Evidence map›Paper›PMID 41912473›Full record

ArticleCancer medicine2026

A Disproportionality Analysis of Immune Checkpoint Inhibitors in Combination With Platinum-Based Agents Using the FDA Adverse Event Reporting System Database.

Boyi Liu, Wenchao Zhang, Ruizhe Huang, Dinwen Liu, Jiaxing Liu, Ao Han, Yike Li, Danna Chen

Abstract read
In one paragraph

Article in Cancer medicine, 2026. 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
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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

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

8 authors.

Boyi LiuThe First Clinical College, Changsha Medical University, Changsha, China.ORCID https://orcid.org/0009-0005-9184-4472
Wenchao ZhangThe First Clinical College, Changsha Medical University, Changsha, China.
Ruizhe HuangThe First Clinical College, Changsha Medical University, Changsha, China.ORCID https://orcid.org/0009-0005-6686-3452
Dinwen LiuThe First Clinical College, Changsha Medical University, Changsha, China.
Jiaxing LiuInstitute of Cytology and Genetics, Basic Medical School, University of South China, Hengyang, China.
Ao HanThe First Clinical College, Changsha Medical University, Changsha, China.
Yike LiChangsha Hospital for Maternal & Child Health Care, Changsha, China.
Danna ChenDepartment of Basic Medical Sciences, Changsha Medical University, Changsha, Hunan, China.

Funding

Changsha Outstanding Youth Innovation Talent Development Program kq2106074Hunan Provincial Department of Education Fund Project 23A0667National Undergraduate Innovation and Entrepreneurship Training Program 2024 (Letter No. 13 [2024] from the Department of Higher Education) S202410823011Natural Science Founda- tion of Hunan Province (2026JJ81233)The "14th Five-Year Plan" Applied Characteristic Discipline of Hunan ProvinceThe 2024 Hunan Provincial Student Innovation and Entrepreneurship Training Program Project, Xiang- jiaotong [2024] 191 - General Project - 5276
6 · The paper itself

Abstract

objectiveImmune checkpoint inhibitors (ICIs) combined with platinum-based compounds are commonly used in the treatment of certain malignant tumors. This study aims to analyze adverse events (AEs) associated with the combination therapy of ICIs and platinum-based compounds by using the FAERS database.

methodsThis study retrieved relevant adverse event (AE) data from the FAERS database (2008-2024) and conducted a retrospective analysis of the collected AEs. Multiple disproportionality analysis algorithms were employed, including the Reporting Odds Ratio (ROR), Proportional Reporting Ratio (PRR), Bayesian Confidence Propagation Neural Network (BCPNN), and Multi-item Gamma Poisson Shrinker (MGPS).

resultsAnalysis of 28,585 reports identified 27 significant SOC-level signals, strongest for hematological (ROR = 6.3), endocrine (ROR = 14.3), and hepatobiliary disorders (ROR = 4.49). Key PTs included malignant neoplasm progression (ROR = 16), febrile neutropenia (ROR = 15.31), and myocarditis (ROR = 16.3). 45.5% of AEs occurred within 1 month (median onset: 38 days). Combination therapy showed lower rates vs. monotherapy for malignancy progression and nephrotoxicity, but higher neurotoxicity (628 neuropathy cases).

conclusionThe combination exhibits distinct early-onset toxicities (early-onset hematological/endocrine/hepatic) and novel risks (neuropathy/myocarditis/leukemia), necessitating enhanced initial monitoring and subgroup-specific management.

Indexed as

Adverse Drug Reaction Reporting SystemsAntineoplastic Combined Chemotherapy ProtocolsImmune Checkpoint InhibitorsNeoplasmsPlatinum CompoundsBayes TheoremDatabases, FactualHumansRetrospective StudiesUnited StatesUnited States Food and Drug AdministrationImmune Checkpoint InhibitorsPlatinum Compoundsdisproportionality analysisFAERSimmune checkpoint inhibitorsplatinum‐based agents

Identifiers

PMID41912473
PMCPMC13140968

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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.