Evidence map›Paper›PMID 40202479›Full record

ArticleJACC. CardioOncology2025

Fluoropyrimidine Chemotherapy and the Risk of Death and Cardiovascular Events in Patients With Gastrointestinal Cancer.

Aderonke T Abiodun, Chengsheng Ju, Catherine A Welch, Jennifer Lai, Freya Tyrer, Pinkie Chambers, Lizz Paley, Sally Vernon, NICOR Collaborative, John Deanfield and 9 more

Abstract read
In one paragraph

Article in JACC. CardioOncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Fluoropyrimidine-induced cardiotoxicity: outcomes and safety of chemotherapy reintroduction in a retrospective cohort study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
  3. Article
  4. 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

19 authors.

Aderonke T AbiodunInstitute of Cardiovascular Science, University College London, United Kingdom; Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom; National Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom.
Chengsheng JuInstitute of Cardiovascular Science, University College London, United Kingdom; National Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom; Research Department of Practice and Policy, School of Pharmacy, University College London, United Kingdom.
Catherine A WelchNational Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom; Department of Population Health Sciences, University of Leicester, Leicester, United Kingdom.
Jennifer LaiNational Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom.
Freya TyrerNational Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom; Department of Population Health Sciences, University of Leicester, Leicester, United Kingdom.
Pinkie ChambersResearch Department of Practice and Policy, School of Pharmacy, University College London, United Kingdom; Cancer Division, University College London Hospitals NHS Foundation Trust, London, United Kingdom; Centre for Medicines Optimization Research and Education, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
Lizz PaleyNational Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom.
Sally VernonNational Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom.
NICOR Collaborative
John DeanfieldInstitute of Cardiovascular Science, University College London, United Kingdom; National Institute of Cardiovascular Outcomes Research, NHS Arden and Greater East Midlands Commissioning Support Unit, Leicester, United Kingdom.
Mark de BelderNational Institute of Cardiovascular Outcomes Research, NHS Arden and Greater East Midlands Commissioning Support Unit, Leicester, United Kingdom.
Mark J RutherfordDepartment of Population Health Sciences, University of Leicester, Leicester, United Kingdom.
Paul C LambertDepartment of Population Health Sciences, University of Leicester, Leicester, United Kingdom; Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
Sarah SlaterBarts Cancer Centre, Barts Health NHS Trust, London, United Kingdom.
Kai-Keen ShiuCancer Division, University College London Hospitals NHS Foundation Trust, London, United Kingdom; Cancer Institute, University College London, London, United Kingdom.
Li WeiResearch Department of Practice and Policy, School of Pharmacy, University College London, United Kingdom; Centre for Medicines Optimization Research and Education, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
Michael D PeakeDepartment of Respiratory Medicine, University of Leicester, Glenfield Hospital, Leicester, United Kingdom; Cancer Research UK, London, England.
David AdlamDepartment of Cardiovascular Sciences and NIHR Leicester Biomedical Research Centre, University of Leicester, Glenfield Hospital, Leicester, United Kingdom.
Charlotte ManistyInstitute of Cardiovascular Science, University College London, United Kingdom; Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom; National Disease Registration Service, NHS England, Wellington Place, Leeds, United Kingdom. Electronic address: c.manisty@ucl.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFluoropyrimidine chemotherapy is administered first-line for many gastrointestinal cancers. However, patients with cardiovascular disease commonly receive alternative treatment due to cardiotoxicity concerns.

objectivesThis study sought to assess the risks of all-cause mortality and acute cardiovascular events with fluoropyrimidine treatment.

methodsWe conducted an observational cohort study applying a target trial emulation framework to linked national cancer, cardiac, and hospitalization registry data from the Virtual Cardio-Oncology Research Initiative. Adults diagnosed with tumors eligible for fluoropyrimidine-based chemotherapy as first-line therapy were included. All-cause mortality and a composite of hospitalization for acute cardiovascular events (acute coronary syndrome, heart failure, cardiac arrhythmia, cardiac intervention, cardiac arrest, and cardiac death) were compared in patients treated with fluoropyrimidine-based chemotherapy vs alternative management. Adjusted, weighted pooled logistic regression models were used to estimate the 1-year risk difference (RD).

resultsAmong 103,110 patients (mean age 69.7 years, 59% male), the absolute risk of death at 1 year was significantly lower in fluoropyrimidine-treated patients (RD: -7.7%; 95% CI: -8.7% to -6.7%) with a small increased risk of acute cardiovascular events (RD: 0.9%; 95% CI: 0.0% to 1.9%). This was primarily due to arrhythmias (RD: 0.8%; 95% CI: 0.1% to 1.6%) and cardiac arrest (RD: 0.3%; 95% CI: 0.1% to 0.5%), with no increased risk of acute coronary syndromes including in the subgroup of patients with pre-existing coronary artery disease.

conclusionsThe markedly improved overall survival with fluoropyrimidines in patients with gastrointestinal cancer significantly outweighs the small risk of cardiac arrhythmia and arrest. Oncologists should take this into consideration for decision making to avoid undue clinical conservatism, particularly in patients with cardiovascular disease.

Indexed as

5-fluorouracilarrhythmiacapecitabinecardiotoxicitygastrointestinal canceroutcomesrisk predictionsudden deathtarget trial emulationvasospasm

Identifiers

PMID40202479
PMCPMC12228134

What OpenQuestion holds

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Registered trials

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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.