Evidence map›Paper›PMID 38834293›Full record

ArticleJournal of medical genetics2024

Validation of the BOADICEA model in a prospective cohort of

Xin Yang, Thea M Mooij, Goska Leslie, Lorenzo Ficorella, Nadine Andrieu, Karin Kast, Christian F Singer, Anna Jakubowska, Carla H van Gils, Yen Y Tan and 32 more

Abstract readValidation Study
In one paragraph

Article in Journal of medical genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Trial
  2. Polygenic scores as modifiers in Mendelian diseases.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2026
    Article
  3. Polygenic risk scores in clinical applications - opportunities and challenges.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. 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

42 authors.

Xin YangCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK xy249@medschl.cam.ac.uk.ORCID 0000-0003-0037-3790
Thea M MooijDepartment of Epidemiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Goska LeslieCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.
Lorenzo FicorellaCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.ORCID 0000-0002-0577-1571
Nadine AndrieuINSERM U900, Paris, France.
Karin KastCenter for Hereditary Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), Medical Faculty, University Hospital Cologne, Cologne, Germany.
Christian F SingerDepartment of OB/GYN and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Anna JakubowskaDepartment of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
Carla H van GilsJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.
Yen Y TanDepartment of OB/GYN and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Christoph EngelInstitute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.
Muriel A AdankDepartment of Clinical Genetics, The Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Christi J van AsperenDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Margreet G E M AusemsDevision Laboratories, Pharmacy and Biomedical Genetics, Department of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
Pascaline BerthetOncogénétique Département de Biopathologie, Centre François Baclesse, Caen, France.
EMBRACE collaborators
Margriet J ColleeDepartment of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
Jackie A CookSheffield Clinical Genetics Service, Scheffield Children's Hospital, Sheffield, UK.
Jacqueline EasonNottingham Clinical Genetics Service, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Karin Y van Spaendonck-ZwartsDepartment of Human Genetics, Amsterdam University Medical Centres, Amsterdam, The Netherlands.
D Gareth EvansThe Prevent Breast Cancer Research Unit, The Nightingale Centre, Manchester University NHS Foundation Trust, Manchester, UK.
Encarna B Gómez GarcíaDepartment of Clinical Genetics, Maastricht University, Maastricht, The Netherlands.
Helen HansonSouth West Thames Regional Genetics Service, St George's University Hospitals NHS Foundation Trust, London, UK.ORCID 0000-0002-3303-8713
Louise IzattDepartment of Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-1258-4843
Zoe KempDepartment of Cancer Genetics, Royal Marsden Hospital, NHS Trust, London, UK.ORCID 0000-0003-2692-0369
Fiona LallooClinical Genetics Service, Manchester Centre for Genomic Medicine, Manchester University Hospitals Foundation Trust, Manchester, UK.
Christine LassetUniversité Claude Bernard Lyon 1, Villeurbanne, France.
Fabienne LesueurINSERM U900, Paris, France.
Hannah MusgraveYorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Sophie NambotCentre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, CHU de Dijon, Hôpital d'Enfants, Dijon, France.
Catherine NoguèsDépartement d'Anticipation et de Suivi des Cancers, Oncogénétique Clinique, Institut Paoli Calmettes, Marseille, France.
Jan C OosterwijkDepartment of Genetics, University of Groningen, University Medical Center, Groningen, The Netherlands.
Dominique Stoppa-LyonnetInstitut Curie, Service de Génétique, Paris, France.
Marc TischkowitzDepartment of Medical Genetics, National Institute for Health Research Cambridge Biomedical Research Centre, University of Cambridge, Cambridge, UK.
Vishakha TripathiClinical Genetics Service, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Marijke R WeversDepartment of Clinical Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Emily ZhaoCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.
Flora E van LeeuwenDepartment of Epidemiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Marjanka K SchmidtDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Douglas F EastonCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.
Matti A RookusDepartment of Epidemiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Antonis C AntoniouCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Strangeways Research Laboratory, Cambridge, UK.ORCID 0000-0001-9223-3116

Funding

Cancer Research UK 20861
6 · The paper itself

Abstract

backgroundNo validation has been conducted for the BOADICEA multifactorial breast cancer risk prediction model specifically in

methodsWe evaluated the model calibration and discriminatory ability in the prospective TRANsIBCCS cohort study comprising 1614

resultsThe full multifactorial model considering family history together with all other risk factors was well calibrated overall (E/O=1.07, 95% CI: 0.92 to 1.24) and in quintiles of predicted risk. Discrimination was maximised when all risk factors were considered (Harrell's C-index=0.70, 95% CI: 0.67 to 0.74; area under the curve=0.79, 95% CI: 0.76 to 0.82). The model performance was similar when evaluated separately in

conclusionBOADICEA may be used to aid personalised cancer risk management and decision-making for

Indexed as

BRCA1 ProteinBRCA2 ProteinBreast NeoplasmsGenetic Predisposition to DiseaseHeterozygoteAdultFemaleHumansMiddle AgedPolymorphism, Single NucleotideProspective StudiesRisk AssessmentRisk FactorsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanEarly DiagnosisGenetic CounselingPublic HealthWomen's Health

Identifiers

PMID38834293
PMCPMC11287562

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.