Sex hormones, risk factors, and risk of estrogen receptor-positive breast cancer in older women: A long-term prospective study

被引:58
作者
Cummings, SR
Lee, JS
Lui, LY
Stone, K
Ljung, BM
Cauleys, JA
机构
[1] Calif Pacific Med Ctr, Res Inst, Coordinating Ctr, San Francisco, CA 94105 USA
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[3] Univ Pittsburgh, Dept Epidemiol, Pittsburgh, PA 15261 USA
关键词
D O I
10.1158/1055-9965.EPI-04-0375
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objective: Antiestrogens reduce the risk of estrogen receptor-positive (ER+) but not ER-negative (ER-) breast cancer. Women at high risk of ER+ cancer would be the most likely to benefit from these treatments, but the best approach to predicting ER+ cancer is uncertain. Methods: We prospectively assessed putative risk factors for breast cancer and archived serum at -190 degrees C from a community-based cohort of 7,676 women ages >= 65 years who had no history of breast cancer. Follow-up for breast cancer over 10.5 years was 99% complete. Using a case-cohort design, we measured baseline levels of estradiol and testosterone in 196 cases of invasive ER+ cancer and 378 randomly selected controls. Results: Women whose testosterone level in highest two quintiles had a 4-fold increased risk of ER+ breast cancer (P < 0.0001). High estradiol concentration also indicated an increased risk but was not a significant predictor after adjustment for testosterone. Women with > 16 years of education had a 2.1 times increased risk (P = 0.03) of ER+ cancer, but no other risk factors were significantly related to an increased risk of ER+ cancer. Women with a family history of breast cancer had a 2.9-fold increased risk of ER- cancer (P = 0.002) but no increased risk of ER+ cancer (relative hazard = 1.2, 0.8-1.8). Conclusions: High serum testosterone and advanced education predicted ER+ breast cancer. If confirmed, high testosterone level may be more accurate than family history of breast cancer and other conventional risk factors for identifying older women who are most likely to benefit from antiestrogen chemoprevention.
引用
收藏
页码:1047 / 1051
页数:5
相关论文
共 36 条
[1]
Baum M, 2002, LANCET, V359, P2131
[2]
Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50 302 women with breast cancer and 96 973 women without the disease [J].
Beral, V ;
Bull, D ;
Doll, R ;
Peto, R ;
Reeves, G ;
La Vecchia, C ;
Magnusson, C ;
Miller, T ;
Peterson, B ;
Pike, M ;
Thomas, D ;
van Leeuwen, F .
LANCET, 2002, 360 (9328) :187-195
[3]
CARTER CL, 1989, PUBLIC HEALTH REP, V104, P45
[4]
Bone mineral density and risk of breast cancer in older women - The study of osteoporotic fractures [J].
Cauley, JA ;
Lucas, FL ;
Kuller, LH ;
Vogt, MT ;
Browner, WS ;
Cummings, SR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (17) :1404-1408
[5]
Elevated serum estradiol and testosterone concentrations are associated with a high risk for breast cancer [J].
Cauley, JA ;
Lucas, FL ;
Kuller, LH ;
Stone, K ;
Browner, W ;
Cummings, SR .
ANNALS OF INTERNAL MEDICINE, 1999, 130 (04) :270-+
[6]
Risk factors for breast cancer according to estrogen and progesterone receptor status [J].
Colditz, GA ;
Rosner, BA ;
Chen, WY ;
Holmes, MD ;
Hankinson, SE .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (03) :218-228
[7]
Cotterchio M, 2003, CANCER EPIDEM BIOMAR, V12, P1053
[8]
The effect of raloxifene on risk of breast cancer in postmenopausal women - Results from the MORE randomized trial [J].
Cummings, SR ;
Eckert, S ;
Krueger, KA ;
Grady, D ;
Powles, TJ ;
Cauley, JA ;
Norton, L ;
Nickelsen, T ;
Bjarnason, NH ;
Morrow, M ;
Lippman, ME ;
Black, D ;
Glusman, JE ;
Costa, A ;
Jordan, VC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (23) :2189-2197
[9]
Serum estradiol level and risk of breast cancer during treatment with raloxifene [J].
Cummings, SR ;
Duong, T ;
Kenyon, E ;
Cauley, JA ;
Whitehead, M ;
Krueger, KA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (02) :216-220
[10]
Overview of the main outcomes in breast-cancer prevention trials [J].
Cuzick, J ;
Powles, T ;
Veronesi, U ;
Forbes, J ;
Edwards, R ;
Ashley, S ;
Boyle, P .
LANCET, 2003, 361 (9354) :296-300