Evidence map›Paper›PMID 41282287›Full record

ArticleFrontiers in endocrinology2025

Immune checkpoint inhibitor-induced diabetes can potentially be effectively treated with infliximab: a case report of two patients.

Noam Savion Gaiger, Michael E Hurwitz, Navid Hafez, Harriet M Kluger, Kevan C Herold, Ana Luisa Perdigoto

Abstract readCase Reports
In one paragraph

Article in Frontiers in endocrinology, 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. Article
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.

Noam Savion GaigerMedical Oncology, Yale School of Medicine, New Haven, CT, United States.
Michael E HurwitzMedical Oncology, Yale School of Medicine, New Haven, CT, United States.
Navid HafezHematology Oncology, Cedars Sinai, Los Angeles, CA, United States.
Harriet M KlugerMedical Oncology, Yale School of Medicine, New Haven, CT, United States.
Kevan C HeroldDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, United States.
Ana Luisa PerdigotoDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, United States.

Funding

Elucidating mechanisms of checkpoint inhibitor-induced diabetesK08CA282972 · NCI · YALE UNIVERSITY · PI Ana Luisa Jordao Perdigoto · 2023 to 2026
$694k
NCI NIH HHS K08 CA282972
6 · The paper itself

Abstract

Immune checkpoint inhibitor-induced diabetes is a potentially severe and life-threatening complication of immune checkpoint inhibitor therapy in patients with advanced malignancies. It is typically an irreversible complication due to the complete destruction of pancreatic beta cells that requires ongoing insulin treatment, and patients often exhibit labile diabetes. Inflammatory cytokines, including TNF-α, are thought to play a role in the development of this form of diabetes, as they do in spontaneous autoimmune diabetes. TNF-α has also been implicated in the development of other immune-related adverse events caused by immunotherapy, and infliximab, a TNF-α monoclonal antibody, has shown efficacy in several of these complications. We tested whether infliximab could preserve beta-cell function in immune checkpoint inhibitor-induced diabetes. We present two cases in which infliximab treatment appeared to halt beta-cell destruction, as evidenced by maintenance of C-peptide levels, as well as improved clinical outcomes in terms of diabetes control.

Indexed as

Diabetes MellitusImmune Checkpoint InhibitorsInfliximabHumansInsulin-Secreting CellsMiddle AgedImmune Checkpoint InhibitorsInfliximabdiabetes mellitusimmune checkpoint inhibitorsimmune related adverse eventsinfliximabTNF-α

Identifiers

PMID41282287
PMCPMC12634352

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.