Evidence map›Paper›PMID 40575214›Full record

ArticleCureus2025

Pembrolizumab-Induced Hypothyroidism and Diabetes Mellitus: A Rare Case Presentation Post-Treatment.

Jeevan Perera, Shubham Bhanot

Abstract readCase Reports
In one paragraph

Article in Cureus, 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. Article
  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

2 authors.

Jeevan PereraAcute Medicine, North Cumbria Integrated Care NHS foundation trust, Carlisle, GBR.
Shubham BhanotAcute Medicine, North Cumbria Integrated Care NHS foundation trust, Carlisle, GBR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pembrolizumab is a humanized monoclonal antibody that targets programmed death-1 (PD-1), a cell surface receptor expressed on activated T lymphocytes. By blocking the interaction between PD-1 and its ligands PD-L1 and PD-L2, pembrolizumab enhances T-cell-mediated immune responses against tumor cells. This immunotherapeutic strategy has shown significant clinical benefit in a range of malignancies, including metastatic melanoma, non-small cell lung cancer, and renal cell carcinoma. However, its mechanism of action can also disrupt immune self-tolerance, leading to immune-related adverse events (irAEs), particularly involving endocrine organs. These irAEs may manifest as autoimmune thyroiditis, hypophysitis, or, more rarely, insulin-dependent diabetes mellitus. In this case, the patient presented to a rural district general hospital with a several-week history of fatigue, polydipsia, and polyuria approximately two months after completing a one-year course of pembrolizumab for metastatic melanoma. Given the delayed and nonspecific symptom onset, diagnosis required a high degree of clinical suspicion. Laboratory investigations revealed severe hyperglycemia, suppressed C-peptide levels, and abnormal thyroid function tests. These findings were consistent with pembrolizumab-induced type 1 diabetes mellitus and hypothyroidism, both of which are recognized, though uncommon, endocrine irAEs.

Indexed as

drug-induced hypothyroidismendocrinopathyici-induced diabetes mellitusimmune checkpoint inhibitorsimmune checkpoint inhibitors induced endocrinopathiespembrolizumabpembrolizumab induced diabetes mellitus

Identifiers

PMID40575214
PMCPMC12199207

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.