Hormone replacement therapy regimens and breast cancer risk

被引:149
作者
Weiss, LK
Burkman, RT
Cushing-Haugen, KL
Voigt, LF
Simon, MS
Daling, JR
Norman, SA
Bernstein, L
Ursin, G
Marchbanks, PA
Strom, BL
Berlin, JA
Weber, AL
Doody, DR
Wingo, PA
McDonald, JA
Malone, KE
Folger, SG
Spirtas, R
机构
[1] Wayne State Univ, Populat Studies & Prevent Program, Karmanos Canc Inst, Detroit, MI USA
[2] Henry Ford Hlth Syst, Dept Obstet & Gynecol, Detroit, MI USA
[3] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[4] Wayne State Univ, Karmanos Canc Inst, Dept Internal Med, Detroit, MI USA
[5] Univ Penn, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[7] Univ So Calif, Dept Prevent Med, Los Angeles, CA 90089 USA
[8] Ctr Dis Control & Prevent, Div Reprod Hlth, Atlanta, GA USA
[9] Ctr Dis Control & Prevent, Div Canc Prevent & Control, Atlanta, GA USA
[10] NICHHD, Contracept & Reprod Hlth Branch, Populat Res Ctr, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S0029-7844(02)02502-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Hormone replacement therapy (HRT) has increased in the United States over the past 2 decades in response to reports of long-term health benefits. A relationship between HRT and breast cancer risk has been observed in a number of epidemiological studies. In 2002, the Women's Health Initiative Randomized Controlled Trial reported an association between continuous combined HRT and breast cancer risk. The objective of this study was to examine die association between breast cancer risk and HRT according to regimen and duration and recency of use. METHODS: A multicenter, population-based, case-control study was conducted in five United States metropolitan areas from 1994 to 1998. Analyzed were data from 3823 postmenopausal white and black women (1,870 cases and 1953 con-trols) aged 35-64 years. Odds ratios (ORs) were calculated as estimates of breast cancer risk using standard, unconditional, multivariable logistic regression analysis. Potential confounders were included in the final model if they altered ORs by 10% or more. Two-sided P values for trend were computed from the likelihood ratio statistic. RESULTS: Continuous combined HRT was associated with increased breast cancer risk among current users of 5 or more years (1.54; 95% confidence interval 1.10, 2.17). Additionally, a statistically significant trend indicating increasing breast cancer risk with longer duration of continuous combined HRT was observed among current users (P=.01). There were no positive associations between breast cancer risk and other HRT regimens. CONCLUSION: Our data suggest a positive association between continuous combined HRT and breast cancer risk among current, longer term users. Progestin administered in an uninterrupted regimen may be a contributing factor. Risk dissipates once use is discontinued. (C) 2002 by The American College of Obstetricians and Gynecologists.
引用
收藏
页码:1148 / 1158
页数:11
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