Performance of Prediction Models for BRCA Mutation Carriage in Three Racial/Ethnic Groups: Findings from the Northern California Breast Cancer Family Registry

被引:59
作者
Kurian, Allison W. [1 ,2 ]
Gong, Gail D. [1 ]
John, Esther M. [1 ,4 ]
Miron, Alexander [3 ]
Felberg, Anna [1 ]
Phipps, Amanda I. [4 ]
West, Dee W. [1 ,4 ]
Whittemore, Alice S. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] No Calif Canc Ctr, Fremont, CA USA
关键词
SENSITIVE GEL-ELECTROPHORESIS; GENETIC SUSCEPTIBILITY; RISK-ASSESSMENT; SCORING SYSTEM; BOADICEA MODEL; PREVALENCE; VALIDATION; AMERICAN; INDIVIDUALS; PROBABILITY;
D O I
10.1158/1055-9965.EPI-08-1090
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Patients with early-onset breast and/or ovarian cancer frequently wish to know if they inherited a mutation in one of the cancer susceptibility genes, BRCA1 or BRCA2. Accurate carrier prediction models are needed to target costly testing. Two widely used models, BRCAPRO and BOADICEA, were developed using data from non-Hispanic Whites (NHW), but their accuracies have not been evaluated in other racial/ethnic populations. Methods: We evaluated the BRCAPRO and BOADICEA models in a population-based series of African American, Hispanic, and NHW breast cancer patients tested for BRCA1 and BRCA2 mutations. We assessed model calibration by evaluating observed versus predicted mutations and attribute diagrams, and model discrimination using areas under the receiver operating characteristic curves. Results: Both models were well-calibrated within each racial/ethnic group, with some exceptions. BOADICEA overpredicted mutations in African Americans and older NHWs, and BRCAPRO underpredicted in Hispanics. In all racial/ethnic groups, the models overpredicted in cases whose personal and family histories indicated >80% probability of carriage. The two models showed similar discrimination in each racial/ethnic group, discriminating least well in Hispanics. For example, BRCAPRO's areas under the receiver operating characteristic curves were 83% (95% confidence interval, 63-93%) for NHWs, compared with 74% (59-85%) for African Americans and 58% (45-70%) for Hispanics. Conclusions: The poor performance of the model for Hispanics may be due to model misspecification in this racial/ethnic group. However, it may also reflect racial/ ethnic differences in the distributions of personal and family histories among breast cancer cases in the Northern California population. (Cancer Epidemiol Biomarkers Prev 2009;18(4):1084-91)
引用
收藏
页码:1084 / 1091
页数:8
相关论文
共 44 条
[1]   Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations [J].
Andrulis, IL ;
Anton-Culver, H ;
Beck, J ;
Bove, B ;
Boyd, J ;
Buys, S ;
Godwin, AK ;
Hopper, JL ;
Li, F ;
Neuhausen, SL ;
Ozcelik, H ;
Peel, D ;
Santella, RM ;
Southey, MC ;
van Orsouw, NJ ;
Venter, DJ ;
Vijg, J ;
Whittemore, AS .
HUMAN MUTATION, 2002, 20 (01) :65-73
[2]   Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation:: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics [J].
Antoniou, A. C. ;
Hardy, R. ;
Walker, L. ;
Evans, D. G. ;
Shenton, A. ;
Eeles, R. ;
Shanley, S. ;
Pichert, G. ;
Izatt, L. ;
Rose, S. ;
Douglas, F. ;
Eccles, D. ;
Morrison, P. J. ;
Scott, J. ;
Zimmern, R. L. ;
Easton, D. F. ;
Pharoah, P. D. P. .
JOURNAL OF MEDICAL GENETICS, 2008, 45 (07) :425-431
[3]   The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions [J].
Antoniou, A. C. ;
Cunningham, A. P. ;
Peto, J. ;
Evans, D. G. ;
Lalloo, F. ;
Narod, S. A. ;
Risch, H. A. ;
Eyfjord, J. E. ;
Hopper, J. L. ;
Southey, M. C. ;
Olsson, H. ;
Johannsson, O. ;
Borg, A. ;
Passini, B. ;
Radice, P. ;
Manoukian, S. ;
Eccles, D. M. ;
Tang, N. ;
Olah, E. ;
Anton-Culver, H. ;
Warner, E. ;
Lubinski, J. ;
Gronwald, J. ;
Gorski, B. ;
Tryggvadottir, L. ;
Syrjakoski, K. ;
Kallioniemi, O-P ;
Eerola, H. ;
Nevanlinna, H. ;
Pharoah, P. D. P. ;
Easton, D. F. .
BRITISH JOURNAL OF CANCER, 2008, 98 (08) :1457-1466
[4]   BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families [J].
Antoniou, AC ;
Durocher, F ;
Smith, P ;
Simard, J ;
Easton, DF .
BREAST CANCER RESEARCH, 2006, 8 (01)
[5]   The BOADICEA model of genetic susceptibility to breast and ovarian cancer [J].
Antoniou, AC ;
Pharoah, PPD ;
Smith, P ;
Easton, DF .
BRITISH JOURNAL OF CANCER, 2004, 91 (08) :1580-1590
[6]   Validation study of the LAMBDA model for predicting the BRCA1 or BRCA2 mutation carrier status of North American Ashkenazi Jewish women [J].
Apicella, C. ;
Dowty, J. G. ;
Dite, G. S. ;
Jenkins, M. A. ;
Senle, R. T. ;
Daly, M. B. ;
Andrulis, I. L. ;
John, E. M. ;
Buys, S. S. ;
Li, F. P. ;
Glendon, G. ;
Chung, W. ;
Ozcelik, H. ;
Miron, A. ;
Kotar, K. ;
Southey, M. C. ;
Foulkes, W. D. ;
Hopper, J. L. .
CLINICAL GENETICS, 2007, 72 (02) :87-97
[7]   Assessing BRCA carrier probabilities in extended families [J].
Barcenas, CH ;
Hosain, GMM ;
Arun, B ;
Zong, JH ;
Zhou, XJ ;
Chen, JF ;
Cortada, JM ;
Mills, GB ;
Tomlinson, GE ;
Miller, AR ;
Strong, LC ;
Amos, CI .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (03) :354-360
[8]   BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes [J].
Berry, DA ;
Iversen, ES ;
Gudbjartsson, DF ;
Hiller, EH ;
Garber, JE ;
Peshkin, BN ;
Lerman, C ;
Watson, P ;
Lynch, HT ;
Hilsenbeck, SG ;
Rubinstein, WS ;
Hughes, KS ;
Parmigiani, G .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (11) :2701-2712
[9]   Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history [J].
Berry, DA ;
Parmigiani, G ;
Sanchez, J ;
Schildkraut, J ;
Winer, E .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (03) :227-238
[10]   Improving the accuracy of BRCA1/2 mutation prediction: validation of the novel country-customized IC software [J].
Capalbo, C ;
Ricevuto, E ;
Vestri, A ;
Sidoni, T ;
Buffone, A ;
Cortesi, E ;
Marchetti, P ;
Scambia, G ;
Tomao, S ;
Rinaldi, C ;
Zani, M ;
Ferraro, S ;
Frati, L ;
Screpanti, I ;
Gulino, A ;
Giannini, G .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (01) :49-54