Shu Yamin, Ding Yiling, Li Feie, Zhang Qilin
Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo 113-0033, Japan.
Int Immunopharmacol. 2023 Jan;114:109589. doi: 10.1016/j.intimp.2022.109589. Epub 2022 Dec 19.
First-line treatment with nivolumab plus ipilimumab has been shown to improve overall survival (OS) and progression-free survival (PFS) for patients with advanced non-small cell lung cancer (NSCLC). The current study evaluated the cost-effectiveness of nivolumab plus ipilimumab versus chemotherapy in advanced NSCLC from the perspective of Chinese healthcare system.
A three state-transition Markov model was employed to evaluate the cost and effectiveness of nivolumab plus ipilimumab versus chemotherapy in the first-line treatment of advanced NSCLC. Key clinical data in the model were derived from Part 1 of the phase 3 CheckMate 227 trial (NCT02477826). Costs and utilities were obtained from published literatures. The main endpoints of the model were costs, quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratio (ICER). One-way and probabilistic sensitivity analyses were performed to assess the model uncertainty.
Nivolumab plus ipilimumab was associated with an increase in overall cost of $95,867.82 and improved effectiveness of 0.98 QALYs compared with chemotherapy, yielding an ICER of $97,676.24 per QALY. In one-way sensitivity analysis, the variables that had the greatest influence on the ICER were hazard ratio for OS and body weight. In probabilistic analysis, nivolumab plus ipilimumab had a 0% probability of being cost-effective at a willingness-to-pay (WTP) threshold of $37,663.26/QALY in China. However, the combination therapy would become cost-effective when the cost of nivolumab and ipilimumab were discounted by 65%.
First-line nivolumab plus ipilimumab treatment for advanced NSCLC was found to be not cost-effective compared with chemotherapy at a WTP threshold of $37,663.26/QALY in China.
已证明纳武利尤单抗联合伊匹木单抗一线治疗可改善晚期非小细胞肺癌(NSCLC)患者的总生存期(OS)和无进展生存期(PFS)。本研究从中国医疗保健系统的角度评估了纳武利尤单抗联合伊匹木单抗与化疗相比在晚期NSCLC中的成本效益。
采用三状态转换马尔可夫模型评估纳武利尤单抗联合伊匹木单抗与化疗在晚期NSCLC一线治疗中的成本和效果。模型中的关键临床数据来自3期CheckMate 227试验(NCT02477826)的第1部分。成本和效用值来自已发表的文献。模型的主要终点是成本、质量调整生命年(QALY)和增量成本效益比(ICER)。进行单向和概率敏感性分析以评估模型的不确定性。
与化疗相比,纳武利尤单抗联合伊匹木单抗使总成本增加95,867.82美元,效果改善0.98 QALY,ICER为每QALY 97,676.24美元。在单向敏感性分析中,对ICER影响最大的变量是OS的风险比和体重。在概率分析中,在中国支付意愿(WTP)阈值为37,663.26美元/QALY时,纳武利尤单抗联合伊匹木单抗具有成本效益的概率为0%。然而,当纳武利尤单抗和伊匹木单抗的成本降低65%时,联合治疗将具有成本效益。
在中国支付意愿阈值为37,663.26美元/QALY时,与化疗相比,纳武利尤单抗联合伊匹木单抗一线治疗晚期NSCLC不具有成本效益。