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Article Summary

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Risedronate prevents bone loss in breast cancer survivors: A 2-year, randomized, double-blind, placebo-controlled clinical trial
Journal of Clinical Oncology, 06/17/08
Print     Email This Article     Save in My Library   Free Abstract
Greenspan SL et al. - In postmenopausal women with breast cancer with or without aromatase inhibitor (AI) therapy, once-weekly oral risedronate was beneficial for spine and hip bone mineral density (BMD), reduced bone turnover, and was well tolerated.

Methods
  • Study to examine prevention of breast cancer–related bone loss
  • 87 postmenopausal women after chemotherapy for BCa were randomly assigned to once-weekly risedronate 35 mg or placebo for 24 mos
  • Outcomes included BMD and turnover markers

Results
  • At study initiation, 13% of pts were on an AI
  • After 24 mos, there were differences of 1.6 to 2.5% at the spine and hip BMD between the placebo and risedronate groups
  • At study completion, 44% were on an AI
  • Adjusting for an AI, women on placebo plus AI had a decrease in BMD of 4.8% ± 0.8% at the spine and 2.8% ± 0.5% at the total hip
  • In women on risedronate + AI, the spine decreased by 2.4% ± 1.1% and was stable at the hip
  • Women in the placebo group not on an AI, maintained BMD at the spine, and had a 1.2% ± 0.5% loss at the total hip
  • Women who received risedronate but no AI had the greatest improvement in BMD of 2.2% ± 0.9% at the total hip
  • Bone turnover was reduced with risedronate
  • There were no differences in adverse events between the groups

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