Evidence map›Paper›PMID 33670571›Full record

ArticleCancers2021

Performance Characteristics of the Ultrasound Strategy during Incidence Screening in the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS).

Jatinderpal Kalsi, Aleksandra Gentry-Maharaj, Andy Ryan, Naveena Singh, Matthew Burnell, Susan Massingham, Sophia Apostolidou, Aarti Sharma, Karin Williamson, Mourad Seif and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Early Detection of Ovarian Cancer.Cold Spring Harbor perspectives in medicine · 2023
    Review
  2. 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

21 authors at 15 institutions in 3 countries.

Jatinderpal KalsiDepartment of Women's Cancer, Institute for Women's Health, University College London, London WC1E 6HU, UK.
Aleksandra Gentry-MaharajMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.ORCID 0000-0001-7270-9762
Andy RyanMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
Naveena SinghDepartment of Pathology, Barts and the London, London E1 2ES, UK.
Matthew BurnellMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
Susan MassinghamMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
Sophia ApostolidouMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
Aarti SharmaDepartment of Obstetrics and Gynaecology, University Hospital of Wales, Cardiff CF14 4XW, UK.
Karin WilliamsonDepartment of Gynaecological Oncology, Nottingham City Hospital, Nottingham NG5 1PB, UK.
Mourad SeifDivision of Gynaecology and of Cancer Services, St. Mary's Hospital and University of Manchester, Manchester M13 9WL, UK.
Tim MouldDepartment of Gynaecological Oncology, University College Hospital, London NW1 2BU, UK.
Robert WoolasDepartment of Gynaecological Oncology, Queen Alexandra Hospital, Portsmouth PO6 3LY, UK.
Stephen DobbsDepartment of Gynaecological Oncology, Belfast City Hospital, Belfast BT9 7AB, UK.
Simon LeesonDepartment of Obstetrics and Gynaecology, Ysbyty Gwynedd, Bangor, Gwynedd LL57 2PW, UK.ORCID 0000-0002-5232-2330
Lesley FallowfieldCancer Research UK Sussex Psychosocial Oncology Group at Brighton & Sussex Medical School, University of Sussex, Falmer BN1 9PX, UK.
Steven J SkatesMassachusetts General Hospital, Harvard Medical School, Boston, MA 02115, USA.
Mahesh ParmarMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
Stuart CampbellCreate Fertility Clinic, London EC2V 6ET, UK.
Ian JacobsDepartment of Women's Cancer, Institute for Women's Health, University College London, London WC1E 6HU, UK.
Alistair McGuireLondon School of Economics and Political Science, London WC2A 2AE, UK.
Usha MenonMRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.ORCID 0000-0003-3708-1732
MRC Clinical Trials Unit at UCL · GBBarts Health NHS Trust · GBBrighton and Sussex Medical School · GBCREATe Centre · GBHarvard University · USLondon School of Economics and Political Science · GBLondon Women's Clinic · GBNottingham City Hospital · GBQueen Alexandra Hospital · GBUniversity College Hospital · GBUniversity Hospital of Wales · GBUniversity of Manchester · GBUniversity of Ulster · GBUNSW Sydney · AUYsbyty Gwynedd Hospital NHS Trust · GB

Funding

Cancer Research UK C1479/A2884Department of Health 16/46/01Department of Health N/AMedical Research Council G0000735Medical Research Council G0801228Medical Research Council G9901012Medical Research Council MC_UU_00004/01Medical Research Council MC_UU_12023/20Medical Research Council MC_UU_12023/28MRC CTU at UCL core funding ) MR_UU_12023National Institute for Health Research 16/46/01NIHR University College London Hospitals (UCLH) Biomedical Research Centre funding N/AThe Eve Appeal N/A
6 · The paper itself

Abstract

Randomised controlled trials of ovarian cancer (OC) screening have not yet demonstrated an impact on disease mortality. Meanwhile, the screening data from clinical trials represents a rich resource to understand the performance of modalities used. We report here on incidence screening in the ultrasound arm of UKCTOCS. 44,799 of the 50,639 women who were randomised to annual screening with transvaginal ultrasound attended annual incidence screening between 28 April 2002 and 31 December 2011. Transvaginal ultrasound was used both as the first and the second line test. Participants were followed up through electronic health record linkage and postal questionnaires. Out of 280,534 annual incidence screens, 960 women underwent screen-positive surgery. 113 had ovarian/tubal cancer (80 invasive epithelial). Of the screen-detected invasive epithelial cancers, 37.5% (95% CI: 26.9-49.0) were Stage I/II. An additional 52 (50 invasive epithelial) were diagnosed within one year of their last screen. Of the 50 interval epithelial cancers, 6.0% (95% CI: 1.3-16.5) were Stage I/II. For detection of all ovarian/tubal cancers diagnosed within one year of screen, the sensitivity, specificity, and positive predictive values were 68.5% (95% CI: 60.8-75.5), 99.7% (95% CI: 99.7-99.7), and 11.8% (95% CI: 9.8-14) respectively. When the analysis was restricted to invasive epithelial cancers, sensitivity, specificity and positive predictive values were 61.5% (95% CI: 52.6-69.9); 99.7% (95% CI: 99.7-99.7) and 8.3% (95% CI: 6.7-10.3), with 12 surgeries per screen positive. The low sensitivity coupled with the advanced stage of interval cancers suggests that ultrasound scanning as the first line test might not be suitable for population screening for ovarian cancer. Trial registration: ISRCTN22488978. Registered on 6 April 2000.

Indexed as

early detectionovarian cancerrandomised controlled trialscreeningtrialTVSUKCTOCSultrasound

Identifiers

PMID33670571
PMCPMC7922843
OpenAlexW3131503135

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.