Curr Oncol. 2008 Jan;15(Suppl 1):S30-40. doi: 10.3747/co.2008.174.
Cancer therapy can result in significant bone loss and increased risk of fragility fracture. Chemotherapy, aromatase inhibitors, and gonadotropin-releasing hormone analogues contribute to increases in the rate of bone remodelling and reduce bone mineral density. Patients with prostate cancer on androgen deprivation therapy experience an increase in the risk of fracture. New research has demonstrated the key role played by bisphosphonates in preventing declines in bone density and increases in bone remodelling. Novel antiresorptive agents targeting receptor activator of nuclear factor κB ligand have great potential in skeletal protection and prevention of bone loss related to cancer therapy. Early assessment of skeletal health, followed by initiation of calcium, vitamin D, and an exercise program are valuable in the prevention and treatment of osteoporosis. In addition, individuals at increased risk for fracture should be offered antiresorptive therapy. Early data have demonstrated that bisphosphonates are able to prevent the bone loss and increased bone remodelling associated with cancer therapy, including aromatase inhibition and androgen deprivation therapy. The present paper reviews the new research and advances in the management of bone loss associated with both cancer therapy and estrogen deficiency in the postmenopausal female.
癌症治疗会导致明显的骨质流失和脆性骨折风险增加。化疗、芳香化酶抑制剂和促性腺激素释放激素类似物会增加骨重塑的速度并降低骨密度。接受雄激素剥夺治疗的前列腺癌患者骨折风险增加。新的研究表明,双膦酸盐在预防骨密度下降和骨重塑增加方面发挥着关键作用。针对核因子κB 配体受体激活剂的新型抗吸收剂在骨骼保护和预防与癌症治疗相关的骨质流失方面具有巨大潜力。早期评估骨骼健康状况,然后开始补钙、维生素 D 和进行锻炼,对于预防和治疗骨质疏松症非常有价值。此外,应向骨折风险增加的个体提供抗吸收治疗。早期数据表明,双膦酸盐能够预防与癌症治疗相关的骨质流失和骨重塑增加,包括芳香化酶抑制和雄激素剥夺治疗。本文综述了与癌症治疗和绝经后女性雌激素缺乏相关的骨质流失管理方面的新研究和进展。