Evidence map›Paper›PMID 40280566›Full record

ArticleJournal for immunotherapy of cancer2025

Onset and progression of atherosclerosis in patients with melanoma treated with immune checkpoint inhibitors.

Daan C H van Dorst, Tom J J Uyl, Astrid A M Van der Veldt, Timy Andrawes, Arjen Joosse, Esther Oomen-De Hoop, Alexander Hj Danser, Ron H J Mathijssen, Daniel Bos, Jorie Versmissen

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

10 authors.

Daan C H van DorstDepartment of Medical Oncology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-6817-9156
Tom J J UylDepartment of Hospital Pharmacy, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands t.uyl@erasmusmc.nl.ORCID http://orcid.org/0009-0007-4789-9278
Astrid A M Van der VeldtDepartment of Medical Oncology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Timy AndrawesDepartment of Medical Oncology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Arjen JoosseDepartment of Medical Oncology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Esther Oomen-De HoopDepartment of Medical Oncology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Alexander Hj DanserDepartment of Vascular Medicine and Pharmacology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Ron H J MathijssenDepartment of Medical Oncology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-5667-5697
Daniel BosDepartment of Radiology and Nuclear Medicine, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Jorie VersmissenDepartment of Vascular Medicine and Pharmacology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) are effective anticancer agents but significantly increase cardiovascular risk. This could be due to its potential to induce or worsen atherosclerosis. We evaluated the onset and progression of atherosclerosis during ICI treatment in patients with melanoma and investigated risk factors for substantial (>10%/year) atherosclerotic plaque growth in five segments of the arterial tree.

methodsOnset and yearly progression of atherosclerosis were assessed in the aortic arch, descending thoracic aorta, abdominal aorta, left and right iliac arteries via CT scans performed prior to and 1 year (±3 months) after ICI therapy initiation in patients with melanoma in the adjuvant (resected melanoma) and advanced disease (irresectable stage III and stage IV) setting. The primary outcome was defined as yearly progression of maximal plaque thickness in each arterial segment. Secondary outcomes were changes in the number of plaques, incidence of arterial thrombosis (ATE), and factors associated with substantial plaque growth in the descending thoracic aorta.

resultsIn total, 244 patients were included. Plaque thickness increased significantly in all aortic segments, ranging from 3.0% to 8.0% per year (all p<0.001). In 75% of included patients, substantial plaque growth in ≥1 segment occurred. Number of plaques remained identical in 64-86% of arterial segments. Three (1.2%) developed ATE within 1 year after ICI initiation. ICI combination therapy demonstrated a trend towards increased risk of substantial plaque growth compared with monotherapy (OR 2.10 (95% CI, 0.95 to 4.66; p=0.068)), whereas antihypertensive drug usage was associated with a lower risk (OR 0.48 (95% CI, 0.24 to 0.95; p=0.036)).

conclusionThe majority of patients with melanoma experience substantial atherosclerotic plaque growth during ICI therapy. The number of plaques remained relatively stable, suggesting that ICIs could particularly affect pre-existing plaques.

Indexed as

AtherosclerosisImmune Checkpoint InhibitorsMelanomaAgedAged, 80 and overDisease ProgressionFemaleHumansMaleMiddle AgedPlaque, AtheroscleroticRisk FactorsImmune Checkpoint InhibitorsImmune Checkpoint InhibitorsMelanoma

Identifiers

PMID40280566
PMCPMC12035449

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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.