McGill University Health Center, Montreal, QC, Canada.
McMaster University, Hamilton, ON, Canada.
Clin Drug Investig. 2018 Dec;38(12):1155-1165. doi: 10.1007/s40261-018-0705-6.
The development of new targeted therapies in kidney cancer has shaped disease management in the metastatic phase. Our study aims to conduct a cost-utility analysis of sunitinib versus pazopanib in first-line setting in Canada for metastatic renal cell carcinoma (mRCC) patients using real-world data.
A Markov model with Monte-Carlo microsimulations was developed to estimate the clinical and economic outcomes of patients treated in first-line with sunitinib versus pazopanib. Transition probabilities were estimated using observational data from a Canadian database where real-life clinical practice was captured. The costs of therapies, disease progression, and management of adverse events were included in the model in Canadian dollars ($Can). Utility and disutility values were included for each health state. Incremental cost-utility ratio (ICUR) and incremental cost-effectiveness ratios (ICER) were calculated for a time horizon of 5 years, from the Canadian Healthcare System perspective.
The cost difference was $36,303 and the difference in quality-adjusted life year (QALY) was 0.54 in favour of sunitinib with an ICUR of $67,227/QALY for sunitinib versus pazopanib. The major cost component (56%) is related to best supportive care (BSC) where patients tend to stay for a longer period of time compared to other states. The difference in life years gained (LYG) between sunitinib and pazopanib was 1.21 LYG (33.51 vs 19.03 months) and the ICER was $30,002/LYG. Sensitivity analysis demonstrated the robustness of the model with a high probability of sunitinib being a cost-effective option when compared to pazopanib.
When using real-world evidence, sunitinib is found to be a cost-effective treatment compared to pazopanib in mRCC patients in Canada.
在转移性肾细胞癌(mRCC)中,新型靶向治疗的发展改变了疾病的治疗管理模式。本研究旨在使用真实世界的数据,对加拿大转移性肾细胞癌患者一线使用舒尼替尼与帕唑帕尼的成本-效用进行分析。
采用 Markov 模型结合蒙特卡罗微模拟方法,估算一线使用舒尼替尼与帕唑帕尼治疗的患者的临床和经济结局。使用加拿大数据库中的观察性数据估算转移概率,该数据库记录了真实的临床实践。模型中纳入了治疗、疾病进展和不良事件管理的成本,以加元(CAD)计价。模型纳入了每个健康状态的效用和失效率值。从加拿大医疗保健系统的角度出发,对 5 年时间内的增量成本-效用比(ICUR)和增量成本-效果比(ICER)进行了计算。
舒尼替尼的成本差异为 36,303 CAD,质量调整生命年(QALY)差异为 0.54,舒尼替尼的增量成本-效用比(ICUR)为 67,227 CAD/QALY,优于帕唑帕尼。主要成本构成部分(56%)与最佳支持治疗(BSC)相关,与其他状态相比,患者在 BSC 中停留的时间往往更长。舒尼替尼与帕唑帕尼相比,生命年增加(LYG)差异为 1.21 LYG(33.51 个月与 19.03 个月),ICER 为 30,002 CAD/LYG。敏感性分析表明,该模型具有稳健性,与帕唑帕尼相比,舒尼替尼具有较高的成本效益的可能性。
使用真实世界证据时,在加拿大的转移性肾细胞癌患者中,与帕唑帕尼相比,舒尼替尼是一种具有成本效益的治疗方法。