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基于 JASPAC-01 试验的可切除胰腺癌中 S-1 或吉西他滨辅助治疗的成本效益分析。

S-1 or gemcitabine adjuvant therapy in resected pancreatic cancer: a cost-effectiveness analysis based on the JASPAC-01 trial.

机构信息

Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.

West China Biomedical Big Data Center, Sichuan University, Chengdu, China.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2020 Feb;20(1):133-138. doi: 10.1080/14737167.2020.1677155. Epub 2019 Oct 10.

DOI:10.1080/14737167.2020.1677155
PMID:31597496
Abstract

: This study aimed to investigate the cost-effectiveness of adjuvant treatments in resected pancreatic cancer.: A Markov model was developed to mimic the disease process of postoperative pancreatic cancer, encompassing three health states (relapse-free survival, recurrent disease, and death). Health outcomes and utility scores were derived from the phase III trial and available literature. Cost data were calculated using standard fee data from the West China Hospital for 2017. One-way sensitivity analyses and probabilistic sensitivity analyses were developed to explore model uncertainty.: Treatment with S-1 was estimated to yield 1.61 quality-adjusted life-years (QALYs) at a cost of $25,696, whereas treatment with gemcitabine yielded 1.27 QALYs at a cost of $28,930. The incremental cost-effectiveness ratio of S-1 versus gemcitabine was $-9,490 per QALY. Based on the willingness-to-pay threshold of $25,841 per QALY, the net monetary benefit (NMB) was $15,786 for S-1 and $3,727 for gemcitabine, generating the incremental NMB of $12,059. A probabilistic sensitivity analysis revealed that the probabilities of S-1 and gemcitabine being cost-effective were 92% and 8%, respectively. Results were robust to changes in parameters.: Adjuvant therapy using S-1 is a cost-effective alternative compared to gemcitabine in patients with postoperative pancreatic cancer from the Chinese societal perspective.

摘要

: 本研究旨在探讨辅助治疗在可切除胰腺癌中的成本效益。: 建立了一个马尔可夫模型来模拟术后胰腺癌的疾病过程,包括三种健康状态(无复发生存、复发疾病和死亡)。健康结果和效用评分来自 III 期试验和现有文献。成本数据使用 2017 年华西医院的标准费用数据计算。进行了单因素敏感性分析和概率敏感性分析,以探讨模型的不确定性。: S-1 治疗估计可获得 1.61 个质量调整生命年(QALY),成本为 25696 美元,而吉西他滨治疗可获得 1.27 个 QALY,成本为 28930 美元。S-1 与吉西他滨相比,增量成本效益比为每 QALY 负 9490 美元。根据每 QALY 25841 美元的支付意愿阈值,S-1 的净货币收益(NMB)为 15786 美元,吉西他滨为 3727 美元,S-1 的增量 NMB 为 12059 美元。概率敏感性分析显示,S-1 和吉西他滨具有成本效益的概率分别为 92%和 8%。结果对参数变化具有稳健性。: 从中国社会的角度来看,与吉西他滨相比,术后胰腺癌患者使用 S-1 进行辅助治疗是一种具有成本效益的替代方案。

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