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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前列腺癌转移阉割前列腺癌的成本效益分析

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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. 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. 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. 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:我们的研究目的是评估卡扎特·克拉特隆的成本效益,对患者的转移性阉割的前列腺癌(MCRPC)在预先用12?月内进行进展的多西紫杉醇治疗的转移性阉割的前列腺癌(MCRPC),同时接受替代抑制剂(AbiraTerone或eNzalutamide )来自美国付款人的观点。为了进行成本效益分析,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),并将增量成本效益率(ICER)视为主要终点。愿意支付(WTP)门槛设定为100,000.00美元/质量调整的终身年份(QALY),每年折扣率为3%。效力数据来自卡试验,并模拟了威布尔分布曲线以适应生存曲线。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。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和49,487.03美元,其推荐给了309,293.94美元/ QALY。我们的模型对Cabazitaxel集团的PFS持续时间大多敏感,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。与先前在接受astis的12个月内有进展的多西紫杉醇治疗的MCRPC患者的患者相比,Cabazitaxel不太可能是一种经济有效的治疗选择。

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