Evidence map›Paper›PMID 41027684›Full record

ArticleLupus science & medicine2025

Characterisation of systemic lupus erythematosus associated with immune checkpoint inhibitors: a pharmacovigilance study using FAERS database.

Lan Zhen, Hong Chen, Wuyuan Pan, Jianrong Song, Huan Yi, Hong Zhou

Abstract read
In one paragraph

Article in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Lan Zhen *Department of Gynecology Oncology, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, China.ORCID 0009-0003-4555-7099
Hong Chen *Department of Neurology, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Shengli Clinical College of Fujian Medical University, Fuzhou, Fujian, China.ORCID 0009-0002-0729-3144
Wuyuan PanDepartment of Gynecology Oncology, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, China.ORCID 0009-0006-8979-5066
Jianrong SongDepartment of Gynecology Oncology, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, China.ORCID 0009-0008-1193-645X
Huan YiDepartment of Gynecology Oncology, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, China banny_80p@msn.cn yi.huan@fjmu.edu.cn.ORCID 0009-0009-9209-916X
Hong ZhouDepartment of Pharmacy, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, China banny_80p@msn.cn yi.huan@fjmu.edu.cn.ORCID 0000-0002-4811-5064

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSLE associated with immune checkpoint inhibitors (ICIs) is rare, and a comprehensive profile of ICI-induced SLE remains poorly characterised. This study aimed to explore the potential association between ICIs and SLE and characterise clinical features.

methodsWe extracted adverse event reports of patients with cancer with SLE from the FAERS (US Food and Drug Administration Adverse Event Reporting System) database (Q1 2011-Q4 2024). A disproportionality analysis was conducted using the reporting OR (ROR) and the information component, with adjusted ROR calculated via logistic regression to control for confounders.

results146 066 ICI-related adverse events cases from patients with cancer were identified. Among these, 209 (median (IQR) age 63 (55.3-71.7) years; 106 (51%) female) cases of SLEs were reported. Our analysis detected significant positive signals for SLE associated with ICIs overall, particularly for anti-programmed cell death protein 1 (PD-1) and anti-programmed death-ligand 1 therapy. Eight positive signals of SLEs were identified, predominantly cutaneous lupus and SLE. The risk of ICI-related SLEs was significantly higher in females than in males. However, age and chemotherapy were not significant risk factors for the incidence of ICI-related SLEs. The risk was higher with anti-PD-1 therapy compared with other ICI therapies. Patients with lung cancer, melanoma or breast cancer appeared to be at higher risk. Most patients experienced serious outcomes, with a mortality rate of 4.31% (nine cases).

conclusionThis first pharmacovigilance study identified a significant association between ICI use and SLEs, suggesting ICIs may constitute a novel class of drug-induced SLE triggers. Personalised long-term safety monitoring for ICIs is warranted for high-risk patients (eg, females, anti-PD-1 recipients).

Indexed as

Immune Checkpoint InhibitorsLupus Erythematosus, SystemicNeoplasmsAdverse Drug Reaction Reporting SystemsAgedDatabases, FactualFemaleHumansMaleMiddle AgedPharmacovigilanceUnited StatesImmune Checkpoint InhibitorsEpidemiologyLupus Erythematosus, SystemicRisk FactorsSystemic Lupus Erythematosus

Identifiers

PMID41027684
PMCPMC12481352

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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.