Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ

被引:72
作者
Claus, EB
Petruzella, S
Matloff, E
Carter, D
机构
[1] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, Yale Comprehens Canc Ctr, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
[3] Brigham & Womens Hosp, Dept Neurosurg, Boston, MA USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2005年 / 293卷 / 08期
关键词
D O I
10.1001/jama.293.8.964
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context The distribution of BRCA1 and BRCA2 mutations in women diagnosed with noninvasive breast carcinoma is unknown. Objective To estimate the BRCA1 and BRCA2 mutation prevalence in women with ductal carcinoma in situ (DCIS), unselected for age, family history, or ethnicity. Design, Setting, and Participants The data were 369 DCIS cases diagnosed among female residents aged 20 to 79 years from the state of Connecticut between September 15,1994, and March 14, 1998. These women were participants in a large population-based case-control study of breast carcinoma in situ. Telephone interviews were used to collect risk factor information and blood or buccal specimens were collected for BRCA1 and BRCA2 mutation testing. Main Outcome Measures Prevalence of disease-associated mutations of BRCA1 and BRCA2 in women diagnosed with DCIS. Results Three (0.8%) and 9 (2.4%) of 369 DCIS cases had disease-associated mutations in BRCA1 or BRCA2, respectively. One woman had a mutation in both genes (BRCA1 W321X and BRCA2 3398del5). Carriers were significantly more likely than noncarriers to report a first-degree (mother, sister, or daughter) family history of breast cancer (odds ratio [OR], 3.7; 95% confidence interval [CI], 1.1 -12.4), as well as a personal history of ovarian cancer. In addition, carriers were more likely than noncarriers to be diagnosed at an early age (<50 years) (OR, 3.4; 95% Cl, 1.0-11.7), as well as to report at least 1 first-degree relative diagnosed with breast cancer before 50 years (OR, 10.6; 95% Cl, 3.0-37.0). Conclusions Ductal carcinoma in situ is a part of the breast/ovarian cancer syndromes defined by BRCA1 and BRCA2, with mutation rates similar to those found for invasive breast cancer. These findings suggest that patients with breast cancer with an appropriate personal or family history of breast and/or ovarian cancer should be screened and followed according to high-risk protocols, regardless of whether they are diagnosed with in situ or invasive breast cancer.
引用
收藏
页码:964 / 969
页数:6
相关论文
共 54 条
[21]   Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2:: Analysis of 10,000 individuals [J].
Frank, TS ;
Deffenbaugh, AM ;
Reid, JE ;
Hulick, M ;
Ward, BE ;
Lingenfelter, B ;
Gumpper, KL ;
Scholl, T ;
Tavtigian, SV ;
Pruss, DR ;
Critchfield, GC .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) :1480-1490
[22]   Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes [J].
Friedman, E ;
Bruchim, RB ;
Kruglikova, A ;
Risel, S ;
Levy-Lahad, E ;
Halle, D ;
Bar-On, E ;
Gershoni-Baruch, R ;
Dagan, E ;
Kepten, I ;
Peretz, T ;
Lerer, I ;
Wienberg, N ;
Shushan, A ;
Abeliovich, D .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) :1224-1227
[23]  
Ganguly A, 2001, AM J MED GENET, V101, P146, DOI 10.1002/1096-8628(20010615)101:2<146::AID-AJMG1342>3.0.CO
[24]  
2-E
[25]   Co-segregation of BRCA1 185delAG mutation and BRCA2 6174delT in one single family [J].
Gershoni-Baruch, R ;
Dagan, E ;
Kepten, I ;
Freid, G .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (13) :2283-2284
[26]   High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancer [J].
Hoogerbrugge, N ;
Bult, P ;
de Widt-Levert, LM ;
Beex, LV ;
Kiemeney, LA ;
Ligtenberg, MJL ;
Massuger, LF ;
Boetes, C ;
Manders, P ;
Brunner, HG .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (01) :41-45
[27]   Intraductal component and BRCA1-associated breast cancer [J].
Jacquemier, J ;
Eisinger, F ;
Guinebretier, JM ;
StoppaLyonnet, D ;
Sobol, H .
LANCET, 1996, 348 (9034) :1098-1098
[28]  
Johannesdottir G, 1996, CANCER RES, V56, P3663
[29]   Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2 [J].
King, MC ;
Marks, JH ;
Mandell, JB .
SCIENCE, 2003, 302 (5645) :643-646
[30]   Differential contributions of BRCA1 and BRCA2 to early-onset breast cancer [J].
Krainer, M ;
SilvaArrieta, S ;
FitzGerald, MG ;
Shimada, A ;
Ishioka, C ;
Kanamaru, R ;
MacDonald, DJ ;
Unsal, H ;
Finkelstein, DM ;
Bowcock, A ;
Isselbacher, KJ ;
Haber, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (20) :1416-1421