Evidence map›Paper›PMID 40439712›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2025

Artificial intelligence-enabled opportunistic identification of immune checkpoint inhibitor-related adverse events using [

Clemens P Spielvogel, Aleksa Lazarevic, Lucia Zisser, David Haberl, Christophoros Eseroglou, Lucian Beer, Marcus Hacker, Raffaella Calabretta

Abstract read
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 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. Review
  2. Review
  3. Synthetic imaging for research and education in nuclear medicine: Who's afraid of the black box?European journal of nuclear medicine and molecular imaging · 2025
    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

8 authors.

Clemens P SpielvogelDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Aleksa LazarevicDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Lucia ZisserDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
David HaberlDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Christophoros EseroglouDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Lucian BeerDivision of General and Pediatric Radiology, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria.
Marcus HackerDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Raffaella CalabrettaDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria. raffaella.calabretta@meduniwien.ac.at.ORCID 0000-0002-8018-3884

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmune checkpoint inhibitors (ICI) have transformed cancer therapy, improving outcomes in malignancies like lung cancer, melanoma, and lymphoma by targeting PD-1, PD-L1, and CTLA-4 to enhance T cell-mediated tumor destruction. However, ICI often induce immune-related adverse events (irAEs) across multiple organs. [18F]FDG PET/CT is a valuable tool for assessing immune activation, but whole-organ inflammation evaluation remains time-consuming and prone to variability. This study investigates AI-driven organ-level [18F]FDG PET/CT uptake changes pre- and post-ICI therapy to opportunistically detect irAEs.

methodsA total of 64 patients with lung cancer, melanoma, or lymphoma who underwent [18F]FDG PET/CT before and after ICI therapy were included. Automated delineation of anatomical structures was performed using an artificial intelligence approach involving multiple subsequently applied deep learning models. SUVmax and SUVmean were quantified for irAE-related organs (thyroid, myocardium, pancreas, liver, bone, spleen, and adrenal glands) after automated tumor lesion removal. Statistical analysis identified uptake changes linked to clinically observed inflammation-related adverse events.

resultsAmong 64 patients (mean scan interval 4.5 months), thyroid uptake increased post-ICI (ΔSUVmax=0.44, p = 0.04; ΔSUVmean=0.22, p = 0.08). Increased uptake occurred in 55% (SUVmax) and 53% (SUVmean) of patients. Thyroid-related adverse events were more frequent in those with increased uptake (29% vs. 3%, p = 0.008), with uptake increase being the most pronounced in the cases of hypothyroidism (p = 0.002 for SUVmax, p = 0.03 for SUVmean). Myocardial, pancreatic, and hepatic uptake increased but without statistical significance (p > 0.05).

conclusionAI-enabled opportunistic [18F]FDG PET/CT screening effectively detects thyroid-related irAEs, particularly hypothyroidism, through uptake quantification. This approach offers a promising biomarker for early irAE detection, enhancing patient management and immunotherapy optimization.

Indexed as

Artificial IntelligenceFluorodeoxyglucose F18Immune Checkpoint InhibitorsPositron Emission Tomography Computed TomographyAgedFemaleHumansMaleMiddle AgedFluorodeoxyglucose F18Immune Checkpoint InhibitorsAdverse eventsArtificial intelligenceFDGImmune checkpoint inhibitors

Identifiers

PMID40439712
PMCPMC12589324

What OpenQuestion 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 OpenQuestion graph.