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印度间变性淋巴瘤激酶和 ROS1 融合阳性非小细胞肺癌靶向治疗的经济学评价。

Economic Evaluation of Targeted Therapies for Anaplastic Lymphoma Kinase- and ROS1 Fusion-Positive Non-Small Cell Lung Cancer in India.

机构信息

Department of Community Medicine and School of Public Health, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Department of Radiation Oncology, Government Medical College and Hospital, Chandigarh, India.

出版信息

JCO Glob Oncol. 2024 Feb;10:e2300260. doi: 10.1200/GO.23.00260.

Abstract

PURPOSE

Targeted therapies, such as crizotinib and ceritinib, have shown promising results in treating non-small cell lung cancer (NSCLC) with specific oncogenic drivers like anaplastic lymphoma kinase (), () oncogene, etc. This study aims to assess the cost-effectiveness of these therapies for patients with NSCLC in India.

METHODS

The Markov model consisted of three health states: progression-free survival, progressive disease, and death. Lifetime costs and consequences were estimated for three treatment arms: crizotinib, ceritinib, and chemotherapy for patients with - and -positive NSCLC. Incremental cost per quality-adjusted life-year (QALY) gained with crizotinib and ceritinib was compared to chemotherapy and assessed using a willingness-to-pay threshold of one-time per capita gross domestic product in India.

RESULTS

The total lifetime cost per patient for -positive NSCLC was ₹332,456 ($4,054 US dollars [USD]), ₹1,284,100 ($15,659 USD), and ₹2,337,779 ($28,509 USD) in the chemotherapy, crizotinib, and ceritinib arms, respectively. The mean QALYs lived per patient were 1.20, 2.21, and 3.34, respectively. For patients with -positive NSCLC, the total cost was ₹323,011 ($3,939 USD) and ₹1,763,541 ($21,507 USD) for chemotherapy and crizotinib, with mean QALYs lived per patient of 1.16 and 2.73, respectively. Nearly 92% and 81% reduction in the price of ceritinib and crizotinib is required to make it a cost-effective treatment option for - and -positive NSCLC, respectively.

CONCLUSION

Our study findings suggest that the prices of ceritinib and crizotinib need to be reduced significantly to justify their value for inclusion in India's publicly financed health insurance scheme for treatment of patients with locally advanced/metastatic - and -positive NSCLC, respectively.

摘要

目的

针对具有特定致癌驱动基因(如间变性淋巴瘤激酶 ()、() 癌基因等)的非小细胞肺癌 (NSCLC),靶向治疗药物如克唑替尼和塞瑞替尼已显示出良好的疗效。本研究旨在评估这些疗法在印度 NSCLC 患者中的成本效益。

方法

Markov 模型由三个健康状态组成:无进展生存期、疾病进展和死亡。对于具有 () 阳性和 () 阳性 NSCLC 的患者,分别评估了克唑替尼、塞瑞替尼和化疗三个治疗组的终生成本和结果。使用印度一次性人均国内生产总值 (GDP) 作为意愿支付阈值,比较克唑替尼和塞瑞替尼的增量成本效益比 (QALY)。

结果

() 阳性 NSCLC 患者的总终生治疗费用分别为化疗组 332456 印度卢比($4054 美元)、克唑替尼组 1284100 印度卢比($15659 美元)和塞瑞替尼组 2337779 印度卢比($28509 美元)。每位患者的平均 QALY 分别为 1.20、2.21 和 3.34。对于 () 阳性 NSCLC 患者,化疗组和克唑替尼组的总费用分别为 323011 印度卢比($3939 美元)和 1763541 印度卢比($21507 美元),每位患者的平均 QALY 分别为 1.16 和 2.73。塞瑞替尼和克唑替尼的价格需要分别降低近 92%和 81%,才能使其成为 () 阳性和 () 阳性 NSCLC 的一种具有成本效益的治疗选择。

结论

本研究结果表明,塞瑞替尼和克唑替尼的价格需要大幅降低,才能使其成为印度公共资助的医疗保险计划中治疗局部晚期/转移性 () 阳性和 () 阳性 NSCLC 的一种具有成本效益的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b1c/10881089/1a411744ca4b/go-10-e2300260-g001.jpg

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