Evidence map›Paper›PMID 42288686›Full record

ArticleBritish journal of cancer2026

Can ovarian cancer screening work? A secondary analysis of the UK collaborative trial of ovarian cancer screening.

Jane M Lange, Ishfaq Ahmad, Isabel J Dengos, Andy Ryan, Sophia Apostolidou, Aleksandra Gentry-Maharaj, Shannon Holloway, Marc D Ryser, Usha Menon, Ruth Etzioni

Abstract read
In one paragraph

Article in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jane M LangeCancer Early Detection Advanced Research Center, Oregon Health and Science University, Oregon, OR, USA. langeja@ohsu.edu.ORCID http://orcid.org/0000-0002-0014-9679
Ishfaq AhmadCancer Early Detection Advanced Research Center, Oregon Health and Science University, Oregon, OR, USA.
Isabel J DengosCancer Early Detection Advanced Research Center, Oregon Health and Science University, Oregon, OR, USA.
Andy RyanUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London (UCL), London, UK.
Sophia ApostolidouUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London (UCL), London, UK.
Aleksandra Gentry-MaharajDepartment of Women's Cancer, EGA Institute for Women's Health, University College London (UCL), London, UK.
Shannon HollowayDepartment of Population Health Sciences, Duke University, Durham, NC, USA.
Marc D RyserDepartment of Population Health Sciences, Duke University, Durham, NC, USA.ORCID http://orcid.org/0000-0002-4990-0849
Usha MenonUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London (UCL), London, UK.ORCID http://orcid.org/0000-0003-3708-1732
Ruth EtzioniDivision of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Funding

Modeling and analytics for cancer diagnostics: traversing the data-evidence divideR35CA274442 · NCI · FRED HUTCHINSON CANCER CENTER · PI RUTH D ETZIONI · 2022 to 2026
$4.9M
Cancer Research UK (CRUK) C1479/A2884DH | National Institute for Health Research (NIHR) NIHR HTA grant 16/46/01NCI NIH HHS R35 CA274442RCUK | Medical Research Council (MRC) G9901012 and G0801228U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R35CA274442
6 · The paper itself

Abstract

backgroundThe UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS; 2001-2020) showed no reduction in disease mortality in its primary intervention arm using multimodal screening (MMS) with longitudinal Cancer Antigen 125 (CA125) and transvaginal ultrasound. Whether this null result reflects the stop-screen design, screening performance, or ovarian cancer natural history remains unclear.

methodsUsing individual-level screening and diagnosis data from the MMS arm, we estimated ovarian cancer natural history, focusing on high-grade serous ovarian cancer (HGSC), the most common and lethal subtype. We then simulated trial outcomes under (1) continued screening beyond the trial screening interval and (2) high sensitivity for early-stage detection over an extended time period.

resultsThe estimated window for detecting early-stage HGSC under MMS was <6 months. Continued screening yielded at most a 15% relative mortality reduction. Achieving a ≥20% mortality reduction required extending the detectable early-stage window to 1 year and attaining ≥70% sensitivity during this period.

conclusionCurrent screening modalities offer a very limited opportunity to intercept HGSC at an early stage. Clinically effective ovarian cancer screening will require first- and second-line tests capable of detecting HGSC substantially earlier in its natural history.

Indexed as

Early Detection of CancerOvarian NeoplasmsAgedCA-125 AntigenFemaleHumansMass ScreeningMiddle AgedUnited KingdomCA-125 Antigen

Identifiers

PMID42288686
PMCPMC13464898

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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.