ArticleCureus2025
A Triple Threat: Immune Checkpoint Inhibitor-Induced Diabetic Ketoacidosis, Myocarditis, and Adrenal Insufficiency in a Patient With Metastatic Melanoma.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Immune checkpoint inhibitors (ICIs), such as ipilimumab and nivolumab, have revolutionized cancer therapy, particularly in advanced melanoma. By enhancing T-cell-mediated anti-tumor activity, these agents have significantly improved survival in metastatic disease. However, this immune activation can result in a range of immune-related adverse events (irAEs), which may affect virtually any organ system, sometimes with overlapping or atypical presentations. Endocrine irAEs, such as hypophysitis, thyroid dysfunction, and adrenalitis, are relatively well-described. Less commonly, ICIs can precipitate insulin-dependent diabetes mellitus or autoimmune myocarditis - both of which are rare but potentially life-threatening. These complications may present non-specifically, such as with fatigue or malaise, and are often under-recognized. This case highlights the importance of maintaining a high index of suspicion for multiple concurrent irAEs in patients on immunotherapy, even in the absence of overt clinical signs. Early recognition and prompt immunosuppressive therapy can significantly reduce morbidity and improve outcomes.
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Registered trials
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