Probability of achieving bone mineral density treatment goals with denosumab treatment in postmenopausal women with osteoporosis.

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Felicia Cosman, Zhenxun Wang, Xiaodong Li, Steven R Cummings
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Abstract

BMD levels achieved on osteoporosis treatment are predictive of subsequent fracture risk, and T-score >-2.5 has been proposed as a minimum treatment target for women with osteoporosis. Knowing the likelihood of attaining target T-scores with different medications for different baseline BMD levels can help determine appropriate initial treatment for individual patients. In this post hoc analysis, we estimated the probability of achieving a non-osteoporotic T-score (>-2.5 or ≥-2.0) at the TH or LS in postmenopausal women >60 yr old treated with denosumab for either 3 or 10 yr in the FREEDOM trial and its long-term extension. In women with baseline TH T-scores of -2.7, -3.0, and -3.5, the probabilities of achieving target T-scores >-2.5 with 3 yr of denosumab were 71%, 12%, and 0.1%, respectively. At LS, for baseline T-scores of -2.7, -3.0, and -3.5, the probabilities were 86%, 59%, and 11%, respectively. Longer treatment duration of up to 10 yr increased the probability of achieving target T-scores. The baseline T-scores that permitted at least 50% of women to achieve a target T-score >-2.5 were -2.8 at TH and -3.1 at LS after 3 yr and -3.0 at TH and -3.7 at LS after 10 yr of treatment. To achieve higher treatment targets (T-scores ≥ -2.0), overall probabilities were lower at both skeletal sites, particularly for TH, even with longer treatment duration. Our results demonstrate that the probability of achieving T-score targets with denosumab is dependent on baseline BMD, skeletal site, and treatment duration. Knowing the probability of achieving treatment targets for different baseline TH and LS T-scores can help determine whether denosumab is an appropriate first choice of treatment in individual patients.

Denosumab治疗绝经后骨质疏松症妇女达到骨密度治疗目标的可能性。
骨质疏松症治疗中达到的骨密度(BMD)水平可预测随后的骨折风险,已提出将t评分> -2.5作为骨质疏松症女性的最低治疗目标。了解不同基线骨密度水平的不同药物达到目标t评分的可能性可以帮助确定适合个体患者的初始治疗。在这项事后分析中,我们估计了在FREEDOM试验及其长期延长中,接受denosumab治疗3年或10年的绝经后妇女>60岁在全髋(TH)或腰椎(LS)达到非骨质疏松性t评分(> -2.5或≥-2.0)的概率。基线TH t评分为-2.7,-3.0和-3.5的女性,在denosumab治疗3年后达到目标t评分bb0 -2.5的概率分别为71%,12%和0.1%。在LS,基线t得分为-2.7,-3.0和-3.5时,概率分别为86%,59%和11%。治疗时间延长至10年增加了达到目标t评分的可能性。基线t评分允许至少50%的女性达到目标t评分> -2.5,治疗3年后,TH组为-2.8,LS组为-3.1,治疗10年后,TH组为-3.0,LS组为-3.7。为了达到更高的治疗目标(t评分≥-2.0),即使治疗时间较长,两个骨骼部位的总体概率也较低,尤其是TH。我们的研究结果表明,denosumab达到t评分目标的概率取决于基线BMD、骨骼部位和治疗时间。了解不同基线TH和LS t评分达到治疗目标的概率可以帮助确定denosumab是否适合个体患者的首选治疗。
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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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