Evidence map›Paper›PMID 42496605›Full record

ArticleTechnology in cancer research & treatment

Pharmacovigilance Evaluation of Noninfectious Myocarditis and Pericarditis in Immune Checkpoint Inhibitor Recipients Using FAERS.

Xiangtian Xiao, Hongyan Su, Chengning Ma, Yamin Shu, Yiling Ding, Pingping Xu, Wenting Zhang

Abstract read
In one paragraph

Article in Technology in cancer research & treatment. 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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0citing papers in PubMed
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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

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

7 authors.

Xiangtian XiaoDepartment of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hongyan SuDepartment of Pharmacy, The People's Hospital of Lincang, Lincang, China.
Chengning MaFirst Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Yamin ShuDepartment of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yiling DingDepartment of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Pingping XuDepartment of Colorectal Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Wenting ZhangDepartment of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID 0000-0002-1833-8152

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IntroductionImmune-related adverse events (irAEs) pose considerable challenges to the clinical application of immune-checkpoint inhibitors (ICIs). Noninfectious myocarditis/pericarditis is a class of ICI-associated adverse events with a high fatality rate in real-world settings. This study aimed to comprehensively assess noninfectious myocarditis/pericarditis adverse events associated with ICIs.MethodsReports of ICI-related noninfectious myocarditis/pericarditis AEs were extracted from the FDA Adverse Event Reporting System (FAERS) database. Disproportionality analysis was performed using the reporting odds ratio (ROR). Serious and non-serious outcomes of noninfectious myocarditis/pericarditis cases were compared using the Mann-Whitney U test or chi-squared test, and clinical priority was assigned to signals by scoring five features on a 0- to 10-point scale. Factors associated with reporting were explored based on stratified analyses.ResultsReports of noninfectious myocarditis/pericarditis AEs accounted for 1.67% of all ICI AE reports during the study period in the FAERS database. The median age of the patients was 70 years (interquartile range [IQR] 62-76), and 94.66% of reports had serious outcomes. Eight categories of noninfectious myocarditis/pericarditis AEs with positive RORs were identified. Noninfectious myocarditis/pericarditis AEs treated with ICIs were more frequently reported in male and older patients. Of note, 2, 3 and 3 AEs were identified as strong, moderate, and weak clinical priorities, respectively. The median time to onset (TTO) of strong, moderate and weak AEs for ICI treatments was 25 (IQR 14-61), 56 (IQR 24.50-116.25) and 124 (IQR 29-301) days, respectively. All disproportionality signals showed early-failure patterns, with the hazard of AE reporting decreasing over time.ConclusionsThis study suggests a significant disproportionality signal between ICIs and noninfectious myocarditis/pericarditis AEs, and the findings provide supporting evidence for clinicians in managing these AEs.

Indexed as

Adverse Drug Reaction Reporting SystemsDrug-Related Side Effects and Adverse ReactionsImmune Checkpoint InhibitorsMyocarditisNeoplasmsPericarditisPharmacovigilanceAgedDatabases, FactualFemaleHumansMaleMiddle AgedImmune Checkpoint Inhibitorsdisproportionality analysisFAERSimmune checkpoint inhibitorsmyocarditis/pericarditispharmacovigilance

Identifiers

PMID42496605
PMCPMC13400914

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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.