T. Powles et al., EFFECT OF TAMOXIFEN ON BONE-MINERAL DENSITY MEASURED BY DUAL-ENERGY X-RAY ABSORPTIOMETRY IN HEALTHY PREMENOPAUSAL AND POSTMENOPAUSAL WOMEN, Journal of clinical oncology, 14(1), 1996, pp. 78-84
Purpose: Tamoxifen is an effective treatment for metastatic and primar
y breast cancer and is now being evaluated as a chemoprevention agent
in healthy women. Any long-term effects on estrogen-sensitive tissues
such as bone may have important therapeutic implications. Methods: We
measured bone mineral density (BMD) in the lumbar spine and hip using
dual-energy x-ray absorptiometry (DXA) in premenopausal and postmenopa
usal healthy women who participated in our placebo-controlled tamoxife
n chemoprevention of breast cancer trial. Results: BMD delta are now a
vailable from 179 women for this analysis. In premenopausal women, BMD
decreased progressively in the lumbar spine (P <.001) and in the hip
(P <.05) for women on tamoxifen, but not those on placebo. The mean an
nual loss in lumbar BMD per year over the 3-year study period in tamox
ifen-treated compliant women who remained premenopausal throughout the
study period was 1.44% (1.88% calculated on an intent-to-treat basis)
compared with a small gain of 0.24% per annum for women on placebo (P
< .001). Tamoxifen had the opposite effect in postmenopausal women. T
he mean annual increase in BMD for women on tamoxifen was 1.17% in the
spine (P <.005) and 1.71% in the hip (P <.001) compared with a nonins
ignificant loss for women on placebo. Conclusion: These results indica
te that tamoxifen treatment is associated with a significant loss of B
MD in premenopausal women, whereas it prevents bone loss in postmenopa
usal women. These adverse and beneficial effects of tamoxifen should b
e considered in the assessment of the therapeutic benefits for both th
e adjuvant treatment and the chemoprevention of breast cancer. (C) 199
6 by American Society of Clinical Oncology.