Gail model for prediction of absolute risk of invasive breast cancer: Independent evaluation in the Florence-European Prospective Investigation Into Cancer and Nutrition Cohort

被引:73
作者
Decarli, Adriano
Calza, Stefano
Masala, Giovanna
Specchia, Claudia
Palli, Domenico
Gail, Mitchell H.
机构
[1] Univ Milan, Med Stat & Biometry Inst, I-20133 Milan, Italy
[2] Natl Canc Inst, Unit Med Stat & Biometry, Milan, Italy
[3] Univ Brescia, Med Stat & Biometry Sect, Dept Biomed Sci & Biotechnol, Brescia, Italy
[4] Sci Inst Tuscany, Canc Res & Prevent Ctr, Mol & Nutr Epidemiol Unit, Florence, Italy
[5] NCI, Biostat Branch, Div Canc Epidemiol & Genet, Bethesda, MD USA
关键词
D O I
10.1093/jnci/djj463
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. The Gail model 2 (GM) for predicting the absolute risk of invasive breast cancer has been used for counseling and to design intervention studies. Although the GM has been validated in US populations, its performance in other populations is unclear because of the wide variation in international breast cancer rates. Methods: We used data from a multicenter case-control study in Italy and from Italian cancer registries to develop a model (IT-GM) that uses the same risk factors as the GM. We evaluated the accuracy of the IT-GM and the GM using independent data from the Florence-European Prospective Investigation Into Cancer and Nutrition (EPIC) cohort. To assess model calibration (i.e., how well the model predicts the observed numbers of events in subsets of the population), we compared the number of expected incident breast cancers (E) predicted by these models with the number of observed incident breast cancers (0), and we computed the concordance statistic to measure discriminatory accuracy. Results: The overall E/O ratios were 0.96 (95% confidence interval [CI] = 0.84 to 1.11) and 0.93 (95% CI = 0.81 to 1.08) for the IT-GM and the GM, respectively. The IT-GM was somewhat better calibrated than GM in women younger than 50 years, but the GM was better calibrated when age at first live birth categories were considered (e.g., 20- to 24-year age-at-first-birth category E/O = 0.68, 95% CI = 0.53 to 0.94 for the IT-GM and E/O = 0.75, 95% CI = 0.58 to 1.03 for the GM). The concordance statistic was approximately 59% for both models, with 95% confidence intervals indicating that the models perform statistically significantly better than pure chance (concordance statistic of 50%). Conclusions: There was no statistically significant evidence of miscalibration overall for either the IT-GM or the GM, and the models had equivalent discriminatory accuracy. The good performance of the IT-GM when applied on the independent data from the Florence-EPIC cohort indicates that GM can be improved for use in populations other than US populations. Our findings suggest that the Italian data may be useful for revising the GM to include additional risk factors for breast cancer.
引用
收藏
页码:1686 / 1693
页数:8
相关论文
共 41 条
  • [1] Breast cancer risk assessment in indigent women at a public hospital
    Abu-Rustum, NR
    Herbolsheimer, H
    [J]. GYNECOLOGIC ONCOLOGY, 2001, 81 (02) : 287 - 290
  • [2] Global trends in breast cancer incidence and mortality 1973-1997
    Althuis, MD
    Dozier, JM
    Anderson, WF
    Devesa, SS
    Brinton, LA
    [J]. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2005, 34 (02) : 405 - 412
  • [3] Evaluation of breast cancer risk assessment packages in the family history evaluation and screening programme
    Amir, E
    Evans, DG
    Shenton, A
    Lalloo, F
    Moran, A
    Boggis, C
    Wilson, M
    Howell, A
    [J]. JOURNAL OF MEDICAL GENETICS, 2003, 40 (11): : 807 - 814
  • [4] Prospective breast cancer risk prediction model for women undergoing screening mammography
    Barlow, William E.
    White, Emily
    Ballard-Barbash, Rachel
    Vacek, Pamela M.
    Titus-Ernstoff, Linda
    Carney, Patricia A.
    Tice, Jeffrey A.
    Buist, Diana S. M.
    Geller, Berta M.
    Rosenberg, Robert
    Yankaskas, Bonnie C.
    Kerlikowske, Karla
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (17): : 1204 - 1214
  • [5] METHODS OF INFERENCE FOR ESTIMATES OF ABSOLUTE RISK DERIVED FROM POPULATION-BASED CASE-CONTROL STUDIES
    BENICHOU, J
    GAIL, MH
    [J]. BIOMETRICS, 1995, 51 (01) : 182 - 194
  • [6] VARIANCE CALCULATIONS AND CONFIDENCE-INTERVALS FOR ESTIMATES OF THE ATTRIBUTABLE RISK BASED ON LOGISTIC-MODELS
    BENICHOU, J
    GAIL, MH
    [J]. BIOMETRICS, 1990, 46 (04) : 991 - 1003
  • [7] A DELTA METHOD FOR IMPLICITLY DEFINED RANDOM-VARIABLES
    BENICHOU, J
    GAIL, MH
    [J]. AMERICAN STATISTICIAN, 1989, 43 (01) : 41 - 44
  • [8] Bernatsky S, 2003, J RHEUMATOL, V30, P1505
  • [9] Bondy Melissa L., 2003, Cancer, V97, P230, DOI 10.1002/cncr.11018
  • [10] VALIDATION OF A BREAST-CANCER RISK ASSESSMENT MODEL IN WOMEN WITH A POSITIVE FAMILY HISTORY
    BONDY, ML
    LUSTBADER, ED
    HALABI, S
    ROSS, E
    VOGEL, VG
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (08) : 620 - 625