Cost-effectiveness analysis of osimertinib plus chemotherapy for patients with EGFR-mutated advanced non-small cell lung cancer

IF 2.9 2区 医学 Q2 ONCOLOGY Cancer Medicine Pub Date : 2024-08-29 DOI:10.1002/cam4.70083
Wentao Tian, Lishui Niu, Rongrong Zhou, Ziqi Wang, Jiaoyang Ning, Ruoyu Lu, Yin Shi, Zhaohua Tan
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Abstract

Introduction

First-line osimertinib plus chemotherapy significantly prolonged progression-free survival of patients with EGFR-mutated advanced non-small cell lung cancer (NSCLC) compared to osimertinib, according to the FLAURA2 trial.

Methods

We established a Markov model to compare the cost-effectiveness of osimertinib plus chemotherapy with that of osimertinib alone. Clinical data were obtained from the FLAURA and FLAURA2 trials, and additional data were extracted from online resources and publications. Sensitivity analyses were conducted to evaluate the robustness of the findings. We used A willingness-to-pay threshold of $150,000 per quality-adjusted life-years (QALYs) gained. The main outcomes were QALYs, overall costs, incremental cost-effectiveness ratio (ICER), incremental net monetary benefit, and incremental net health benefit. Subgroup analyses were conducted according to patients' mutation type and central nervous system (CNS) metastatic status.

Results

In a 20-year time horizon, the ICER of osimertinib plus chemotherapy versus osimertinib alone was $223,727.1 per QALY gained. The sensitivity analyses identified the cost of osimertinib and the hazard ratio for overall survival as the top 2 influential factors and a 1.9% probability of osimertinib plus chemotherapy to be cost-effective. The subgroup analyses revealed ICERs of $132,614.1, $224,449.8, $201,464.1, and $130,159.7 per QALY gained for L858R mutations, exon 19 deletions, CNS metastases, and no CNS metastases subgroups, respectively.

Conclusions

From the perspective of the United States health care system, osimertinib plus chemotherapy is not cost-effective compared to osimertinib alone for treatment-naïve patients with EGFR-mutated advanced NSCLC, but more favorable cost-effectiveness occurs in patients with L858R mutations and patients without baseline CNS metastases.

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奥希替尼联合化疗治疗表皮生长因子受体突变晚期非小细胞肺癌患者的成本效益分析
简介:根据FLAURA2试验,与奥希替尼相比,一线奥希替尼联合化疗可显著延长表皮生长因子受体(EGFR)突变晚期非小细胞肺癌(NSCLC)患者的无进展生存期。 方法 我们建立了一个马尔可夫模型来比较奥希替尼联合化疗与奥希替尼单药的成本效益。临床数据来自 FLAURA 和 FLAURA2 试验,其他数据来自在线资源和出版物。我们进行了敏感性分析,以评估研究结果的稳健性。我们采用的支付意愿阈值为每获得质量调整生命年 (QALY) 150,000 美元。主要结果包括 QALYs、总成本、增量成本效益比 (ICER)、增量净货币效益和增量净健康效益。根据患者的突变类型和中枢神经系统(CNS)转移状态进行了分组分析。 结果 在20年的时间跨度内,奥希替尼联合化疗与奥希替尼单药相比,每QALY收益的ICER为223,727.1美元。敏感性分析发现,奥希替尼的成本和总生存期危险比是前两个影响因素,奥希替尼联合化疗具有成本效益的概率为 1.9%。亚组分析显示,L858R突变、外显子19缺失、中枢神经系统转移和无中枢神经系统转移亚组每QALY收益的ICER分别为132,614.1美元、224,449.8美元、201,464.1美元和130,159.7美元。 结论 从美国医疗系统的角度来看,对于表皮生长因子受体(EGFR)突变的晚期 NSCLC 患者,奥希替尼联合化疗与奥希替尼单药相比并不具有成本效益,但对于 L858R 突变患者和无基线 CNS 转移的患者,成本效益更为有利。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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