Predictive factors for BRCA1/BRCA2 mutations in women with ductal carcinoma in situ

被引:21
作者
Bayraktar, Soley [2 ]
Elsayegh, Nisreen [1 ]
Barrera, Angelica M. Gutierrez [1 ]
Lin, Heather [3 ]
Kuerer, Henry [4 ]
Tasbas, Tunc
Muse, Kimberly I. [1 ]
Ready, Kaylene [1 ]
Litton, Jennifer [1 ]
Meric-Bernstam, Funda [4 ]
Hortobagyi, Gabriel N. [1 ]
Albarracin, Constance T. [5 ]
Arun, Banu [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Div Canc Med, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
关键词
ductal carcinoma in situ; BRCA; 1; 2; mutations; BRCAPRO; family history; predictive factors; BRCA2; MUTATIONS; BREAST-CANCER; OVARIAN-CANCER; HIGH PREVALENCE; CARRIERS; LESIONS; RISK;
D O I
10.1002/cncr.26428
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: It is unclear whether women with ductal carcinoma in situ (DCIS), like their counterparts with invasive breast cancer, warrant genetic risk assessment and testing on the basis of high-risk variables. The authors of this report identified predictive factors for mutations in the breast cancer-susceptibility genes BRCA1 and BRCA2 in women who were diagnosed with DCIS. METHODS: One hundred eighteen women with DCIS who were referred for genetic counseling and underwent genetic testing for BRCA1/BRCA2 mutations between 2003 and 2010 were included in the study. Logistic regression models were fit to determine the associations between potential predictive factors and BRCA status. RESULTS: Of 118 high-risk women with DCIS, 27% (n 32) tested positive for BRCA1/BRCA2 mutations. Of those, 10% (n 12) and 17% (n 20) had BRCA1 and BRCA2 mutations, respectively. Age, race, and tumor characteristics did not differ between BRCA noncarriers and carriers. In a multivariate logistic model, 2 relatives with ovarian cancer (OC) (odds ratio [OR], 8.81; 95% confidence interval [CI], 1.38-56.29; P.034), and a score >= 10% according to the BRCAPRO mathematical model for calculating the probability that a particular family member carries a germline BRCA mutation (OR, 6.37; 95% CI, 2.23-18.22; P.0005) remained as independent significant predictors for a BRCA mutation. Fifty-seven percent of mutation carriers but only 25% of noncarriers underwent prophylactic mastectomy(P.0037). This difference remained significant for patients aged <= 40 years (P.025). CONCLUSIONS: Women who had DCIS and a family history of OC or who had BRCAPRO scores >= 10% had a high rate of BRCA positivity regardless of age at diagnosis. These findings suggest that high-risk patients with DCIS are appropriate candidates for genetic testing for BRCA mutations in the presence of predictive factors even if they do not have invasive breast cancer. Cancer 2012; 118: 1515-22. VC 2011 American Cancer Society.
引用
收藏
页码:1515 / 1522
页数:8
相关论文
共 26 条
  • [1] Pathologic characteristics of breast parenchyma in patients with hereditary breast carcinoma, including BRCA1 and BRCA2 mutation carriers
    Adem, C
    Reynolds, C
    Soderberg, CL
    Slezak, JM
    McDonnell, SK
    Sebo, TJ
    Schaid, DJ
    Myers, JL
    Sellers, TA
    Hartmann, LC
    Jenkins, RB
    [J]. CANCER, 2003, 97 (01) : 1 - 11
  • [2] [Anonymous], 1980, STAT METHODS
  • [3] High Prevalence of Preinvasive Lesions Adjacent to BRCA1/2-Associated Breast Cancers
    Arun, Banu
    Vogel, Kristen J.
    Lopez, Adriana
    Hernandez, Mike
    Atchley, Deann
    Broglio, Kristine R.
    Amos, Christopher I.
    Meric-Bernstam, Funda
    Kuerer, Henry
    Hortobagyi, Gabriel N.
    Albarracin, Constance T.
    [J]. CANCER PREVENTION RESEARCH, 2009, 2 (02) : 122 - 127
  • [4] Characterization of BRCA1 and BRCA2 mutations in a large United States sample
    Chen, SN
    Iversen, ES
    Friebel, T
    Finkelstein, D
    Weber, BL
    Eisen, A
    Peterson, LE
    Schildkraut, JM
    Isaacs, C
    Peshkin, BN
    Corio, C
    Leondaridis, L
    Tomlinson, G
    Dutsm, D
    Kerber, R
    Amos, CI
    Strong, LC
    Berry, DA
    Euthus, DM
    Parmigiani, G
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (06) : 863 - 871
  • [5] Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ
    Claus, EB
    Petruzella, S
    Matloff, E
    Carter, D
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 293 (08): : 964 - 969
  • [6] The natural history of ductal carcinoma in situ of the breast:: a review
    Erbas, B
    Provenzan, E
    Armes, J
    Gertig, D
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2006, 97 (02) : 135 - 144
  • [7] Pretest prediction of BRCA1 or BRCA2 mutation by risk counselors and the computer model BRCAPRO
    Euhus, DM
    Smith, KC
    Robinson, L
    Stucky, A
    Olopade, OI
    Cummings, S
    Garber, JE
    Chittenden, A
    Mills, GB
    Rieger, P
    Esserman, L
    Crawford, B
    Hughes, KS
    Roche, CA
    Ganz, PA
    Seldon, J
    Fabian, CJ
    Klemp, J
    Tomlinson, G
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2002, 94 (11) : 844 - 851
  • [8] Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
    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
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) : 676 - 689
  • [9] Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2:: Analysis of 10,000 individuals
    Frank, TS
    Deffenbaugh, AM
    Reid, JE
    Hulick, M
    Ward, BE
    Lingenfelter, B
    Gumpper, KL
    Scholl, T
    Tavtigian, SV
    Pruss, DR
    Critchfield, GC
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) : 1480 - 1490
  • [10] Prevalence of BRCA1 and BRCA2 Mutations in Women with Breast Carcinoma In Situ and Referred for Genetic Testing
    Hall, Michael J.
    Reid, Julia E.
    Wenstrup, Richard J.
    [J]. CANCER PREVENTION RESEARCH, 2010, 3 (12) : 1579 - 1585