Shu Yamin, Zhang Qilin, He Xucheng, Chen Li
Department of Pharmacy, West China Second University Hospital, Sichuan University, Chengdu, People's Republic of China.
Evidence-Based Pharmacy Center, West China Second University Hospital, Sichuan University, Chengdu, People's Republic of China.
Cancer Manag Res. 2021 Nov 3;13:8297-8306. doi: 10.2147/CMAR.S334643. eCollection 2021.
The aim of this study was to evaluate the cost-effectiveness of gefitinib plus chemotherapy (GCP) versus gefitinib alone for advanced non-small-cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutations in China.
A decision-analytic Markov model was conducted to simulate the disease process of advanced NSCLC patients with EGFR mutations. Three distinct health states: progression-free survival (PFS), progressive disease (PD) and death were included. Clinical data were derived from the NEJ009 study. The cost was evaluated from the perspective of the Chinese society. Quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratios (ICER) were calculated over a 10-year lifetime horizon. One-way sensitivity analysis and probabilistic sensitivity analysis were also performed to explore the uncertainty of parameters in the study.
The base case analysis demonstrated that gefitinib plus chemotherapy gained 2.44 QALYs at an average cost of $59,571.34, while the effectiveness and cost of gefitinib group were 1.82 QALYs and $52,492.75, respectively. The ICER for gefitinib plus chemotherapy was $11,499.98 per QALY gained. The ICER was lower than the accepted willingness-to-pay (WTP) threshold, which was three times gross domestic product (GDP) per capita of China ($31,498.70 per QALY). Variation of parameters did not reverse the cost-effectiveness of gefitinib plus chemotherapy through univariable and probabilistic sensitivity analyses.
Our results showed that gefitinib plus chemotherapy is a cost-effective treatment option compared with gefitinib for advanced NSCLC patients with EGFR mutations in China.
本研究旨在评估在中国,吉非替尼联合化疗(GCP)与单用吉非替尼治疗表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌(NSCLC)患者的成本效益。
采用决策分析马尔可夫模型模拟EGFR突变的晚期NSCLC患者的疾病进程。纳入三个不同的健康状态:无进展生存期(PFS)、疾病进展(PD)和死亡。临床数据来源于NEJ009研究。从中国社会角度评估成本。在10年的生存期内计算质量调整生命年(QALYs)和增量成本效益比(ICER)。还进行了单因素敏感性分析和概率敏感性分析,以探讨研究中参数的不确定性。
基础病例分析表明,吉非替尼联合化疗获得2.44个QALYs,平均成本为59,571.34美元,而吉非替尼组的有效性和成本分别为1.82个QALYs和52,492.75美元。吉非替尼联合化疗的ICER为每获得一个QALY 11,499.98美元。该ICER低于可接受的支付意愿(WTP)阈值,即中国人均国内生产总值的三倍(每QALY 31,498.70美元)。通过单变量和概率敏感性分析,参数变化并未改变吉非替尼联合化疗的成本效益。
我们的结果表明,在中国,对于EGFR突变的晚期NSCLC患者,与单用吉非替尼相比,吉非替尼联合化疗是一种具有成本效益的治疗选择。