Evidence map›Paper›PMID 40962844›Full record

ArticleBritish journal of cancer2025

CA125 and age-based models for ovarian cancer detection in primary care: a population-based external validation study.

Kirsten D Arendse, Fiona M Walter, Gary Abel, Brian Rous, Willie Hamilton, Emma J Crosbie, Garth Funston

Abstract readValidation Study
In one paragraph

Article in British journal 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
  2. Review
  3. Article
  4. Article
  5. Is now the time to rethink risk thresholds in cancer referral guidelines?The British journal of general practice : the journal of the Royal College of General Practitioners · 2025
    Article
  6. 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

7 authors.

Kirsten D ArendseWolfson Institute of Population Health, Queen Mary University of London Barts and The London School of Medicine and Dentistry, London, United Kingdom.ORCID http://orcid.org/0000-0001-9046-1086
Fiona M WalterWolfson Institute of Population Health, Queen Mary University of London Barts and The London School of Medicine and Dentistry, London, United Kingdom.
Gary AbelUniversity of Exeter Medical School, University of Exeter, Exeter, United Kingdom.ORCID http://orcid.org/0000-0003-2231-5161
Brian RousCambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
Willie HamiltonUniversity of Exeter Medical School, University of Exeter, Exeter, United Kingdom.
Emma J CrosbieGynaecological Oncology Research Group, Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom.ORCID http://orcid.org/0000-0003-0284-8630
Garth FunstonWolfson Institute of Population Health, Queen Mary University of London Barts and The London School of Medicine and Dentistry, London, United Kingdom. g.funston@qmul.ac.uk.ORCID http://orcid.org/0000-0002-4156-6401

Funding

Cancer Research UK (CRUK) 8640/A23385DH | National Institute for Health Research (NIHR) NIHR203308DH | National Institute for Health Research (NIHR) NIHR300650DH | National Institute for Health Research (NIHR) PR-PRU-1217-21601
6 · The paper itself

Abstract

backgroundCancer antigen-125 (CA125) is widely used to investigate symptoms of possible ovarian cancer (OC) in primary care. However, OC risk varies with age and CA125 level. We externally validated the Ovatools models, which provide CA125- and age-specific OC risk.

methodsThe performance of Ovatools in predicting OC diagnosis within 12 months of primary care CA125 was examined using English healthcare data for women <50 and ≥50 years. Discrimination and calibration were examined, accuracy was calculated at varying risk thresholds and compared to CA125 ≥ 35U/ml. We estimated OCs missed/detected by Ovatools in hypothetical diagnostic pathways, including a two-threshold pathway where moderate risk (1-2.9%) triggered primary care ultrasound, and higher risk (≥3%) triggered urgent cancer referral.

results342,278 women were included, 0.63% had OC. The AUC was 0.95 in women ≥50 and 0.89 in women <50. When sensitivity/specificity were matched to CA125 ≥ 35U/ml, Ovatools showed marginally improved performance across other accuracy metrics in women ≥50 years. In a two-threshold pathway (≥50 years), 18.3% identified for urgent referral and 1% identified for ultrasound had OC. DISCUSSION: Ovatools performed well on external validation. Ovatools could be used to support informed decision-making and to triage women for further investigation based on cancer risk.

Indexed as

CA-125 AntigenMembrane ProteinsOvarian NeoplasmsAdultAgedAged, 80 and overAge FactorsEarly Detection of CancerFemaleHumansMiddle AgedPrimary Health CareCA-125 AntigenMembrane ProteinsMUC16 protein, human

Identifiers

PMID40962844
PMCPMC12603205

What Socratic 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 Socratic graph.