Impact of denosumab on bone mass in cancer patients

被引:7
|
作者
Brown-Glaberman, Ursa [1 ]
Stopeck, Alison T. [1 ]
机构
[1] Univ Arizona, Ctr Canc, 1515 N Campbell Ave, Tucson, AZ 85724 USA
关键词
denosumab; osteoporosis; osteopenia; hormone ablation therapy; cancer therapyinduced bone loss; chemotherapy;
D O I
10.2147/CPAA.S30330
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer therapy-induced bone loss (CTIBL) is a form of secondary osteoporosis associated with systemic chemotherapy and hormonal ablation therapy. The monitoring and treatment of CTIBL is an important component of comprehensive cancer care, especially for patients with curable disease and long life expectancies. Whereas oral bisphosphonates remain the most commonly used therapeutic option for CTIBL, additional treatment options may be required for patients who do not respond adequately or are intolerant to bisphosphonates, have renal insufficiency, or are receiving treatment with nephrotoxic medications. For these patients, denosumab, a monoclonal antibody targeting the receptor activator of nuclear factor-kappa B ligand (RANKL), offers an effective and well-tolerated alternative. Several recent randomized trials have examined the use of denosumab as treatment for CTIBL associated with hormone ablation therapy for breast and prostate cancer. Recent data suggest a possible role for RANKL inhibitors in both chemoprevention and the prevention of cancer recurrence through direct effects on breast tissue and breast cancer stem cells. The outcomes of several international Phase III clinical trials currently underway will help clarify the role of denosumab in patients undergoing cancer therapy.
引用
收藏
页码:117 / 129
页数:13
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