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Cost-effectiveness analysis of cabazitaxel for metastatic castration resistant prostate cancer after docetaxel and androgen-signaling-targeted inhibitor resistance

机译:Cabazitaxel在多西紫杉醇和雄激素信号抑制剂抗性后转移阉割前列腺癌的Cabazitaxel成本效果分析

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摘要

Abstract Background The aim of our study was to evaluate the cost-effectiveness of cabazitaxel versus abiraterone or enzalutamide in patients with metastatic castration-resistant prostate cancer (mCRPC) previously treated with docetaxel who had progression within 12 months while receiving an alternative inhibitor (abiraterone or enzalutamide) from a US payer’s perspective. Methods To conduct the cost-effectiveness analysis, a Markov decision model was established. Three health states (progression-free survival (PFS), progressive disease (PD) and death) were included, and the incremental cost-effectiveness ratio (ICER) was regarded as the primary endpoint. The willingness-to-pay (WTP) threshold was set at $100,000.00/quality-adjusted life year (QALY), and discounted rates were set at 3% annually. Efficacy data were derived from the CARD trial and Weibull distribution curves were modeled to fit the survival curves. The robustness of the analysis was tested with a series of one-way sensitivity analyses and probabilistic sensitivity analyses. Results Overall, the incremental effectiveness and cost of cabazitaxel versus androgen-signaling-targeted inhibitors (ASTIs) were 0.16 QALYs and $49,487.03, respectively, which yielded an ICER of $309,293.94/QALY. Our model was mostly sensitive to the duration of PFS in the cabazitaxel group, cost of cabazitaxel and utility of the PFS state. At a WTP threshold of $100,000.00/QALY, cabazitaxel was the dominant strategy in 0% of the simulations. Conclusions Cabazitaxel is unlikely to be a cost-effective treatment option compared with ASTIs in patients with mCRPC previously treated with docetaxel who had progression within 12 months while receiving ASTIs.
机译:摘要背景技术我们的研究目的是评估卡泽特克西克氏素对Abiraaterone或苯甲胺酮的成本效益,所述转移性阉割的前列腺癌(MCRPC)在接受替代抑制剂(AbiraTerone或来自美国付款人的角度来看依纳腊肠酰胺。进行成本效益分析的方法,建立了马尔可夫决策模型。包括三种健康状况(无进展生存(PFS),渐进性疾病(PD)和死亡),递增成本效益率(ICER)被视为主要终点。愿意付费(WTP)门槛设定为100,000.00美元/质量调整的终身年(QALY),每年折扣率为3%。功效数据来自卡试验,并模拟了威布尔分布曲线以适应存活曲线。通过一系列单向敏感性分析和概率敏感性分析测试了分析的稳健性。结果总体而言,Cabazitaxel与雄激素信号靶向抑制剂(Astis)的增量效力和成本分别为0.16 qalys,分别为49,487.03美元,占用了309,293.94美元/ QALY。我们的模型对CabaziteL组的PFS持续时间大致敏感,CabaziteL的成本和PFS状态的效用。在100,000.00美元/ Qaly的WTP阈值下,Cabazitaxel是0%的仿真战略。结论卡泽特克斯不太可能是一种经济效益的治疗选择,与MCRPC先前用多西紫杉醇治疗的MCRPC患者的哮喘相比,在接受astis的同时在12个月内进行进展。

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