Familial risks, early-onset breast cancer, and BRCA1 and BRCA2 germline mutations

被引:135
作者
Dite, GS
Jenkins, MA
Southey, MC
Hocking, JS
Giles, GG
McCredie, MRE
Venter, DJ
Hopper, JL
机构
[1] Univ Melbourne, Ctr Genet Epidemiol, Melbourne, Vic 3053, Australia
[2] Univ Melbourne, Dept Pathol, Genet Epidemiol Unit, Melbourne, Vic 3053, Australia
[3] Macfarlane Burnet Ctr Med Res, Melbourne, Vic, Australia
[4] Canc Council Victoria, Canc Epidemiol Ctr, Melbourne, Vic, Australia
[5] Univ Otago, Dept Prevent & Social Med, Dunedin, New Zealand
关键词
D O I
10.1093/jnci/95.6.448
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Having a family history of breast cancer, particularly if it involves early-onset disease, is a risk factor for breast cancer, but little is known about specific causes of this association. Consequently, we studied mothers, sisters, and aunts of an age-stratified sample of 1567 unselected case patients diagnosed with breast cancer before age 60 years, recruited to a population-based, case-control-family study, in which case patients, control subjects, and their relatives were administered the same questionnaire. Methods: Extensive BRCA1 and BRCA2 mutation testing was carried out for 788 case patients diagnosed before age 40 years, including manual sequencing of DNA from 72 patients with two or more affected relatives. Standardized morbidity ratios, age-specific cumulative risks, and hazard ratios were calculated for groupings of relatives. Results: Cumulative risks of breast cancer to age 50 years in the sisters, mothers, and aunts of the case patients, respectively, were 6, 3, and 2 times the population risk if the case patient was younger than age 40 years at diagnosis but were considerably lower if the case patient was older at diagnosis. When relatives of the case patients with a BRCA1 or BRCA2 mutation were excluded, these risks fell by, at most, 20%. Sisters and aunts, but not mothers, who had an additional first-degree relative with breast cancer were at increased risk, and the risk was greater when that relative was younger at diagnosis. Hazard ratios were 10.7 (95% confidence interval [CI] = 4.2 to 26.8) for sisters and 4.2 (95% CI = 2.2 to 8.1) for aunts, if the relative was aged 40 years at diagnosis. Fewer than one-third of the excess of breast cancers in relatives of case patients diagnosed before age 40 years that are attributed to familial factors are BRCA1- or BRCA2-related. Conclusion: Mutations in genes other than BRCA1 and BRCA2 may be associated with a high risk of breast cancer, especially in young women.
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页码:448 / 457
页数:10
相关论文
共 30 条
[1]   A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes [J].
Antoniou, AC ;
Pharoah, PDP ;
McMullan, G ;
Day, NE ;
Stratton, MR ;
Peto, J ;
Ponder, BJ ;
Easton, DF .
BRITISH JOURNAL OF CANCER, 2002, 86 (01) :76-83
[2]  
Armes JE, 1998, CANCER-AM CANCER SOC, V83, P2335, DOI 10.1002/(SICI)1097-0142(19981201)83:11<2335::AID-CNCR13>3.0.CO
[3]  
2-N
[4]   Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58 209 women with breast cancer and 101 986 women without the disease [J].
Beral, V ;
Bull, D ;
Doll, R ;
Peto, R ;
Reeves, G .
LANCET, 2001, 358 (9291) :1389-1399
[5]   Effect of BRCA1 and BRCA2 on the association between breast cancer risk and family history [J].
Claus, EB ;
Schildkraut, J ;
Iversen, ES ;
Berry, D ;
Parmigiani, G .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (23) :1824-1829
[6]   AGE AT ONSET AS AN INDICATOR OF FAMILIAL RISK OF BREAST-CANCER [J].
CLAUS, EB ;
RISCH, NJ ;
THOMPSON, D .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1990, 131 (06) :961-972
[7]  
Cleveland W. S., 1993, VISUALISING DATA
[8]   After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer [J].
Cui, JS ;
Antoniou, AC ;
Dite, GS ;
Southey, MC ;
Venter, DJ ;
Easton, DF ;
Giles, GG ;
McCredie, MRE ;
Hopper, JL .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (02) :420-431
[9]  
EASTON DF, 1993, AM J HUM GENET, V52, P678
[10]   Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families [J].
Ford, D ;
Easton, DF ;
Stratton, M ;
Narod, S ;
Goldgar, D ;
Devilee, P ;
Bishop, DT ;
Weber, B ;
Lenoir, G ;
Chang-Claude, J ;
Sobol, H ;
Teare, MD ;
Struewing, J ;
Arason, A ;
Scherneck, S ;
Peto, J ;
Rebbeck, TR ;
Tonin, P ;
Neuhausen, S ;
Barkardottir, R ;
Eyfjord, J ;
Lynch, H ;
Ponder, BAJ ;
Gayther, SA ;
Birch, JM ;
Lindblom, A ;
Stoppa-Lyonnet, D ;
Bignon, Y ;
Borg, A ;
Hamann, U ;
Haites, N ;
Scott, RJ ;
Maugard, CM ;
Vasen, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) :676-689