Morgans Alicia K, Smith Matthew R
Division of Hematology/Oncology, Massachusetts General Hospital Cancer Center, POB 221, Boston, MA 02114, USA.
J Osteoporos. 2011;2011:941310. doi: 10.4061/2011/941310. Epub 2011 Oct 15.
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.
男性骨质疏松症是老年男性中一个日益受到关注的问题。男性骨质疏松症的一个常见病因是性腺功能减退。数以千计的前列腺癌患者接受雄激素剥夺治疗,这种治疗会显著降低血清睾酮水平并导致严重的性腺功能减退。接受雄激素剥夺治疗的男性骨矿物质密度下降,骨折发生率增加。本文将前列腺癌幸存者作为性腺功能减退性骨质疏松症的一个模型进行描述,并讨论了RANKL靶向治疗在骨质疏松症中的应用。地诺单抗是目前唯一可用的RANKL靶向治疗药物,它可增加前列腺癌男性患者的骨矿物质密度并降低骨折发生率。地诺单抗还与首次骨相关事件发生时间的延迟以及这些男性患者无骨转移生存期的延长有关。研究RANKL靶向治疗在普通人群男性骨质疏松症中的应用是合理的。