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首页> 外文期刊>Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research >A trial-based assessment of the cost-utility of Bevacizumab and chemotherapy versus chemotherapy alone for advanced non-small cell lung cancer
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A trial-based assessment of the cost-utility of Bevacizumab and chemotherapy versus chemotherapy alone for advanced non-small cell lung cancer

机译:试行的评估成本效用的贝伐单抗和化疗和化疗在先进的非小细胞肺癌

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摘要

Objectives: Bevacizumab is approved for treatment of advanced non-small cell lung cancer (NSCLC) in combination with chemotherapy based on a 2-month median survival benefit demonstrated in one randomized trial. The cost-utility of adding bevacizumab to chemotherapy in advanced NSCLC remains unknown. We evaluated the cost-utility of bevacizumab added to chemotherapy in patients with advanced NSCLC. Methods: We developed a Markov model to estimate quality-adjusted life years (QALYs) and direct medical costs from the US payer perspective in patients treated with bevacizumab plus chemotherapy and compared these outcomes with patients treated with chemotherapy alone. We populated the model with survival and toxicity data from the clinical trial that compared the two strategies. We obtained utilities from a literature search and unit costs from Medicare. We discounted QALYs and costs at 3% per year. We addressed uncertainty with one-way and probabilistic sensitivity analyzes. Results: Compared with chemotherapy alone, bevacizumab and chemotherapy increased mean QALYs by 0.13, at an incremental life-time cost of US$72,000 per patient. The incremental cost-utility ratio (ICUR) was US$560,000/QALY. The ICUR was most sensitive to the survival on bevacizumab treatment, the drug costs of bevacizumab, and the utility of stable disease on treatment. At a threshold of US$100,000/QALY, the addition of bevacizumab had a 0.2% probability of being cost-effective. Conclusions: Bevacizumab does not appear to be cost-effective when added to chemotherapy in patients with advanced NSCLC, based on approximate cost-effectiveness thresholds that have been identified in the United States. These results may inform decision-makers about resource allocation for NSCLC care.
机译:目的:贝伐单抗是批准用于治疗先进的非小细胞肺癌(NSCLC)结合基于一个两个月的化疗中位数生存受益了随机试验。贝伐单抗在晚期非小细胞肺癌化疗仍然是未知的。贝伐单抗化疗的病人晚期非小细胞肺癌。马尔可夫模型来估计质量调整生命年(qaly)和直接的医疗费用我们在患者支付角度贝伐单抗+化疗和这些相比结果患者接受化疗一个人。毒性临床试验的数据比较了两种策略。从文献检索和单位成本的工具从医疗保险。每年3%。单向和概率敏感性分析。结果:与单独化疗相比,贝伐单抗和化疗增加意味着提升0.13,在增量成本一生72000美元每个病人。成本效用比率(ICUR) /提升560000美元。ICUR是最敏感的生存贝伐单抗治疗,药物的成本贝伐单抗和公用事业稳定的疾病治疗。贝伐单抗的概率0.2%是划算的。当添加似乎并不划算在晚期非小细胞肺癌患者化疗,基于近似成本效益已确定的阈值美国。决策者对资源分配非小细胞肺癌治疗。

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