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lüll Cancer treatment-induced bone loss: pathophysiology and clinical perspectives Brufsky AMOncologist 2008[Feb]; 13 (2): 187-95Hormone-ablative therapies for breast or prostate cancer can cause marked and rapid reductions in circulating estrogen or testosterone levels, resulting in significant effects on bone metabolism and cancer treatment-induced bone loss (CTIBL). Most patients with cancer are over the age of 65 and are already at risk for osteoporosis. Thus, accelerated bone loss from CTIBL is especially concerning in this population. Although there are currently no approved therapies for the treatment or prevention of CTIBL, oral bisphosphonates have been used in settings other than oncology to treat bone loss. New-generation i.v. bisphosphonates have demonstrated promising activity in preventing CTIBL in patients receiving hormonal therapy for breast or prostate cancer. In particular, zoledronic acid not only prevents CTIBL in both breast and prostate cancer patients but also increases bone mineral density above baseline. Such agents have the potential to delay or prevent CTIBL in patients receiving hormonal therapies.|Aged[MESH]|Antineoplastic Agents, Hormonal/administration & dosage/*adverse effects[MESH]|Aromatase Inhibitors/adverse effects[MESH]|Bone Density Conservation Agents/therapeutic use[MESH]|Bone Resorption/chemically induced/*physiopathology/*prevention & control[MESH]|Breast Neoplasms/*drug therapy[MESH]|Diphosphonates/therapeutic use[MESH]|Female[MESH]|Humans[MESH]|Imidazoles/therapeutic use[MESH]|Male[MESH]|Osteoporosis/prevention & control[MESH]|Prostatic Neoplasms/*drug therapy[MESH]|Zoledronic Acid[MESH] |