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美国绝经后骨质疏松症女性中,10年地诺单抗与阿仑膦酸钠成本效益的全面更新。

A comprehensive update on the cost-effectiveness of 10-year denosumab vs alendronate in postmenopausal women with osteoporosis in the United States.

作者信息

Yeh Eric, Saeedian Matia, Badaracco Jack

机构信息

Amgen Inc, Thousand Oaks, CA, USA.

BluePath Solutions, Los Angeles, CA, USA.

出版信息

Arch Osteoporos. 2025 Jun 30;20(1):85. doi: 10.1007/s11657-025-01564-x.

Abstract

UNLABELLED

In postmenopausal women with osteoporosis, 10-year denosumab was estimated to be cost-effective vs 5 years of oral alendronate, a 2-year drug holiday, and subsequently 3-years of alendronate with an estimated incremental cost-effectiveness ratio of $97,574 per quality-adjusted life-years gained. Cost-effectiveness was demonstrated in most of the scenario simulations.

PURPOSE

A previous economic analysis estimated that 5-year denosumab was cost-effective compared with 5-year alendronate in women with postmenopausal osteoporosis (PMO) in the United States (US). Emerging literature has provided data on the long-term clinical benefits of denosumab. Therefore, the cost-effectiveness analysis was updated to understand the potential implications of a longer treatment duration (10-year) with denosumab vs generic oral alendronate or no treatment from a US third-party payer perspective.

METHODS

A lifetime Markov cohort model was used to compare 10-year denosumab treatment to 5 years of alendronate, followed by a 2-year drug holiday and, then an additional 3 years of alendronate. The target population consisted of PMO women in the US with a starting age of 72 years. Recent publicly available data, including epidemiology, treatment efficacy, persistence, and costs, were used to inform model inputs. Scenario analyses and a probabilistic sensitivity analysis (PSA) were conducted to account for uncertainty.

RESULTS

Estimated mean total lifetime cost and quality-adjusted life years (QALYs), respectively, were $81,003 and 8.035 for denosumab, and $75,358 and 7.977 for alendronate, resulting in denosumab having an incremental cost-effectiveness ratio of $97,574 per QALY gained. At a threshold of $150,000 per QALY, the PSA demonstrated that denosumab was considered cost effective in 62.1% of simulations. Denosumab was dominant over no treatment.

CONCLUSIONS

Ten-year denosumab treatment would be cost-effective compared with 5 years of alendronate, followed by a 2-year drug holiday and 3 years of alendronate at the threshold of $150,000. Cost-effectiveness was demonstrated across most scenarios with robust PSA results.

摘要

未标注

在患有骨质疏松症的绝经后女性中,估计10年的地诺单抗治疗与5年的口服阿仑膦酸钠、2年的药物假期,随后再进行3年的阿仑膦酸钠治疗相比具有成本效益,每获得一个质量调整生命年的增量成本效益比估计为97,574美元。在大多数情景模拟中都证明了成本效益。

目的

先前的一项经济分析估计,在美国,5年的地诺单抗治疗与5年的阿仑膦酸钠治疗相比,对于绝经后骨质疏松症(PMO)女性具有成本效益。新出现的文献提供了关于地诺单抗长期临床益处的数据。因此,从美国第三方支付方的角度,更新成本效益分析以了解使用地诺单抗进行更长疗程(10年)治疗与使用普通口服阿仑膦酸钠或不治疗相比的潜在影响。

方法

使用终身马尔可夫队列模型将10年的地诺单抗治疗与5年的阿仑膦酸钠治疗进行比较,随后是2年的药物假期,然后再进行3年的阿仑膦酸钠治疗。目标人群为美国72岁开始的PMO女性。使用包括流行病学、治疗效果、持续性和成本等近期公开可用的数据来为模型输入提供信息。进行情景分析和概率敏感性分析(PSA)以考虑不确定性。

结果

地诺单抗的估计平均终身总成本和质量调整生命年(QALY)分别为81,003美元和8.035,阿仑膦酸钠分别为75,358美元和7.977,导致地诺单抗每获得一个QALY的增量成本效益比为97,574美元。在每QALY 150,000美元的阈值下,PSA表明地诺单抗在62.1%的模拟中被认为具有成本效益。地诺单抗相对于不治疗具有优势。

结论

在每QALY 150,000美元的阈值下,10年的地诺单抗治疗与5年的阿仑膦酸钠治疗,随后是2年的药物假期和3年的阿仑膦酸钠治疗相比具有成本效益。在大多数情景中都证明了成本效益,PSA结果稳健。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cdc/12209382/8ee3400c4efb/11657_2025_1564_Fig1_HTML.jpg

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