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尼妥珠单抗治疗转移性鳞状非小细胞肺癌:建立基于价值的成本核算。

Necitumumab in Metastatic Squamous Cell Lung Cancer: Establishing a Value-Based Cost.

机构信息

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia.

H. Milton Stewart School of Industrial & Systems Engineering, Georgia Institute of Technology, Atlanta, Georgia.

出版信息

JAMA Oncol. 2015 Dec;1(9):1293-300. doi: 10.1001/jamaoncol.2015.3316.

Abstract

IMPORTANCE

The SQUIRE trial demonstrated that adding necitumumab to chemotherapy for patients with metastatic squamous cell lung cancer (mSqCLC) increased median overall survival by 1.6 months (hazard ratio, 0.84). However, the costs and value associated with this intervention remains unclear. Value-based pricing links the price of a drug to the benefit that it provides and is a novel method to establish prices for new treatments.

OBJECTIVE

To evaluate the range of drug costs for which adding necitumumab to chemotherapy could be considered cost-effective.

DESIGN, SETTING, AND PARTICIPANTS: We developed a Markov model using data from multiple sources, including the SQUIRE trial, which compared standard chemotherapy with and without necitumumab as first-line treatment of mSqCLC, to evaluate the costs and patient life expectancies associated with each regimen. In the analysis, patients were modeled to receive gemcitabine and cisplatin for 6 cycles or gemcitabine, cisplatin, and necitumumab for 6 cycles followed by maintenance necitumumab. Our model's clinical inputs were the survival estimates and frequency of adverse events (AEs) described in the SQUIRE trial. Log-logistic models were fitted to the survival distributions in the SQUIRE trial. The cost inputs included drug costs, based on the Medicare average sale prices, and costs for drug administration and management of AEs, based on Medicare reimbursement rates (all in 2014 US dollars).

MAIN OUTCOMES AND MEASURES

We evaluated incremental cost-effectiveness ratios (ICERs) for the use of necitumumab across a range of values for its cost. Model robustness was assessed by probabilistic sensitivity analyses, based on 10 000 Monte Carlo simulations, sampling values from the distributions of all model parameters.

RESULTS

In the base case analysis, the addition of necitumumab to the treatment regimen produced an incremental survival benefit of 0.15 life-years and 0.11 quality-adjusted life-years (QALYs). The probabilistic sensitivity analyses established that when necitumumab cost less than $563 and less than $1309 per cycle, there was 90% confidence that the ICER for adding necitumumab would be less than $100 000 per QALY and less than $200 000 per QALY, respectively.

CONCLUSIONS AND RELEVANCE

These findings provide a value-based range for the cost of necitumumab from $563 to $1309 per cycle. This study provides a framework for establishing value-based pricing for new oncology drugs entering the US marketplace.

摘要

重要性

SQUIRE 试验表明,在转移性鳞状非小细胞肺癌(mSqCLC)患者中,将 necitumumab 加入化疗可使中位总生存期延长 1.6 个月(风险比,0.84)。然而,这种干预措施的成本和价值仍不清楚。基于价值的定价将药物的价格与其提供的益处联系起来,是为新治疗方法确定价格的一种新方法。

目的

评估将 necitumumab 加入化疗的药物成本范围,以确定其具有成本效益。

设计、设置和参与者:我们使用来自多个来源的数据(包括 SQUIRE 试验)开发了一个马尔可夫模型,该模型比较了标准化疗与作为 mSqCLC 一线治疗的 necitumumab 联合化疗,以评估每个方案相关的成本和患者预期寿命。在分析中,模型假设患者接受吉西他滨和顺铂 6 个周期或吉西他滨、顺铂和 necitumumab 6 个周期后维持 necitumumab 治疗。我们模型的临床输入是 SQUIRE 试验中描述的生存估计和不良事件(AE)的频率。对数逻辑模型拟合了 SQUIRE 试验中的生存分布。成本输入包括基于医疗保险平均销售价格的药物成本,以及基于医疗保险报销率的药物管理和 AE 管理成本(均以 2014 年美元计)。

主要结果和措施

我们评估了 necitumumab 成本在一定范围内的增量成本效益比(ICER)。通过基于 10000 次蒙特卡罗模拟的概率敏感性分析评估模型稳健性,从所有模型参数的分布中抽样值。

结果

在基准分析中,在治疗方案中添加 necitumumab 可使生存获益增加 0.15 个生命年和 0.11 个质量调整生命年(QALY)。概率敏感性分析确定,当 necitumumab 的成本低于每周期 563 美元和 1309 美元时,有 90%的置信度认为添加 necitumumab 的 ICER 将低于每 QALY 100000 美元和每 QALY 200000 美元。

结论和相关性

这些发现为 necitumumab 的成本提供了一个基于价值的范围,即每周期 563 美元至 1309 美元。本研究为进入美国市场的新型肿瘤药物建立基于价值的定价提供了框架。

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