Prior hormone therapy and breast cancer risk in the Women's Health initiative randomized trial of estrogen plus progestin

被引:175
作者
Anderson, Garnet L.
Chlebowski, Rowan T.
Rossouw, Jacques E.
Rodabough, Rebecca J.
McTiernan, Anne
Margolis, Karen L.
Aggerwal, Anita
Curb, J. David
Hendrix, Susan L.
Hubbell, F. Allan
Khandekar, Jamardan
Lane, Dorothy S.
Lasser, Norman
Lopez, Ana Maria
Potter, JoNell
Ritenbaugh, Cheryl
机构
[1] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, WHI Clin Coordinating Ctr, Seattle, WA 98109 USA
[2] NHLBI, WHI, Rockville, MD USA
[3] Univ Calif Los Angeles, Ctr Med, LABiomed, Los Angeles Biomed Res Inst Harbor, Torrance, CA USA
[4] Hennepin Cty Med Ctr, Berman Ctr Clin Res, Minneapolis, MN 55415 USA
[5] Washington Hosp Ctr, Washington, DC 20010 USA
[6] Univ Hawaii, John A Burns Sch Med, Dept Geriatr Med, Honolulu, HI 96822 USA
[7] Wayne State Univ, Sch Med, Hutzel Womens Hosp, Dept Obstet & Gynecol, Detroit, MI USA
[8] Univ Calif Irvine, Dept Med, Irvine, CA 92717 USA
[9] Northwestern Univ, Dept Med, Evanston, IL USA
[10] SUNY Stony Brook, Stony Brook, NY 11794 USA
[11] Univ Med & Dent New Jersey, Newark, NJ 07103 USA
[12] Univ Arizona, Tucson, AZ USA
[13] Univ Miami, Miami, FL 33152 USA
关键词
estrogen; progestin; breast neoplasms; subgroup analyses; randomized trials;
D O I
10.1016/j.maturitas.2006.05.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objectives: To assess the extent to which prior hormone therapy modifies the breast cancer risk found with estrogen plus progestin (E+P) in the Women's Health Initiative (WHI) randomized trial. Methods: Subgroup analyses of prior hormone use on invasive breast cancer incidence in 16,608 postmenopausal women in the WHI randomized trial of E+P over an average 5.6 years of follow-up. Results: Small but statistically significant differences were found between prior HT users and non-users for most breast cancer risk factors but Gail risk scores were similar. Duration of E + P use within the trial (mean 4.4 years, S.D. 2.0) did not vary by prior use. Among 4311 prior users, the adjusted hazard ratio (HR) for E+P versus placebo was 1.96 (95% confidence interval [CI]: 1.17-3.27), significantly different (p=0.03) from that among 12,297 never users (HR 1.02; 95% CI: 0.77-1.36). The interaction between study arm and follow-up time was significant overall (p=0.01) and among never users (p=0.02) but not among prior users (p=0.10). The cumulative incidence over time for the E+P and placebo groups appeared to cross after about 3 years in prior users, and after about 5 years in women with no prior use. No interaction was found with duration (p=0.08) or recency of prior use (p=0.17). Prior hormone use significantly increased the E+P hazard ratio for larger, more advanced tumors. Conclusion: A safe interval for combined hormone use could not be reliably defined with these data. However, the significant increase in breast cancer risk in the trial overall after only 5.6 years of follow-up, initially concentrated in women with prior hormone exposure, but with increasing risk over time in women without prior exposure, suggests that durations only slightly longer than those in the WHI trial are associated with increased risk of breast cancer. Longer-term exposure and follow-up data are needed. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:103 / 115
页数:13
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