The U.S. Food and Drug Administration (FDA) has expanded the approval of Prolia®  (denosumab) to include treatment of bone loss among breast cancer patients  treated with aromatase inhibitor therapy and prostate cancer patients treated  with androgen deprivation therapy for non-metastatic cancer. Treatment is  intended to increase bone mass among patients at high risk of  fracture.
Osteoporosis affects an estimated 10 million Americans over the age  of 50. Each year, roughly 1.5 million Americans will experience an  osteoporosis-related bone fracture.  These fractures commonly involve the wrist, hip, or spine, but can affect any  part of the body.
Bone loss accelerates as we age (with particularly rapid  loss in women after menopause), but can also be caused by certain types of  cancer treatment. Hormonal therapies such as aromatase inhibitors for breast  cancer and androgen-deprivation therapy for prostate cancer, for example, are  known to cause bone loss. Bone loss from cancer treatment tends to be more rapid  and severe than the bone loss that occurs naturally with aging.
Prolia  targets a protein known as the RANK ligand. This protein regulates the activity  of osteoclasts (cells that break down bone). Prolia has been shown to reduce the  risk of fractures in high-risk postmenopausal women with osteoporosis, and was  approved for this purpose in 2010.
Studies have also now shown that Prolia is  effective against cancer treatment-induced bone loss. In a study of men  undergoing androgen-deprivation therapy for non-metastatic prostate cancer,  those who received Prolia were 62% less likely to develop a new vertebral  fracture than those who received a placebo.Prolia has also been found to improve or maintain bone density among women  undergoing aromatase inhibitor treatment for breast cancer.The most common side effects of Prolia were joint and back pain.
Prolia is  the first drug approved for cancer treatment-induced bone  loss.
References:
  U.S. Department of Health and Human Services. Bone Health and Osteoporosis: A  Report of the Surgeon General. Rockville, MD: U.S. Department of Health and  Human Services, Office of the Surgeon General, 2004.   Body JJ. Prevention and treatment of side-effects of systemic treatment: bone  loss. Annals of Oncology. 2010; 21(supplement 7):vii180-vii185.
Smith MR, Egerdie B, Hernandez Toriz N et al. Denosumab in men receiving  androgen-deprivation therapy for prostate cancer. New England  Journal of Medicine. Early online publication August 11, 2009.
Ellis GK, Bone HG, Chlebowski R et al. Randomized trial of denosumab in patients  receiving adjuvant aromatase inhibitors for nonmetastatic breast cancer.  Journal of Clinical Oncology. 2008;26:4875-4882.
 
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