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The avoiding late diagnosis of ovarian cancer (ALDO) project; a pilot national surveillance programme for women with pathogenic germline variants in BRCA1 and BRCA2.
Philpott, Sue; Raikou, Maria; Manchanda, Ranjit; Lockley, Michelle; Singh, Naveena; Scott, Malcolm; Evans, D Gareth; Adlard, Julian; Ahmed, Munaza; Edmondson, Richard; Woodward, Emma Roisin; Lamnisos, Athena; Balega, Janos; Brady, Angela F; Sharma, Aarti; Izatt, Louise; Kulkarni, Anjana; Tripathi, Vishakha; Solomons, Joyce S; Hayes, Kevin; Hanson, Helen; Snape, Katie; Side, Lucy; Skates, Steve; McGuire, Alistair; Rosenthal, Adam N.
  • Philpott S; North Central London Cancer Alliance, University College London Hospitals NHS Foundation Trust, London, UK.
  • Raikou M; Department of Economics, University of Piraeus, Athens, Greece.
  • Manchanda R; Health Economics, The London School of Economics and Political Science, London, UK.
  • Lockley M; Department of Gynaecological Oncology, Barts Health NHS Trust, London, UK.
  • Singh N; London School of Hygiene and Tropical Medicine, London, UK.
  • Scott M; Wolfsen Institue of Population Health Medicine, Barts CRUK Cancer Centre, Queen Mary University of London, London, UK.
  • Evans DG; Centre for Cancer genomics and Computational Biology, Barts Cancer Institute, Queen Mary University of London, London, London, UK.
  • Adlard J; Department of Cellular Pathology, Barts Health NHS Trust, London, London, UK.
  • Ahmed M; Familial Cancer Clinic, Department of Gynaecology, University College London Hospitals NHS Foundation Trust, London, London, UK.
  • Edmondson R; Division of Evolution and Genomic Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, Manchester, UK.
  • Woodward ER; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, Greater Manchester, UK.
  • Lamnisos A; Yorkshire Regional Genetics Service, Chapel Allerton Hospital, Leeds, West Yorkshire, UK.
  • Balega J; North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children, London, London, UK.
  • Brady AF; Division of Cancer Sciences, Faculty of Biology, Medicine and Health, St Mary's Hospital, University of Manchester, Manchester, UK, Manchester University NHS Foundation Trust, Manchester, Greater Manchester, UK.
  • Sharma A; Division of Evolution and Genomic Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, Manchester, UK.
  • Izatt L; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, Greater Manchester, UK.
  • Kulkarni A; The Eve Appeal, London, UK.
  • Tripathi V; Birmingham City Hospital, Birmingham, Birmingham, UK.
  • Solomons JS; North West Thames Regional Genetics Service, London North West University Healthcare NHS Trust, Harrow, London, UK.
  • Hayes K; University Hospital of Wales Healthcare NHS Trust, Heath Park, Cardiff, UK.
  • Hanson H; Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, London, UK.
  • Snape K; Medical and Molecular Genetics, King's College London Faculty of Life Sciences and Medicine, London, UK.
  • Side L; Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, London, UK.
  • Skates S; Department of Clinical Genetics, Guy's and St Thomas' Hospitals NHS Trust, London, London, UK.
  • McGuire A; Oxford Centre for Genomic Medicine (OXGeM), Oxford University Hospitals NHS Trust, Oxford, UK.
  • Rosenthal AN; St George's University Hospitals NHS Foundation Trust, London, London, UK.
J Med Genet ; 2022 Nov 01.
Article in English | MEDLINE | ID: covidwho-2301797
ABSTRACT

BACKGROUND:

Our study aimed to establish 'real-world' performance and cost-effectiveness of ovarian cancer (OC) surveillance in women with pathogenic germline BRCA1/2 variants who defer risk-reducing bilateral salpingo-oophorectomy (RRSO).

METHODS:

Our study recruited 875 female BRCA1/2-heterozygotes at 13 UK centres and via an online media campaign, with 767 undergoing at least one 4-monthly surveillance test with the Risk of Ovarian Cancer Algorithm (ROCA) test. Surveillance performance was calculated with modelling of occult cancers detected at RRSO. The incremental cost-effectiveness ratio (ICER) was calculated using Markov population cohort simulation.

RESULTS:

Our study identified 8 OCs during 1277 women screen years 2 occult OCs at RRSO (both stage 1a), and 6 screen-detected; 3 of 6 (50%) were ≤stage 3a and 5 of 6 (83%) were completely surgically cytoreduced. Modelled sensitivity, specificity, Positive Predictive Value (PPV) and Negative Predictive Value (NPV) for OC were 87.5% (95% CI, 47.3 to 99.7), 99.9% (99.9-100), 75% (34.9-96.8) and 99.9% (99.9-100), respectively. The predicted number of quality-adjusted life years (QALY) gained by surveillance was 0.179 with an ICER cost-saving of -£102,496/QALY.

CONCLUSION:

OC surveillance for women deferring RRSO in a 'real-world' setting is feasible and demonstrates similar performance to research trials; it down-stages OC, leading to a high complete cytoreduction rate and is cost-saving in the UK National Health Service (NHS) setting. While RRSO remains recommended management, ROCA-based surveillance may be considered for female BRCA-heterozygotes who are deferring such surgery.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Variants Language: English Year: 2022 Document Type: Article Affiliation country: Jmg-2022-108741

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Topics: Variants Language: English Year: 2022 Document Type: Article Affiliation country: Jmg-2022-108741