The use of bisphosphonates in patients with breast cancer Journal Article


Author: Van Poznak, C. H.
Article Title: The use of bisphosphonates in patients with breast cancer
Abstract: Background: Bone is the most common site of breast cancer metastases. Skeletal metastases may be associated with harmful and painful events such as fractures, spinal cord compression, and hypercalcemia. By inhibiting osteoclasts and bone resorption, bisphosphonates can interrupt the process of bone destruction and decrease the risk of skeletal complications. Methods: A review of the literature was undertaken regarding the use of bisphosphonates in breast cancer management, with particular attention to prospective, randomized clinical trials that have influenced the treatment of bone metastases. Results: Large prospective, randomized trials have demonstrated that bisphosphonates are effective in reducing skeletal-related complications from metastatic breast cancer. Conclusions: For many patients with osseous lesions from breast cancer, bisphosphonate therapy is a useful intervention in managing their disease. Bisphosphonates are the treatment of choice for hypercalcemia of malignancy and bisphosphonates reduce the risk of pathologic fractures, spinal cord compromise, the need for radiation or surgery to bone, and bone pain.
Keywords: bone neoplasms; osteolysis; review; bone metastasis; pathophysiology; paclitaxel; cancer radiotherapy; chemotherapy, adjuvant; cancer incidence; cancer palliative therapy; palliative care; multiple myeloma; breast cancer; bisphosphonic acid derivative; bone pain; hypercalcemia; practice guideline; antineoplastic activity; breast neoplasms; risk factor; risk assessment; spinal cord compression; osteoclast; osteoporosis; guidelines; infusions, intravenous; diphosphonates; zoledronic acid; bone destruction; imidazoles; osteopenia; pamidronic acid; pathologic fracture; humans; human; female; pharmacoeconomics
Journal Title: Cancer Control
Volume: 9
Issue: 6
ISSN: 1073-2748
Publisher: H. Lee Moffitt Cancer Center & Research Institute  
Date Published: 2002-01-01
Start Page: 480
End Page: 489
Language: English
PUBMED: 12514566
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 14 November 2014 -- Source: Scopus
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