Type and duration of exogenous hormone use affects breast cancer histology

被引:13
|
作者
Kumar, Anjali S.
Cureton, Elizabeth
Shim, Veronica
Sakata, Theadora
Moore, Dan H.
Benz, Christopher C.
Esserman, Laura J.
Hwang, E. Shelley [1 ]
机构
[1] Univ Calif San Francisco, Ctr Comprehens Canc, Dept Surg, San Francisco, CA 94143 USA
[2] Kaiser Permanente Oakland Med Ctr, Dept Surg, Oakland, CA 94602 USA
[3] Univ Calif San Francisco E Bay, Dept Surg, Oakland, CA 94602 USA
[4] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Med, Div Hematol & Oncol, San Francisco, CA 94143 USA
[6] Buck Inst Age Res, Novato, CA 94945 USA
关键词
breast cancer; hormone replacement therapy; estrogen receptor;
D O I
10.1245/s10434-006-9129-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: It is unclear whether hormone replacement therapy (HRT), in addition to increasing risk for breast cancer, affects the type of breast cancer diagnosed. We conducted this investigation to assess whether the type of hormone used (none, estrogen, progesterone, or combined) and duration of use influences subsequent breast cancer histology. Methods: We performed a retrospective cohort analysis among women listed as incident cases of breast malignancy in the Kaiser Permanente Northern California Cancer Registry during 2003 (n = 2830). Type and duration of hormone used (none, estrogen, progesterone, or combined) before breast cancer diagnosis was obtained from electronic pharmacy records. The association between type and duration of hormone use with characteristics of subsequent breast cancers was examined. Results: Among women aged >50 years (n = 1701), any use of estrogen, progesterone, or combination therapy was not associated with an increased risk of estrogen receptor (ER)-positive disease. However, >6 months' use of combined HRT increased the odds of ER-positive tumors (odds ratio, 1.65; 95% confidence interval, 1.07-2.5; P = .02). Estrogen HRT patients were more likely than nonusers to present with low-grade (P = .05), and early-stage tumors (P = .03). This trend was not seen in combined HRT users. Conclusions: Short-duration HRT did not increase the likelihood of ER-positive breast cancer. However, prolonged duration of combined HRT, but not estrogen or progesterone alone, resulted in a marked increase in ER-positive disease. Our findings suggest that the effect of combined HRT on breast cancer incidence or progression is not immediate and that long-term use is more likely to affect breast cancer histology.
引用
收藏
页码:695 / 703
页数:9
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