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骨转移乳腺癌和去势抵抗性前列腺癌患者中 12 周与 4 周给药骨靶向药物的成本效果分析。

Cost-Effectiveness Analysis of 12-Versus 4-Weekly Administration of Bone-Targeted Agents in Patients with Bone Metastases from Breast and Castration-Resistant Prostate Cancer.

机构信息

Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON K1H 8L6, Canada.

Faculty of Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.

出版信息

Curr Oncol. 2021 May 13;28(3):1847-1856. doi: 10.3390/curroncol28030171.

Abstract

A cost-utility analysis was performed based on the Rethinking Clinical Trials (REaCT) bone-targeted agents (BTA) clinical trial that compared 12-weekly (once every 12 weeks) ( = 130) versus 4-weekly (once every 4 weeks) ( = 133) BTA dosing for metastatic breast and castration-resistant prostate (CRPC) cancer. Using a decision tree model, we calculated treatment and symptomatic skeletal event (SSE) costs as well as quality-adjusted life-years (QALYs) for each treatment option. Deterministic and probabilistic sensitivity analyses were performed to assess the robustness of the study findings. The total cost of BTA treatment in Canadian dollars (C$) and estimated QALYs was C$8965.03 and 0.605 QALY in the 4-weekly group versus C$5669.95 and 0.612 QALY in the 12-weekly group, respectively. De-escalation from 4-weekly to 12-weekly BTA reduces cost (C$3293.75) and improves QALYs by 0.008 unit, suggesting that 12-weekly BTA dominates 4-weekly BTA in breast and CRPC patients with bone metastases. Sensitivity analysis suggests high levels of uncertainty in the cost-effectiveness findings. De-escalation of bone-targeted agents is cost-effective from the Canadian public payer's perspective.

摘要

基于比较转移性乳腺癌和去势抵抗性前列腺癌(CRPC)患者每 12 周(=130 例)与每 4 周(=133 例)接受骨靶向药物(BTA)治疗的疗效和安全性的重新思考临床试验(REaCT)BTA 临床试验,进行了成本效用分析。使用决策树模型,我们计算了每种治疗方案的治疗和症状性骨骼事件(SSE)成本以及质量调整生命年(QALY)。进行了确定性和概率敏感性分析,以评估研究结果的稳健性。在加拿大元(C$)中,4 周组的 BTA 治疗总成本和估计的 QALY 分别为 C$8965.03 和 0.605 QALY,而 12 周组分别为 C$5669.95 和 0.612 QALY。从每 4 周 BTA 降阶至每 12 周 BTA 可降低成本(C$3293.75)并使 QALY 增加 0.008 个单位,表明在有骨转移的乳腺癌和 CRPC 患者中,每 12 周 BTA 优于每 4 周 BTA。敏感性分析表明,成本效益结果存在高度不确定性。从加拿大公共支付者的角度来看,降低骨靶向药物的剂量具有成本效益。

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