Prevalence of <i>BRCA1/2</i> germline mutations in 21 401 families with breast and ovarian cancer

Karin Kast(German Cancer Research Center), Kerstin Rhiem(University of Cologne), Barbara Wappenschmidt(University of Cologne), Eric Hahnen(University of Cologne), Jan Hauke(University of Cologne), Britta Bluemcke(University of Cologne), V Zarghooni(University of Cologne), N Herold(University of Cologne), Nina Ditsch(LMU Klinikum), Marion Kiechle(Technical University of Munich), Michael Braun(German Red Cross), Christine Fischer(Heidelberg University), Nicola Dikow(Heidelberg University), Sarah Schott(German Cancer Research Center), Nils Rahner(Heinrich Heine University Düsseldorf), Dieter Niederacher(Heinrich Heine University Düsseldorf), Tanja Fehm(Heinrich Heine University Düsseldorf), Andrea Gehrig(University of Würzburg), Clemens Mueller-Reible(University of Würzburg), Norbert Arnold(Christian-Albrechts-Universität zu Kiel), Nicolaì Maass(Christian-Albrechts-Universität zu Kiel), Guntram Borck(Universität Ulm), Nikolaus de Gregorio(Universität Ulm), Caroline Scholz(Medizinische Hochschule Hannover), Bernd Auber(Medizinische Hochschule Hannover), Raymonda Varon-Manteeva(University Medical Center), Dorothee Speiser(Charité - Universitätsmedizin Berlin), Judit Horváth(University of Münster), Nadine Lichey(University of Münster), Pauline Wimberger(German Cancer Research Center), Sylvia Stark(Leipzig University), Ulrike Faust(Genomics (United Kingdom)), Bernhard H. F. Weber(University of Regensburg), Günter Emons(University of Göttingen), Silke Zachariae(Leipzig University), Alfons Meindl(Technical University of Munich), Rita K. Schmutzler(University of Cologne), Christoph Engel(Leipzig University)
Journal of Medical Genetics
February 29, 2016
Cited by 223

Abstract

PURPOSE: To characterise the prevalence of pathogenic germline mutations in BRCA1 and BRCA2 in families with breast cancer (BC) and ovarian cancer (OC) history. PATIENTS AND METHODS: Data from 21 401 families were gathered between 1996 and 2014 in a clinical setting in the German Consortium for Hereditary Breast and Ovarian Cancer, comprising full pedigrees with cancer status of all individual members at the time of first counselling, and BRCA1/2 mutation status of the index patient. RESULTS: The overall BRCA1/2 mutation prevalence was 24.0% (95% CI 23.4% to 24.6%). Highest mutation frequencies were observed in families with at least two OCs (41.9%, 95% CI 36.1% to 48.0%) and families with at least one breast and one OC (41.6%, 95% CI 40.3% to 43.0%), followed by male BC with at least one female BC or OC (35.8%; 95% CI 32.2% to 39.6%). In families with a single case of early BC (<36 years), mutations were found in 13.7% (95% CI 11.9% to 15.7%). Postmenopausal unilateral or bilateral BC did not increase the probability of mutation detection. Occurrence of premenopausal BC and OC in the same woman led to higher mutation frequencies compared with the occurrence of these two cancers in different individuals (49.0%; 95% CI 41.0% to 57.0% vs 31.5%; 95% CI 28.0% to 35.2%). CONCLUSIONS: Our data provide guidance for healthcare professionals and decision-makers to identify individuals who should undergo genetic testing for hereditary breast and ovarian cancer. Moreover, it supports informed decision-making of counselees on the uptake of genetic testing.


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