AGE AT DIAGNOSIS AS AN INDICATOR OF ELIGIBILITY FOR BRCA1 DNA TESTING IN FAMILIAL BREAST-CANCER

被引:21
作者
CORNELIS, RS
VASEN, HFA
MEIJERSHEIJBOER, H
FORD, D
VANVLIET, M
VANTILBORG, AAG
CLETON, FJ
KLIJN, JGM
MENKO, FH
KHAN, PM
CORNELISSE, CJ
DEVILEE, P
机构
[1] LEIDEN STATE UNIV,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
[2] LEIDEN UNIV,FDN DETECT HEREDITARY TUMORS,LEIDEN,NETHERLANDS
[3] ERASMUS UNIV ROTTERDAM,DEPT CLIN GENET,3000 DR ROTTERDAM,NETHERLANDS
[4] INST CANC RES,EPIDEMIOL SECT,SURREY,ENGLAND
[5] LEIDEN UNIV,DEPT CLIN ONCOL,LEIDEN,NETHERLANDS
[6] DEPT ENDOCRINE ONCOL,DANIEL DEN HOED KLIN,ROTTERDAM,NETHERLANDS
[7] FREE UNIV AMSTERDAM HOSP,DEPT CLIN GENET,AMSTERDAM,NETHERLANDS
[8] LEIDEN UNIV,DEPT PATHOL,LEIDEN,NETHERLANDS
关键词
D O I
10.1007/BF00223866
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:539 / 544
页数:6
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