy , Affiliated Hospital of Shandong Second Medical University, Weifang, 261031, Shandong, China.
Chuanhua DingDepartment of Pharmacy , Affiliated Hospital of Shandong Second Medical University, Weifang, 261031, Shandong, China.
Xueheng ZhouDepartment of Pharmacy , Affiliated Hospital of Shandong Second Medical University, Weifang, 261031, Shandong, China. 13963668866@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) are medications used in cancer immunotherapy. However, treatment with ICIs may lead to adverse effects, particularly myocarditis and pericarditis. This practical pharmacovigilance study investigates the relationship between ICIs and myocarditis and pericarditis using the FAERS (U.S. FDA Adverse Event Reporting System) database. RESEARCH DESIGN AND

methodsData on myocarditis and pericarditis related to ICIs were extracted from the FAERS database for the period from 2014Q1 to 2023Q4. Data mining was performed using the Bayesian Confidence Propagation Neural Network (BCPNN) and the Reporting Odds Ratio (ROR).

resultsA total of 1112 cases involving 1134 adverse event (AE) reports related to ICIs-associated noninfectious myocarditis/pericarditis (NM/P) were extracted from the FAERS database. After excluding reports with missing data, the primary reporters were physicians, consumers, and pharmacists, with the United States and Japan being the main reporting countries. The cases showed a greater percentage of males than females, with a median age of 67 years, a median weight of 65 kg, and a median onset time of 28 days. The signal strength of ICIs-associated NM/P, from highest to lowest, was as follows: Pembrolizumab (ROR: 12.32, 95% CI: 11.28-13.45, IC 025: 3.45) > Nivolumab (ROR: 11.23, 95% CI: 10.13-12.44, IC 025: 3.30) > Atezolizumab (ROR: 10.62, 95% CI: 8.67-13.02, IC 025: 3.10) > Ipilimumab (ROR: 10.25, 95% CI: 8.34-12.58, IC 025: 3.04) > Durvalumab (ROR: 9.25, 95% CI: 7.21-11.88, IC 025: 2.83).

conclusionThis study indicates that ICIs-associated NM/P significantly increases the mortality risk among cancer patients, particularly with the use of nivolumab and pembrolizumab. Strong signals for NM/P were observed with PD-1 inhibitors, pembrolizumab-based regimens, and the combination of nivolumab and ipilimumab. Additionally, a body weight of ≥ 75 kg and the use of nivolumab and ipilimumab may be potential significant risk factors for NM/P.

Indexed as

Immune Checkpoint InhibitorsMyocarditisNeoplasmsPericarditisAdultAdverse Drug Reaction Reporting SystemsAgedAged, 80 and overAntibodies, Monoclonal, HumanizedBayes TheoremDatabases, FactualFemaleHumansMaleMiddle AgedNivolumabAntibodies, Monoclonal, HumanizedImmune Checkpoint InhibitorsNivolumabData miningFDA adverse event reporting system (FAERS)Immune checkpoint inhibitors (ICIs)Myocarditis/pericarditisPharmacovigilance

Identifiers

PMID40783691
PMCPMC12335072

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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.