Accounting for individualized competing mortality risks in estimating postmenopausal breast cancer risk

被引:7
|
作者
Schonberg, Mara A. [1 ,7 ]
Li, Vicky W. [1 ]
Eliassen, A. Heather [2 ,3 ]
Davis, Roger B. [1 ]
LaCroix, Andrea Z. [4 ]
McCarthy, Ellen P. [1 ]
Rosner, Bernard A. [2 ,3 ]
Chlebowski, Rowan T. [5 ]
Hankinson, Susan E. [2 ,3 ,6 ]
Marcantonio, Edward R. [1 ]
Ngo, Long H. [1 ]
机构
[1] Harvard Med Sch, Div Gen Med & Primary Care, Dept Med, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[3] Harvard Med Sch, Brigham & Womens Hosp, Channing Div Network Med, Boston, MA USA
[4] Univ Calif San Diego, Div Epidemiol Family Med & Publ Hlth, La Jolla, CA 92093 USA
[5] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Torrance, CA 90509 USA
[6] Univ Massachusetts, Dept Biostat & Epidemiol, 713 North Pleasant St, Amherst, MA 01003 USA
[7] Beth Israel Deaconess Med Ctr, 1309 Beacon,Off 219, Brookline, MA 02446 USA
基金
美国国家卫生研究院;
关键词
Breast cancer prediction; Competing risks; Older; OLDER-ADULTS; PROSPECTIVE COHORT; HORMONE-THERAPY; WOMEN; MODEL; VALIDATION; DENSITY; INDEX; PROBABILITIES; INFORMATION;
D O I
10.1007/s10549-016-4020-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accurate risk assessment is necessary for decision-making around breast cancer prevention. We aimed to develop a breast cancer prediction model for postmenopausal women that would take into account their individualized competing risk of non-breast cancer death. We included 73,066 women who completed the 2004 Nurses' Health Study (NHS) questionnaire (all aeyen57 years) and followed participants until May 2014. We considered 17 breast cancer risk factors (health behaviors, demographics, family history, reproductive factors) and 7 risk factors for non-breast cancer death (comorbidities, functional dependency) and mammography use. We used competing risk regression to identify factors independently associated with breast cancer. We validated the final model by examining calibration (expected-to-observed ratio of breast cancer incidence, E/O) and discrimination (c-statistic) using 74,887 subjects from the Women's Health Initiative Extension Study (WHI-ES; all were aeyen55 years and followed for 5 years). Within 5 years, 1.8 % of NHS participants were diagnosed with breast cancer (vs. 2.0 % in WHI-ES, p = 0.02), and 6.6 % experienced non-breast cancer death (vs. 5.2 % in WHI-ES, p < 0.001). Using a model selection procedure which incorporated the Akaike Information Criterion, c-statistic, statistical significance, and clinical judgement, our final model included 9 breast cancer risk factors, 5 comorbidities, functional dependency, and mammography use. The model's c-statistic was 0.61 (95 % CI [0.60-0.63]) in NHS and 0.57 (0.55-0.58) in WHI-ES. On average, our model under predicted breast cancer in WHI-ES (E/O 0.92 [0.88-0.97]). We developed a novel prediction model that factors in postmenopausal women's individualized competing risks of non-breast cancer death when estimating breast cancer risk.
引用
收藏
页码:547 / 562
页数:16
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