University of Cincinnati Bone Health and Osteoporosis Center, Cincinnati VA Medical Center, Division of Endocrinology/Metabolism, Department of Internal Medicine , 260 Stetson St, Suite 4200, Cincinnati, OH 45219 , USA +1 513 558 4444 ; +1 513 558 8581 ;
Expert Opin Drug Saf. 2014 Feb;13(2):247-53. doi: 10.1517/14740338.2014.860133. Epub 2013 Dec 2.
Denosumab is a fully human monoclonal antibody against the receptor activator of nuclear factor kappa-B ligand. It is an antiresorptive agent that reduces osteoclastogenesis.
This drug evaluation reviews denosumab for use in osteoporosis. Denosumab has been shown to improve bone mineral density (BMD) and to reduce the incidence of new vertebral, hip and nonvertebral fractures in postmenopausal women. It prevents bone loss and reduces vertebral fracture risk in men with nonmetastatic prostate cancer who are receiving androgen deprivation therapy. It has also been shown to improve BMD in men with osteoporosis unrelated to androgen deprivation therapy. Safety concerns include infections, cancer, skin reactions, cardiovascular disease, hypocalcemia, osteonecrosis of the jaw and atypical femur fractures.
Although bisphosphonates are typically preferred as initial therapy for osteoporosis, denosumab could be used as initial therapy in select patients at high risk for fracture, including older patients who have difficulty with the dosing requirements of oral bisphosphonates, patients who are intolerant of or unresponsive to other therapies, and in those with impaired renal function. Additional data is needed to address issues regarding treatment duration and discontinuation, as well as to provide more information regarding denosumab's efficacy and safety.
地舒单抗是一种针对核因子-κB 配体受体激活剂的全人源单克隆抗体。它是一种抗吸收剂,可减少破骨细胞形成。
本药物评估回顾了地舒单抗在骨质疏松症中的应用。地舒单抗已被证明可改善骨密度(BMD)并降低绝经后妇女新发椎体、髋部和非椎体骨折的发生率。它可预防接受雄激素剥夺治疗的非转移性前列腺癌男性的骨质流失并降低椎体骨折风险。它还被证明可改善与雄激素剥夺治疗无关的骨质疏松症男性的 BMD。安全性问题包括感染、癌症、皮肤反应、心血管疾病、低钙血症、颌骨坏死和非典型股骨骨折。
虽然双膦酸盐通常是骨质疏松症初始治疗的首选药物,但对于骨折风险高的特定患者,包括难以满足口服双膦酸盐剂量要求的老年患者、对其他治疗不耐受或无反应的患者以及肾功能受损的患者,地舒单抗可作为初始治疗药物。需要更多的数据来解决关于治疗持续时间和停药的问题,并提供更多关于地舒单抗疗效和安全性的信息。