Gilbert Scott M, McKiernan James M
Department of Urology, University of Michigan, Ann Arbor, MI 49109, USA.
Urol Clin North Am. 2006 May;33(2):191-9, vi. doi: 10.1016/j.ucl.2005.12.009.
Androgen deprivation therapy (ADT) is associated with a significant decrease in bone mineral density (BMD), and continued exposure seems to increase the risk of osteoporotic fracture in men who have prostate cancer treated with this strategy. Men who have prostate cancer may have low BMD before initiation of ADT. Bisphosphonates are pyrophosphate analogs that decrease bone resorption primarily through direct inhibition of osteoclast activity and proliferation. Several bisphosphonates have been evaluated in randomized clinical trials, and the cumulative data show that these medications increase or maintain BMD in men receiving ADT for prostate cancer. The effect on clinical fractures has not been assessed adequately, but bisphosphonates offer an important potential treatment modality to reduce the risk of osteoporotic fracture in this population of men.
雄激素剥夺疗法(ADT)与骨矿物质密度(BMD)显著降低相关,持续暴露似乎会增加采用该策略治疗的前列腺癌男性发生骨质疏松性骨折的风险。患有前列腺癌的男性在开始ADT之前可能就存在低骨密度。双膦酸盐是焦磷酸盐类似物,主要通过直接抑制破骨细胞活性和增殖来减少骨吸收。多项双膦酸盐已在随机临床试验中进行评估,累积数据表明,这些药物可使接受ADT治疗前列腺癌的男性骨密度增加或维持在原有水平。对临床骨折的影响尚未得到充分评估,但双膦酸盐为降低该男性群体骨质疏松性骨折风险提供了一种重要的潜在治疗方式。