Institute of Medical Information, Chinese Academy of Medical Sciences, Beijing, China.
China Health Economics Association, Beijing, China.
PLoS One. 2022 Jun 24;17(6):e0270118. doi: 10.1371/journal.pone.0270118. eCollection 2022.
The aim of this study was to evaluate the cost-effectiveness of durvalumab compared with Best supportive care (BSC) after chemoradiotherapy in patients with stage III non-small cell lung cancer from healthcare system perspective in China.
A dynamic state transition model was adopted to simulate life time, direct medical costs and QALYs. In the base case scenario, for patients with unresectable, stage Ⅲ non-small cell lung cancer whose disease has not progressed after platinum-based chemoradiation therapy, the treatment group would use durvalumab whereas the control group would use BSC. Clinical data and health utility were derived from the patient-level data of Asian ethnicity in the PACIFIC trial. Cost of drug acquisition, follow-up, medical service, inspection, terminal care and adverse event treatment were considered in this model. The cost of durvalumab was calculated based on retail prices and Patient Assistance Program.
In the base case, the durvalumab group yielded an additional 2.60 LYs and 2.37QALYs (discounted), causing an additional cost of 0.459 million RMB and 0.109 million RMB without and with PAP, so the ICER was 193,898 RMB/QALY and 46,093.12 RMB/QALY respectively.
This study demonstrated that durvalumab can improve the survival of patients with unresectable, stage Ⅲ non-small cell lung cancer whose disease has not progressed after platinum-based chemoradiation therapy and would be a cost-effective option compared with BSC at a willingness to pay (WTP) threshold of 212676 RMB (three times GDP per capita of China in 2019).
本研究旨在评估 durvalumab 与最佳支持治疗(BSC)相比在接受放化疗后的 III 期非小细胞肺癌患者中的成本效益,从中国医疗保健系统的角度出发。
采用动态状态转移模型来模拟生存期、直接医疗成本和 QALYs。在基础病例中,对于放化疗后疾病未进展的不可切除的 III 期非小细胞肺癌患者,治疗组使用 durvalumab,对照组使用 BSC。临床数据和健康效用来自 PACIFIC 试验中亚洲人种患者的个体数据。该模型考虑了药物获取、随访、医疗服务、检查、终末期护理和不良事件治疗的成本。durvalumab 的成本是根据零售价格和患者援助计划计算的。
在基础病例中,durvalumab 组增加了 2.60 个生命年和 2.37 个 QALYs(折扣后),导致无 PAP 时额外增加 45.9 万人民币和有 PAP 时额外增加 10.9 万人民币的成本,因此增量成本效益比(ICER)分别为 193898 人民币/QALY 和 46093.12 人民币/QALY。
本研究表明,durvalumab 可提高放化疗后疾病未进展的不可切除的 III 期非小细胞肺癌患者的生存,并在 212676 人民币(2019 年中国人均 GDP 的三倍)的支付意愿(WTP)阈值下,与 BSC 相比具有成本效益。