Zoledronic acid for treatment of osteopenia and osteoporosis in women with primary breast cancer undergoing adjuvant aromatase inhibitor therapy☆☆☆
Abstract
Background
Postmenopausal women with osteoporosis/osteopenia are at increased risk of fracture. Aromatase inhibitors further increase bone loss in these patients. This study evaluates whether zoledronic acid prevents the bone loss expected when these patients initiate letrozole.
Patients and methods
Postmenopausal women with estrogen and/or progesterone receptor-positive breast cancer and a bone mineral density (BMD) T-score <−2.0 were given letrozole 2.5
mg/vitamin D 400 international units daily, calcium 500
mg twice daily, and 4
mg zoledronic acid every 6
months. The BMD was assessed at baseline and 1
year. The primary endpoint was the mean change in lumbar spine (LS) BMD at 1
year.
Results
Forty-six patients completed 1
year of treatment. LS BMD increased by 2.66% (p
=
0.01), femoral neck (FN) by 4.81% (p
=
0.01), and any measured endpoint by 4.55% (p
=
0.0052).
Conclusions
Zoledronic acid prevents bone loss in postmenopausal women with osteoporosis/osteopenia starting letrozole and is associated with improvements in BMD.
Keywords: Breast cancer, Osteoporosis, Aromatase inhibitors
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☆ This study was conducted as a trial of the Mayo Cancer Center Research Consortium in part by Public Health Service grants CA-35431, CA-35195, and CA-52352. The content is solely the responsibility of the authors and does not necessarily represent the views of the National Cancer Institute or the National Institute of Health.
☆☆ Additional participating institutions include: Carle Cancer Center CCOP, Urbana, IL 61801 (Kendrith M. Rowland, Jr.); Cedar Rapids Oncology Project CCOP, Cedar Rapids, IA 52403 (Martin Wiesenfeld).
PII: S0960-9776(09)00173-8
doi:10.1016/j.breast.2009.12.001
© 2009 Elsevier Ltd. All rights reserved.
