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度他雄胺治疗晚期激素依赖性前列腺癌的成本效果分析。

Cost-effectiveness analysis of degarelix for advanced hormone-dependent prostate cancer.

机构信息

PenTAG, Peninsula College of Medicine and Dentistry, University of Exeter, UK.

出版信息

BJU Int. 2012 Apr;109(8):1183-92. doi: 10.1111/j.1464-410X.2011.10434.x. Epub 2011 Aug 23.

Abstract

OBJECTIVE

To evaluate the cost-effectiveness of degarelix vs luteinizing hormone-releasing hormone analogue (triptorelin) plus short-term antiandrogen treatment for advanced prostate cancer.

METHODS

We developed a decision analytic model based on a clinical trial and literature review. The two interventions evaluated were: (i) monthly injection of degarelix and (ii) 3-monthly triptorelin therapy plus short-term flutamide, cyproterone or bicalutamide treatment. The model consisted of a decision tree monitoring a hypothetical cohort of patients aged 70 years from the start of hormonal treatment to the end of the first month, and a Markov model monitoring patients from the end of month 1 for a time horizon of 10 years (i.e. when 96% of patients are assumed to have died). The base-case analysis assumed patients present with asymptomatic metastatic prostate cancer. Costs and outcomes were collected over the model time horizon. Outcome measures were quality-adjusted life years (QALYs), lifetime costs and incremental cost-effectiveness ratios. Sensitivity analyses (one-way and multi-way) and probabilistic sensitivity analyses were conducted to explore the uncertainties around the assumptions.

RESULTS

In the base-case analysis, the incremental cost-effectiveness ratio (ICER) for degarelix vs triptorelin plus antiandrogen was £59,000 per QALY gained. The model was most sensitive to the rate of significant adverse events in the triptorelin plus antiandrogen group. The model was also sensitive to the assumed survival of patients with metastatic prostate cancer and the price of degarelix. The results of the probabilistic sensitivity analyses suggested that there was a low probability (9.6%) of degarelix being the most cost-effective treatment option when a willingness-to-pay threshold of £30,000 per QALY gained is assumed.

CONCLUSION

Degarelix is unlikely to be cost-effective compared to triptorelin plus short-term antiandrogen in the management of advanced prostate cancer with respect to the usual thresholds of cost-effectiveness used in the UK: £20,000-30,000 per QALY gained (used by the National Institute for Health and Clinical Excellence).

摘要

目的

评估去势受体抑制剂(地加瑞克)与促黄体生成素释放激素类似物(亮丙瑞林)联合短期抗雄激素治疗晚期前列腺癌的成本效益。

方法

我们基于临床试验和文献回顾开发了一个决策分析模型。评估的两种干预措施是:(i)每月注射地加瑞克;(ii)每 3 个月注射亮丙瑞林联合短期氟他胺、环丙孕酮或比卡鲁胺治疗。该模型由一个决策树组成,该决策树从开始激素治疗到第一个月结束监测一个假设的 70 岁患者队列;一个马尔可夫模型从第一个月末开始监测患者,时间范围为 10 年(即假设 96%的患者已死亡)。基本案例分析假设患者患有无症状转移性前列腺癌。在模型时间范围内收集成本和结果。结果测量是质量调整生命年(QALY)、终生成本和增量成本效益比。进行了敏感性分析(单向和多向)和概率敏感性分析,以探索假设的不确定性。

结果

在基本案例分析中,地加瑞克与亮丙瑞林联合抗雄激素治疗的增量成本效益比(ICER)为每获得一个 QALY 增加 59,000 英镑。该模型对亮丙瑞林联合抗雄激素组中严重不良事件的发生率最为敏感。该模型还对转移性前列腺癌患者的预期生存和地加瑞克的价格敏感。概率敏感性分析的结果表明,当假设获得每 QALY 增加 30,000 英镑的意愿支付阈值时,地加瑞克成为最具成本效益的治疗方案的可能性很低(9.6%)。

结论

就英国常用的成本效益阈值(每获得一个 QALY 增加 20,000-30,000 英镑)而言,与亮丙瑞林联合短期抗雄激素治疗相比,地加瑞克不太可能在晚期前列腺癌的管理中具有成本效益(国家卫生与临床优化研究所使用)。

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