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Long-term raloxifene for postmenopausal osteoporosis.
Robert R Recker1, Bruce H Mitlak, Xiao Ni
1Osteoporosis Research Center, Creighton University, Omaha, NE, USA.
Current Medical Research and Opinion
|July 27, 2011
Summary
Long-term raloxifene use for osteoporosis effectively reduces fracture risk and invasive breast cancer incidence. Bone mineral density is preserved, and bone turnover markers normalize with sustained treatment.
Area of Science:
- Pharmacology
- Bone Biology
- Oncology
Background:
- Osteoporosis and invasive breast cancer are chronic conditions requiring long-term treatment.
- Raloxifene 60 mg/day is indicated for extended osteoporosis management (over 3 years).
Purpose of the Study:
- To evaluate the long-term efficacy and safety of raloxifene therapy.
- To assess raloxifene's impact on fracture risk, bone mineral density, bone turnover, and invasive breast cancer incidence over extended periods.
Main Methods:
- Review of available data on long-term raloxifene use.
- New analyses and data from iliac crest bone biopsies after 8 years of raloxifene therapy.
- Key studies included the Multiple Outcomes of Raloxifene Evaluation (MORE) and Continued Outcomes of Raloxifene Evaluation (CORE).
Main Results:
- Raloxifene demonstrated sustained vertebral fracture risk reduction over 4 years, with similar risk reduction in the fourth year compared to years 0-3.
- Continued treatment preserved bone mineral density (BMD) and lowered bone turnover markers to premenopausal levels.
- Eight-year bone biopsies showed normal bone histology and cellular activity.
- Raloxifene significantly reduced invasive breast cancer risk, with benefits increasing with treatment duration up to 8 years.
Conclusions:
- Long-term raloxifene therapy is effective in reducing fracture risk and invasive breast cancer incidence.
- Sustained raloxifene use maintains BMD and bone quality.
- The benefits of raloxifene in reducing invasive breast cancer risk are duration-dependent.
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