Evidence map›Paper›PMID 38845140›Full record

ArticleESC heart failure2024

Predicting cardiovascular events with fluoropyrimidine chemotherapy using a standard cardiovascular risk calculator.

Aderonke Abiodun, Marianne Shawe-Taylor, Sara Tyebally, Emmanouil Bagkeris, Omotomilola Bajomo, Jessica Artico, Sarah Slater, Zahra Raisi-Estabragh, Nikolaos Diamantis, Charlotte Manisty

Abstract read
In one paragraph

Article in ESC heart failure, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

10 authors.

Aderonke AbiodunBarts Heart Centre, Barts Health NHS Trust, London, UK.ORCID 0000-0002-2304-3551
Marianne Shawe-TaylorBarts Heart Centre, Barts Health NHS Trust, London, UK.
Sara TyeballyBarts Heart Centre, Barts Health NHS Trust, London, UK.
Emmanouil BagkerisGreat Ormond Street Institute of Child Health, London, UK.
Omotomilola BajomoBarts Heart Centre, Barts Health NHS Trust, London, UK.
Jessica ArticoBarts Heart Centre, Barts Health NHS Trust, London, UK.
Sarah SlaterBarts Cancer Centre, Barts Health NHS Trust, London, UK.
Zahra Raisi-EstabraghBarts Heart Centre, Barts Health NHS Trust, London, UK.
Nikolaos DiamantisDepartment of Medical Oncology, Royal Free London NHS Foundation Trust, London, UK.
Charlotte ManistyBarts Heart Centre, Barts Health NHS Trust, London, UK.ORCID 0000-0003-0245-7090

Funding

British Heart FoundationNational Institute for Health and Care ResearchNIHR Barts Biomedical Research Centre, Queen Mary University of LondonUCLH Biomedical Research Centre
6 · The paper itself

Abstract

aimsFluoropyrimidine chemotherapy is important for treatment of many solid tumours but is associated with cardiotoxicity. The relationship of fluoropyrimidine-associated cardiotoxicity (FAC) with conventional cardiovascular (CV) risk factors is poorly understood, and standard cardiovascular risk scores are not validated in this context. METHODS AND

resultsSingle-centre retrospective study of patients treated with fluoropyrimidine chemotherapy using electronic health records for cardiovascular risk factors (and calculation of QRISK3 score), cancer treatment, and clinical outcomes. FAC was defined by cardiovascular events during or within 3 months of fluoropyrimidine treatment, and Cox regression was used to assess associations of CV risk and cancer treatment with FAC. One thousand eight hundred ninety-eight patients were included (45% male; median age 64 years), with median follow up 24.5 (11.5-48.3 months); 52.7% of patients were at moderate or high baseline CV risk (QRISK3 score >10%) Cardiovascular events occurred in 3.1% (59/1898)-most commonly angina (64.4%, 38/59) and atrial fibrillation (13.6%, 8/59), with 39% events during cycle one of treatment. In univariable analysis, QRISK3 score >20% was significantly associated with incident FAC (HR 2.25, 95% CI 1.11-4.93, P = 0.03). On multivariable analysis, beta-blocker use (HR 1.04, 95% CI 1.00-1.08, P = 0.04) and higher BMI (HR 2.33, 95% CI 1.04-5.19, P = 0.04) were independently associated with incident CV events. Thirty-two of the 59 patients with FAC were subsequently rechallenged with fluoropyrimidine chemotherapy, with repeat CV events in 6% (2/32). Incident FAC did not affect overall survival (P = 0.50).

conclusionsHigh BMI and use of beta-blockers are associated with risk of CV events during fluoropyrimidine chemotherapy. QRISK3 score may also play a role in identifying patients at high risk of CV events during fluoropyrimidine chemotherapy. Re-challenge with further fluoropyrimidine chemotherapy can be considered in patients following CV events during prior treatment.

Indexed as

Cardiovascular DiseasesAgedCardiotoxicityFemaleFluorouracilFollow-Up StudiesHeart Disease Risk FactorsHumansIncidenceMaleMiddle AgedNeoplasmsPyrimidinesRetrospective StudiesRisk AssessmentRisk FactorsFluorouracilPyrimidines5‐FUCapecitabineCardio oncologyCardiotoxicityFluoropyrimidinesQRISKRisk prediction

Identifiers

PMID38845140
PMCPMC11424348

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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.