New Mexico Clinical Research & Osteoporosis Center, Albuquerque, NM.
Department of Medicine (Endocrinology), University of British Columbia, Vancouver, Canada.
Am J Med. 2019 Nov;132(11):e771-e777. doi: 10.1016/j.amjmed.2019.04.044. Epub 2019 May 29.
Patients often start treatment to reduce fracture risk because of a bone mineral density T-score consistent with osteoporosis (≤ -2.5). Others with a T-score above -2.5 may be treated when there is a history of fragility fracture or when a fracture risk algorithm categorizes them as having a high risk for fracture. It is common to initiate therapy with a generic oral bisphosphonate, unless contraindicated, and continue therapy if the patient is responding as assessed by stability or an increase in bone mineral density. However, some patients may respond well to an oral bisphosphonate, yet remain with an unacceptably high risk for fracture. Recognition of this occurrence has led to the development of an alternative strategy: treat-to-target. This involves identifying a biological marker (treatment target) that represents an acceptable fracture risk and then initiating treatment with an agent likely to reach this target. If the patient is on a path to reaching the target with initial therapy, treatment is continued. If it appears the target will not be reached with initial therapy, treatment is changed to an agent more likely to achieve the goal.
患者通常会因骨密度 T 评分符合骨质疏松症(≤-2.5)而开始治疗以降低骨折风险。其他 T 评分高于-2.5 的患者,如果有脆性骨折史或骨折风险算法将其归类为骨折高风险,则可能会接受治疗。通常会首先使用一种通用的口服双膦酸盐进行治疗,除非有禁忌症,如果患者通过稳定性或骨密度增加来评估有反应,则继续治疗。但是,有些患者可能对口服双膦酸盐反应良好,但骨折风险仍然很高。认识到这种情况的发生,导致了一种替代策略的发展:针对目标治疗。这涉及确定一个代表可接受骨折风险的生物标志物(治疗目标),然后用可能达到该目标的药物开始治疗。如果患者在初始治疗中朝着达到目标的方向前进,则继续治疗。如果初始治疗似乎无法达到目标,则将治疗方案更改为更有可能实现目标的药物。