1. Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer
- Author
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R. S. Cornells, H. F. A. Vasen, H. Meijers-Heijboer, D. Ford, M. van Vliet, A. A. G. van Tilborg, F. J. Cleton, J. G. M. Klijn, F. H. Menko, P. Meera Khan, C. J. Cornelisse, P. Devilee, and Other departments
- Subjects
Adult ,Male ,Oncology ,medicine.medical_specialty ,endocrine system diseases ,Genetic Linkage ,DNA Mutational Analysis ,Mammary gland ,Breast Neoplasms ,Biology ,Breast Neoplasms, Male ,Breast cancer ,Internal medicine ,Genetics ,medicine ,Humans ,Age of Onset ,Family history ,skin and connective tissue diseases ,Genetics (clinical) ,Netherlands ,Ovarian Neoplasms ,BRCA1 Protein ,Cancer ,DNA, Neoplasm ,Middle Aged ,medicine.disease ,Neoplasm Proteins ,Pedigree ,Chromosome 17 (human) ,medicine.anatomical_structure ,Female ,Lod Score ,Age of onset ,Ovarian cancer ,Chromosomes, Human, Pair 17 ,Transcription Factors ,Founder effect - Abstract
We searched for criteria that could indicate breast cancer families with a high prior probability of being caused by the breast/ovarian cancer susceptibility locus BRCA1 on chromosome 17. To this end, we performed a linkage study with 59 consecutively collected Dutch breast cancer families, including 16 with at least one case of ovarian cancer. We used an intake cut-off of at least three first-degree relatives with breast and/or ovarian cancer at any age. Significant evidence for linkage was found only among the 13 breast cancer families with a mean age at diagnosis of less than 45 years. An unexpectedly low proportion of the breast-ovarian cancer families were estimated to be linked to BRCA1, which could be due to a founder effect in the Dutch population. Given the expected logistical problems in clinical management now that BRCA1 has been identified, we propose an interim period in which only families with a strong positive family history for early onset breast and/or ovarian cancer will be offered BRCA1 mutation testing.
- Published
- 1995
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