Cost-effectiveness of enzalutamide with androgen-deprivation therapy (ADT) versus ADT alone for the treatment of high-risk biochemically recurrent non-metastatic castration-sensitive prostate cancer in Canada.

IF 2.9 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Journal of Medical Economics Pub Date : 2025-12-01 Epub Date: 2025-05-23 DOI:10.1080/13696998.2025.2503660
Armen Aprikian, Fred Saad, Ewa Wywial, Thomas McLean, Karissa Johnston, Yuxin Li, Andrew Chilelli
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引用次数: 0

Abstract

Aim: The EMBARK (NCT02319837) trial demonstrated that enzalutamide with androgen-deprivation therapy (ADT; enzalutamide combination) or without ADT (enzalutamide monotherapy) significantly improved metastasis-free survival compared with ADT alone in high-risk biochemically recurrent (BCR) non-metastatic castration-sensitive prostate cancer (nmCSPC; also known as non-metastatic hormone-sensitive prostate cancer [nmHSPC]). No new safety signals were observed during the trial. The findings of EMBARK led to Health Canada's approval of enzalutamide for this patient population. The aim of this analysis was to assess the cost-effectiveness of enzalutamide combination versus ADT alone in patients with high-risk BCR nmCSPC from the Canadian payer's perspective.

Material and methods: A semi-Markov model was created to represent the treatment and disease progression of patients with high-risk BCR nmCSPC over a 30-year horizon. Costs and outcomes were discounted at 1.5% annually. Treatment effects for high-risk BCR nmCSPC were informed by data from the EMBARK trial. Life-years (LYs), quality-adjusted life-years (QALYs), lifetime costs and incremental cost-effectiveness ratio (ICER) were estimated for enzalutamide combination and ADT alone. A one-way sensitivity analysis (OWSA) and scenario analyses were conducted to assess the robustness of results.

Results: In the base-case deterministic analysis over the modeled time horizon, enzalutamide combination accumulated 11.85 LYs and 8.96 QALYs versus 8.75 LYs and 6.24 QALYs for ADT alone. The total cost for enzalutamide combination was Canadian dollars (CAD) 166,199, compared with CAD 95,146 for ADT alone. When combining cost and clinical outcome data, enzalutamide combination was associated with an ICER of CAD 26,129 per QALY gained. The OWSA and scenario analysis results were consistent with the base-case results.

Conclusion: The study findings suggest that enzalutamide combination was associated with an ICER of CAD 26,129 per QALY gained, which is within the standard Canadian thresholds for willingness-to-pay (i.e.

在加拿大,恩杂鲁胺联合雄激素剥夺疗法(ADT)与单独ADT治疗高风险生化复发性非转移性去势敏感前列腺癌的成本-效果比较。
目的:EMBARK (NCT02319837)试验表明,恩杂鲁胺与雄激素剥夺治疗(ADT;在高危生化复发(BCR)非转移性去势敏感前列腺癌(nmCSPC;也被称为非转移性激素敏感性前列腺癌[nmHSPC])。在试验期间没有观察到新的安全信号。EMBARK的研究结果促使加拿大卫生部批准对这类患者使用恩杂鲁胺。本分析的目的是从加拿大支付款人的角度评估enzalutamide联合与ADT单独治疗高风险BCR nmCSPC患者的成本效益。材料和方法:建立了一个半马尔可夫模型,以表示高风险BCR nmCSPC患者在30年内的治疗和疾病进展。成本和结果按每年1.5%折现。根据EMBARK试验的数据,可以得知高风险BCR nmCSPC的治疗效果。评估enzalutamide联合用药和ADT单独用药的生命年(LYs)、质量调整生命年(QALYs)、生命期成本和增量成本-效果比(ICER)。采用单向敏感性分析(OWSA)和情景分析来评估结果的稳健性。结果:在模型时间范围内的基本情况确定性分析中,enzalutamide联合用药累积了11.85个LYs和8.96个QALYs,而ADT单独用药累积了8.75个LYs和6.24个QALYs。enzalutamide联合治疗的总成本为166,199加元,而单独使用ADT的总成本为95146加元。当综合成本和临床结果数据时,enzalutamide联合使用与每获得QALY的ICER为26,129加元相关。OWSA和情景分析结果与基本情况结果一致。结论:研究结果表明,enzalutamide联合用药与每QALY获得的ICER为26,129加元相关,这在加拿大标准的支付意愿阈值(即:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Economics
Journal of Medical Economics HEALTH CARE SCIENCES & SERVICES-MEDICINE, GENERAL & INTERNAL
CiteScore
4.50
自引率
4.20%
发文量
122
期刊介绍: Journal of Medical Economics'' mission is to provide ethical, unbiased and rapid publication of quality content that is validated by rigorous peer review. The aim of Journal of Medical Economics is to serve the information needs of the pharmacoeconomics and healthcare research community, to help translate research advances into patient care and be a leader in transparency/disclosure by facilitating a collaborative and honest approach to publication. Journal of Medical Economics publishes high-quality economic assessments of novel therapeutic and device interventions for an international audience
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