Effect of raloxifene on bone mineral density in premenopausal women at increased risk of breast cancer

被引:26
作者
Eng-Wong, J.
Reynolds, J. C.
Venzon, D.
Liewehr, D.
Gantz, S.
Danforth, D.
Liu, E. T.
Chow, C.
Zujewski, J.
机构
[1] NCI, Med Oncol Clin Res Unit, NIH, Bethesda, MD 20892 USA
[2] NCI, Surg Oncol Branch, NIH, Bethesda, MD 20892 USA
[3] NIH, Ctr Clin, Bethesda, MD 20892 USA
[4] Genome Inst Singapore, Singapore 138672, Singapore
关键词
D O I
10.1210/jc.2005-2827
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Raloxifene is a promising breast cancer prevention agent in postmenopausal women at increased risk for breast cancer. The effects of raloxifene in premenopausal women are unknown. Objective: We evaluated the effect of raloxifene in premenopausal women at increased risk for breast cancer on bone mineral density (BMD). Design: This was a phase II clinical trial. Setting: This study was conducted at an academic medical center. Participants: Thirty-seven premenopausal women at increased risk for breast cancer enrolled in the trial. Thirty subjects began treatment and 27 were evaluable. Intervention: Raloxifene ( 60 mg daily) and elemental calcium ( 500 mg daily) were given for 2 yr. Subjects were followed up off medications for 1 yr. Main Outcome Measure: The primary end point was the intra-subject percent change in BMD at 1 yr measured by dual-energy x-ray absorptiometry. Results: The mean baseline lumbar spine density was 1.027 g/cm(2). Lumbar spine density decreased 2.3% at 1 yr ( P < 0.00001) and 3.5% at 2 yr ( P < .00001). Percent change from yr 2 to 3 was +1.4%. The mean baseline total hip bone density was 0.905 g/cm(2). Total hip density decreased 0.3% at 1 yr and 1.0% at 2 yr ( P = 0.033). Percent change from yr 2 to 3 was + 1.7%. Conclusions: Raloxifene use is associated with a decrease in BMD in premenopausal women at increased risk for breast cancer. The clinical significance of this decrease is unknown and is attenuated with stopping raloxifene.
引用
收藏
页码:3941 / 3946
页数:6
相关论文
共 34 条
[31]   The selective estrogen receptor modulator raloxifene regulates osteoclast and osteoblast activity in vitro [J].
Taranta, A ;
Brama, M ;
Teti, A ;
De Luca, V ;
Scandurra, R ;
Spera, G ;
Agnusdei, D ;
Termine, JD ;
Migliaccio, S .
BONE, 2002, 30 (02) :368-376
[32]   Effects of tamoxifen vs raloxifene on the risk of developing invasive breast cancer and other disease outcomes - The NSABP study of tamoxifen and raloxifene (STAR) P-2 trial [J].
Vogel, Victor G. ;
Costantino, Joseph P. ;
Wickerham, D. Lawrence ;
Cronin, Walter M. ;
Cecchini, Reena S. ;
Atkins, James N. ;
Bevers, Therese B. ;
Fehrenbacher, Louis ;
Pajon, Eduardo R., Jr. ;
Wade, James L., III ;
Robidoux, Andre ;
Margolese, Richard G. ;
James, Joan ;
Lippman, Scott M. ;
Runowicz, Carolyn D. ;
Ganz, Patricia A. ;
Reis, Steven E. ;
McCaskill-Stevens, Worta ;
Ford, Leslie G. ;
Jordan, V. Craig ;
Wolmark, Norman .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (23) :2727-2741
[33]   The effects of hormone replacement therapy and raloxifene on C-reactive protein and homocysteine in healthy postmenopausal women: A randomized, controlled trial [J].
Walsh, BW ;
Paul, S ;
Wild, RA ;
Dean, RA ;
Tracy, RP ;
Cox, DA ;
Anderson, PW .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (01) :214-218
[34]  
WARE JE, 2002, SF36 HLTH SURV MAN I