RANKL-Targeted Therapies: The Next Frontier in the Treatment of Male Osteoporosis
Author(s) -
Alicia K. Morgans,
Matthew R. Smith
Publication year - 2011
Publication title -
journal of osteoporosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.421
H-Index - 19
eISSN - 2090-8059
pISSN - 2042-0064
DOI - 10.4061/2011/941310
Subject(s) - medicine , denosumab , prostate cancer , osteoporosis , androgen deprivation therapy , rankl , bone mineral , oncology , bone metastasis , testosterone (patch) , population , endocrinology , cancer , receptor , environmental health , activator (genetics)
Male osteoporosis is an increasingly recognized problem in aging men. A common cause of male osteoporosis is hypogonadism. Thousands of men with prostate cancer are treated with androgen deprivation therapy, a treatment that dramatically reduces serum testosterone and causes severe hypogonadism. Men treated with androgen deprivation therapy experience a decline in bone mineral density and have an increased rate of fracture. This paper describes prostate cancer survivors as a model of hypogonadal osteoporosis and discusses the use of RANKL-targeted therapies in osteoporosis. Denosumab, the only RANKL-targeted therapy currently available, increases bone mineral density and decreases fracture rate in men with prostate cancer. Denosumab is also associated with delayed time to first skeletal-related event and an increase in bone metastasis-free survival in these men. It is reasonable to investigate the use of RANKL-targeted therapy in male osteoporosis in the general population.
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