Evidence map›Paper›PMID 39925806›Full record

ArticleFrontiers in immunology2025

Immune checkpoint inhibitor-induced diabetes mellitus: clinical characteristics and risk factors.

Mei Zhan, Qinran Long, Jinhan He, Litao Huang, Bin Wu, Haixia Xu, Li Mo, Ting Xu

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Diabetes and cancer: glucose control impact on survival and tumor outcomes.Reviews in endocrine & metabolic disorders · 2026
    Review
  3. 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

8 authors.

Mei ZhanDepartment of Pharmacy, West China Hospital, Sichuan University, Chengdu, China.
Qinran LongDepartment of Pharmacy, West China Hospital, Sichuan University, Chengdu, China.
Jinhan HeDepartment of Pharmacy, West China Hospital, Sichuan University, Chengdu, China.
Litao HuangDepartment of Clinical Research Management, West China Hospital, Sichuan University, Chengdu, China.
Bin WuDepartment of Pharmacy, West China Hospital, Sichuan University, Chengdu, China.
Haixia XuDepartment of Pharmacy, Institute of Metabolic Diseases and Pharmacotherapy, West China Hospital, Sichuan University, Chengdu, China.
Li MoCenter of Gerontology and Geriatrics, West China Hospital, Sichuan University, Chengdu, China.
Ting XuDepartment of Pharmacy, West China Hospital, Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Emerging evidence indicates that immune checkpoint inhibitor-induced diabetes mellitus (ICI-DM) might be more common than initially reported, and more different clinical pictures associated with ICI-DM were described. Objective: The aim of our study was to identify the clinical characteristics and possible predictive factors of ICI-DM. Methods: We conducted a retrospective review of patients who received immune checkpoint inhibitors (ICI) at West China Hospital, Sichuan University until June 2023. Patients were reviewed at death or on 7 May 2024. We applied logistic regression to study the associations between clinical characteristics and ICI-DM. Results: Our study included 8,199 participants who received ICI between October 2014 and June 2023. Among them, 1,077 patients (13.14%) developed ICI-DM according to diagnostic criteria based on guidelines. By excluding patients influenced by glucocorticoids or immunosuppressants, ICI-DM was observed in 713 of 8,199 (8.70%) patients. In all patients, hypertension, hyperlipidemia, using glucocorticoids or immunosuppressants, lung cancer, and using more than one pathway of ICI were associated with a higher risk of ICI-DM. However, the risk factors for ICI-DM in patients without the influence of glucocorticoids or immunosuppressants were only hypertension, hyperlipidemia, and pancreatic lesions. In all patients and those patients without the influence of glucocorticoids and immunosuppressants, hypertension and hyperlipidemia may increase the risk for ICI-DM. Conclusions: This large, real-world cohort demonstrates that the incidence of ICI-DM may be underestimated in previous literature. Blood glucose monitoring is needed in patients receiving ICI therapy. Clinical trial registration: https://www.chictr.org.cn, identifier ChiCTR2300075974.

Indexed as

Diabetes MellitusImmune Checkpoint InhibitorsNeoplasmsAdultAgedAged, 80 and overChinaCohort StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsImmune Checkpoint Inhibitorscancerdiabetes mellitusimmune checkpoint inhibitorsimmune-related adverse eventsimmunotherapy

Identifiers

PMID39925806
PMCPMC11802519

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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.