Denosumab for the treatment of osteoporosis

被引:115
作者
Zaheer, Sarah [1 ]
LeBoff, Meryl [1 ]
Lewiecki, Michael [2 ]
机构
[1] Brigham & Womens Hosp, Boston, MA 02115 USA
[2] New Mexico Clin Res & Osteoporosis Ctr, Albuquerque, NM 87106 USA
关键词
denosumab; mAb; osteoporosis; receptor activator of nuclear factor kappa-B ligand; treatment; BONE-MINERAL DENSITY; POSTMENOPAUSAL WOMEN; VERTEBRAL FRACTURE; RANDOMIZED-TRIAL; ZOLEDRONIC ACID; HIP FRACTURE; RISK; ALENDRONATE; THERAPY; TERIPARATIDE;
D O I
10.1517/17425255.2015.1000860
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Introduction: Low trauma fractures due to osteoporosis are a major health concern worldwide. Despite the availability of many therapeutic compounds to reduce fracture risk, osteoporosis remains undertreated and the burden of osteoporotic fractures remains high. Denosumab is a novel agent that acts to reduce bone turnover, improve bone mineral density, and reduce fracture risk, offering a favorable efficacy and safety profile. Areas covered: This review covers the pharmacology and major clinical trials with extension/post-marketing follow-up, including trials for all FDA-approved indications of denosumab to date. Expert opinion: Denosumab is an efficacious and safe osteoporosis treatment option, with current data from up to 8 years of continued use showing continued improvement in bone density with sustained fracture risk reduction. Safety profiles overall are similar to placebo, with no new safety concerns in extension trials, though a theoretical increased risk of infection exists with RANKL inhibition. Future considerations include safety of prolonged treatment beyond 8 years, and efficacy/fracture risk after discontinuation or with non-adherence, given the characteristic pharmacodynamic profile of denosumab.
引用
收藏
页码:461 / 470
页数:10
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