Evidence map›Paper›PMID 41647338›Full record

ArticleESMO real world data and digital oncology2025

Cardiovascular toxicities in cancer patients treated with immune checkpoint inhibitors: multicenter study using natural language processing on Belgian hospital data.

D Delombaerde, C L Oeste, V Geldhof, L Croes, I Bassez, A Verbiest, L Tack, D Hens, C Franssen, P R Debruyne and 4 more

Abstract read
In one paragraph

Article in ESMO real world data and digital oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. 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

14 authors.

D DelombaerdeIntegrated Cancer Canter Ghent, Department of Medical Oncology, General Hospital AZ Maria Middelares, Ghent, Belgium.
C L OesteLynxCare, Leuven, Belgium.
V GeldhofDepartment of Oncology, General Hospital AZ Klina and General Hospital AZ Voorkempen, Antwerp, Belgium.
L CroesCenter for Oncological Research (CORE), University of Antwerp, Antwerp, Belgium.
I BassezLynxCare, Leuven, Belgium.
A VerbiestDepartment of Oncology, Multidisciplinary Oncological Center Antwerp, Antwerp University Hospital, Edegem, Belgium.
L TackKortrijk Cancer Center, General Hospital AZ Groeninge, Kortrijk, Belgium.
D HensLynxCare, Leuven, Belgium.
C FranssenDepartment of Cardiology, Antwerp University Hospital, Antwerp, Belgium.
P R DebruyneKortrijk Cancer Center, General Hospital AZ Groeninge, Kortrijk, Belgium.
H PrenenCenter for Oncological Research (CORE), University of Antwerp, Antwerp, Belgium.
M PeetersCenter for Oncological Research (CORE), University of Antwerp, Antwerp, Belgium.
J De SutterDepartment of Cardiology, General Hospital AZ Maria Middelares, Ghent, Belgium.
C VulstekeIntegrated Cancer Canter Ghent, Department of Medical Oncology, General Hospital AZ Maria Middelares, Ghent, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitor (ICI) use may be associated with diverse cardiovascular (CV) adverse events (AEs), but their baseline prevalence and incidence after ICI initiation are poorly known. We aimed to describe CV events using real-world hospital data from Belgian cancer patients. Materials and methods: Electronic health records (EHRs) from patients receiving at least one ICI between March 2017 and August 2022 at three Belgian hospitals were processed into an Observational Medical Outcomes Partnership Common Data Model warehouse. Structured data were enriched with unstructured data that were processed using a natural language processing (NLP) pipeline. We analyzed CV events from first ICI administration until last follow-up, identifying and validating the first detection of a CV event at the patient level. Results: We included 1571 patients (66% male, median age 67 years); CV events were detected in 196 (12.5%) patients [median (min-max) follow-up: 8 (0-63) months]. The CV AEs detected were heart failure (5.3%), atrial fibrillation (4.6%), myocardial infarction (2.0%), atrioventricular block (1.9%), myocarditis (1.2%), vasculitis (0.8%), pericarditis (0.4%), and Takotsubo cardiomyopathy (<0.3%). Median time (min-max) to onset ranged from 109 days (17-849 days) for myocarditis to 529 days (91-967 days) for Takotsubo cardiomyopathy. Conclusions: To our knowledge, this is the first study using a dataset enriched with NLP-processed EHRs that describes the frequency and onset time of CV events. CV event frequencies were higher than those reported in clinical trials, but similar to other real-world studies. However, we observed a later time to onset. Hence, clinicians should note that CV AEs can present in various ways and at any time during or after treatment.

Indexed as

cardiotoxicitycardiovascular adverse eventimmune checkpoint inhibitormyocarditisnatural language processingreal-world evidence

Identifiers

PMID41647338
PMCPMC12836667

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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.