Agency for Care Effectiveness,Ministry of Health,Singapore.
Division of Medical Oncology Singapore,Singapore.
Int J Technol Assess Health Care. 2019 Jan;35(2):126-133. doi: 10.1017/S0266462319000059. Epub 2019 Mar 11.
This study was conducted to evaluate the cost-effectiveness of sunitinib versus interferon-alfa for the treatment of advanced and/or metastatic renal cell carcinoma (RCC) in Singapore.
A partitioned survival model with three health states (progression-free, progressive disease, and death) was developed from a healthcare payer perspective over a 10-year time horizon. Survival curves from the pivotal trial of sunitinib versus interferon-alfa were extrapolated beyond the trial period to estimate the underlying progression-free survival and overall survival parametric distributions. Health state utilities were derived from the literature and direct costs were sourced from local public healthcare institutions. The sunitinib dose in the model reflected local prescribing practices whereby a combination of 50 mg (28 percent) and 37.5 mg (72 percent) strengths are used.
The base-case analysis comparing sunitinib versus interferon-alfa resulted in an incremental cost effectiveness ratio (ICER) of SGD191,061 (USD139,757) per quality-adjusted life-year gained. Sensitivity analysis demonstrated that the ICER was most sensitive to variations in the utility value assumed for the progression-free health state and the price of sunitinib.
In the absence of any price reduction, sunitinib had an exceedingly high ICER and was not considered a cost-effective use of healthcare resources in Singapore's context for the first-line treatment of advanced RCC. The findings from our evaluation will be useful to inform local healthcare decision making and resource allocations for tyrosine kinase inhibitors when appraised alongside comparative clinical effectiveness data and payer affordability considerations.
本研究旨在评估舒尼替尼与干扰素-α治疗新加坡晚期和/或转移性肾细胞癌(RCC)的成本效益。
从医疗保健支付者的角度出发,在 10 年的时间范围内,采用三状态生存模型(无进展、进展疾病和死亡)。对舒尼替尼与干扰素-α的关键试验进行生存曲线外推,以估计潜在的无进展生存和总体生存参数分布。健康状态效用值源自文献,直接成本则来自当地公立医疗机构。模型中的舒尼替尼剂量反映了当地的处方实践,即使用 50mg(28%)和 37.5mg(72%)两种强度的组合。
与干扰素-α相比,舒尼替尼的基础病例分析得出增量成本效益比(ICER)为每获得 1 个质量调整生命年增加 SGD191,061(USD139,757)。敏感性分析表明,ICER 对假设无进展健康状态的效用值和舒尼替尼价格的变化最为敏感。
在没有任何价格降低的情况下,舒尼替尼的 ICER 极高,在新加坡的背景下,不被认为是晚期 RCC 一线治疗中医疗资源的一种具有成本效益的利用。我们的评估结果将有助于为酪氨酸激酶抑制剂提供当地医疗保健决策和资源分配的信息,同时考虑到比较临床疗效数据和支付方的负担能力。