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Performance Characteristics of the Ultrasound Strategy during Incidence Screening in the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS).
Kalsi, Jatinderpal; Gentry-Maharaj, Aleksandra; Ryan, Andy; Singh, Naveena; Burnell, Matthew; Massingham, Susan; Apostolidou, Sophia; Sharma, Aarti; Williamson, Karin; Seif, Mourad; Mould, Tim; Woolas, Robert; Dobbs, Stephen; Leeson, Simon; Fallowfield, Lesley; Skates, Steven J; Parmar, Mahesh; Campbell, Stuart; Jacobs, Ian; McGuire, Alistair; Menon, Usha.
Affiliation
  • Kalsi J; Department of Women's Cancer, Institute for Women's Health, University College London, London WC1E 6HU, UK.
  • Gentry-Maharaj A; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
  • Ryan A; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
  • Singh N; Department of Pathology, Barts and the London, London E1 2ES, UK.
  • Burnell M; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
  • Massingham S; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
  • Apostolidou S; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
  • Sharma A; Department of Obstetrics and Gynaecology, University Hospital of Wales, Cardiff CF14 4XW, UK.
  • Williamson K; Department of Gynaecological Oncology, Nottingham City Hospital, Nottingham NG5 1PB, UK.
  • Seif M; Division of Gynaecology and of Cancer Services, St. Mary's Hospital and University of Manchester, Manchester M13 9WL, UK.
  • Mould T; Department of Gynaecological Oncology, University College Hospital, London NW1 2BU, UK.
  • Woolas R; Department of Gynaecological Oncology, Queen Alexandra Hospital, Portsmouth PO6 3LY, UK.
  • Dobbs S; Department of Gynaecological Oncology, Belfast City Hospital, Belfast BT9 7AB, UK.
  • Leeson S; Department of Obstetrics and Gynaecology, Ysbyty Gwynedd, Bangor, Gwynedd LL57 2PW, UK.
  • Fallowfield L; Cancer Research UK Sussex Psychosocial Oncology Group at Brighton & Sussex Medical School, University of Sussex, Falmer BN1 9PX, UK.
  • Skates SJ; Massachusetts General Hospital, Harvard Medical School, Boston, MA 02115, USA.
  • Parmar M; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London WC1V 6LJ, UK.
  • Campbell S; Create Fertility Clinic, London EC2V 6ET, UK.
  • Jacobs I; Department of Women's Cancer, Institute for Women's Health, University College London, London WC1E 6HU, UK.
  • McGuire A; Department of Women's Health, University of New South Wales, Australia, Sydney 2052, Australia.
  • Menon U; London School of Economics and Political Science, London WC2A 2AE, UK.
Cancers (Basel) ; 13(4)2021 Feb 18.
Article in En | MEDLINE | ID: mdl-33670571
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Language: En Journal: Cancers (Basel) Year: 2021 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Diagnostic_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Language: En Journal: Cancers (Basel) Year: 2021 Document type: Article Affiliation country: United kingdom