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Cost-effectiveness of sunitinib as second-line treatment for gastrointestinal stromal tumor in the People’s Republic of China

机译:舒尼替尼作为胃肠道间质瘤二线治疗的成本效益

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Objective: To evaluate the cost-effectiveness of sunitinib as a second-line treatment in patients with advanced gastrointestinal stromal tumors that no longer respond to imatinib 400 mg/d, compared with imatinib 600 mg/d, 800 mg/d, or best supportive care (BSC) in the People’s Republic of China. Methods: This study was conducted from the government payer’s perspective with a time horizon of 5?years. Three health states were considered: progression-free survival, disease progression survival, and death, with a cycle length of 6?weeks. Probabilities of disease progression and death were estimated based on survival functions using exponential distribution and progression survival data in the clinical trials. Drug costs were based on drug retail prices and the patient assistance program in the People’s Republic of China, and adverse event management costs were based on published data and/or expert opinion. Uncertainties for parameters in the study were addressed through one-way deterministic and probabilistic sensitivity analysis. Results: When sunitinib was compared with imatinib 600?mg/d and BSC, the incremental cost-effectiveness ratio was RMB75,715 with RMB121,080 per quality-adjusted life-year (QALY) gained. Sunitinib demonstrated lower costs and higher QALYs than imatinib 800?mg/d. In the probabilistic sensitivity analysis, the willingness-to-pay per QALY gained was set to be three times the per capita gross domestic product of the People’s Republic of China, that is, RMB46,510 in 2014. Sunitinib was demonstrated to be cost-effective compared with imatinib 600?mg/d, imatinib 800?mg/d, and BSC, with probabilities of 82.3%, 95.6%, and 78.2%, respectively. Limitations: Clinical data for imatinib 800?mg/d and BSC in the analysis were based upon studies in non-Chinese populations. Because of the unavailability of utility data from Chinese gastrointestinal stromal tumor patients, the analysis used the utility estimates from studies performed in other countries. Conclusion: Sunitinib provides greater clinical benefit than high-dose imatinib or BSC as a second-line treatment. In the Chinese setting, sunitinib is estimated to be cost-effective compared with imatinib 800?mg/d, imatinib 600?mg/d, or BSC.
机译:目的:评估舒尼替尼作为二线治疗对不再对伊马替尼400 mg / d,伊马替尼600 mg / d,800 mg / d或最佳支持治疗的晚期胃肠道间质瘤患者的二线治疗的成本效益中华人民共和国(BSC)。方法:本研究是从政府付款方的角度进行的,时间跨度为5年。考虑了三种健康状态:无进展生存期,疾病进展生存期和死亡,周期为6周。在临床试验中使用指数分布和进展生存数据,根据生存功能估算疾病进展和死亡的可能性。药品费用是根据药品零售价格和中华人民共和国的患者救助计划得出的,不良事件管理费用是根据已发布的数据和/或专家意见得出的。通过单向确定性和概率敏感性分析解决了研究中参数的不确定性。结果:将舒尼替尼与伊马替尼600?mg / d和BSC进行比较,增加的成本效益比为75,715元,每质量调整生命年(QALY)获得121,080元。与800毫克/天的伊马替尼相比,舒尼替尼具有更低的成本和更高的QALY。在概率敏感性分析中,将获得的每QALY的支付意愿设为中华人民共和国的人均国内生产总值的三倍,即2014年的人民币46,510元。与伊马替尼600?mg / d,伊马替尼800?mg / d和BSC相比,有效率分别为82.3%,95.6%和78.2%。局限性:分析中伊马替尼800?mg / d和BSC的临床数据基于对非中国人群的研究。由于无法获得中国胃肠道间质瘤患者的效用数据,因此该分析使用了在其他国家进行的研究的效用估计值。结论:舒尼替尼作为二线治疗比大剂量伊马替尼或BSC具有更大的临床益处。在中国,与依马替尼800?mg / d,依马替尼600?mg / d或BSC相比,舒尼替尼被认为具有成本效益。

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