Estimates of the number of US women who could benefit from tamoxifen for breast cancer chemoprevention

被引:182
作者
Freedman, AN
Graubard, BI
Rao, SR
McCaskill-Stevens, W
Ballard-Barbash, R
Gail, MH
机构
[1] NCI, Div Canc Control & Populat Sci, Bethesda, MD 20892 USA
[2] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[3] NCI, Div Canc Prevent, Bethesda, MD 20892 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2003年 / 95卷 / 07期
关键词
D O I
10.1093/jnci/95.7.526
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The Breast Cancer Prevention Trial demonstrated that tamoxifen treatment produced a 49% reduction in the risk of invasive breast cancer among women at elevated risk for the disease. The U.S. Food and Drug Administration (FDA) subsequently approved tamoxifen for women aged 35 years or older with a 5-year breast cancer risk of 1.67% or higher for breast cancer chemoprevention. However, tamoxifen use has been associated with adverse outcomes, and not all eligible women have a positive benefit/risk ratio. Methods: We used weighted data from the year 2000 National Health Interview Survey Cancer Control Module to estimate the total number of U.S. women, aged 35-79 years, who were eligible for tamoxifen chemoprevention based on the FDA eligibility criteria. We also estimated the numbers of white and black women who would benefit from tamoxifen chemoprevention on the basis of a positive benefit/risk index developed by Gail et al. Results: Of the 65826074 women aged 35-79 years without reported breast cancer in the United States in 2000, 10232816 women (15.5%, 95% confidence interval [CI] = 14.7% to 16.3%) would be eligible for tamoxifen chemoprevention. The percentage of U.S. women who would be eligible varied dramatically by race, with 18.7% (95% CI = 17.8% to 19.7%) of white women, 5.7% (95% CI = 4.3% to 7.5%) of black women, and 2.9% (95% CI = 2.1% to 3.9%) of Hispanic women being eligible. Of the 50 104 829 white U.S. women aged 3579 years, 2431911 (4.9%, 95% CI = 4.3% to 5.4%) would have a positive benefit/risk index for tamoxifen chemoprevention. Of the 7481779 black U.S. women aged 35-79 years, only 42768 (0.6%, 95% CI = 0.2% to 1.3%) would have a positive benefit/risk index. Among white women, 28492 (95% CI = 24693 to 32292) breast cancers would be prevented or deferred if those women who have a positive net benefit index took tamoxifen over the next 5 years. Conclusion: A substantial percentage of U.S. women would be eligible for tamoxifen chemoprevention according to FDA criteria, but a much smaller percentage would have an estimated net benefit. Nevertheless, this latter percentage corresponds to more than two million women. [J Natl Cancer Inst 2003;95:526-32]
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页码:526 / 532
页数:7
相关论文
共 18 条
[1]  
[Anonymous], NSABP BREAST CANC PR
[2]  
BOTMAN SL, 2000, NATL VITAL STAT REP, P1
[3]   Validation studies for models projecting the risk of invasive and total breast cancer incidence [J].
Costantino, JP ;
Gail, MH ;
Pee, D ;
Anderson, S ;
Redmond, CK ;
Benichou, J ;
Wieand, HS .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (18) :1541-1548
[4]  
Cuzick J, 2002, LANCET, V360, P817
[5]   Tamoxifen for prevention of breast cancer: Report of the National Surgical Adjuvant Breast and Bowel Project P-1 study [J].
Fisher, B ;
Costantino, JP ;
Wickerham, DL ;
Redmond, CK ;
Kavanah, M ;
Cronin, WM ;
Vogel, V ;
Robidoux, A ;
Dimitrov, N ;
Atkins, J ;
Daly, M ;
Wieand, S ;
Tan-Chiu, E ;
Ford, L ;
Wolmark, N .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (18) :1371-1388
[6]   National surgical adjuvant breast and bowel project breast cancer prevention trial: A reflective commentary [J].
Fisher, B .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (05) :1632-1639
[7]   PROJECTING INDIVIDUALIZED PROBABILITIES OF DEVELOPING BREAST-CANCER FOR WHITE FEMALES WHO ARE BEING EXAMINED ANNUALLY [J].
GAIL, MH ;
BRINTON, LA ;
BYAR, DP ;
CORLE, DK ;
GREEN, SB ;
SCHAIRER, C ;
MULVIHILL, JJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (24) :1879-1886
[8]   Weighing the risks and benefits of tamoxifen treatment for preventing breast cancer [J].
Gail, MH ;
Costantino, JP ;
Bryant, J ;
Croyle, R ;
Freedman, L ;
Helzlsouer, K ;
Vogel, V .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (21) :1829-1846
[9]  
Korn EL, 1999, WILEY S PRO STAT SUR
[10]  
NEWMAN LA, 2002, P ASCO, V21, pA245