Cancer treatment-induced bone loss: Pathophysiology and clinical perspectives

被引:58
作者
Brufsky, Adam M. [1 ]
机构
[1] Univ Pittsburgh, Magee Womens Hosp, Sch Med, Suite 4628, Pittsburgh, PA 15213 USA
关键词
androgen deprivation therapy; aromatase inhibitor; bisphosphonate; bone loss; osteoporosis; zoledronic acid;
D O I
10.1634/theoncologist.2007-0152
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Hormone-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.
引用
收藏
页码:187 / 195
页数:9
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