在日本,Atezolizumab 与 Durvalumab 作为广泛病变小细胞肺癌患者一线化疗联合疗法的成本效益比较。

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2024-10-01 Epub Date: 2024-09-21 DOI:10.1007/s40261-024-01383-x
Munenobu Kashiwa, Miho Tsukada, Ryo Matsushita
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引用次数: 0

摘要

背景和目的:最近的试验表明,免疫检查点抑制剂(ICIs)、atezolizumab 和 durvalumab 与化疗联合使用可有效治疗广泛病变小细胞肺癌(ED-SCLC)。然而,由于 ICIs 价格昂贵,因此出现了资金问题。为了帮助日本制定公共卫生政策,我们研究了 ICI 与卡铂加依托泊苷(CE)联合治疗作为 ED-SCLC 患者一线疗法的成本效益:方法:使用 IMpower 133 和 CASPIAN 数据创建了一个分区生存模型。方法:使用 IMpower 133 和 CASPIAN 数据创建了分区生存模型,并考虑了医疗费用和质量调整生命年 (QALY)。分析期限、贴现率和阈值分别定为 20 年、2% 和每 QALY 1,500 万日元 [114,068 美元]。增量成本效益比 (ICER) 的计算方法是从已发表的报告中收集合理的参数,并使用参数模型将成本和效果结合起来。采用蒙特卡罗模拟、情景分析和单向敏感性分析来量化不确定性:结果:在比较了阿特珠单抗+CE(ACE)和德伐卢单抗+CE(DCE)与CE后,发现ICER超过了阈值,分别为每QALY 35,048,299日元(266,527美元)和36,665,583日元(278,826美元)。在单向敏感性和情景评估中,即使对参数进行了大幅调整,ICER 也超过了阈值。在概率敏感性分析中,ICI联合化疗的ICER不可能低于阈值:结论:在日本,作为 ED-SCLC 的一线疗法,ACE 和 DCE 与 CE 相比不具成本效益。这两种疗法的 ICER 都很高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Cost-Effectiveness of Atezolizumab Versus Durvalumab as First-Line Combination Treatment with Chemotherapy for Patients with Extensive-Disease Small-Cell Lung Cancer in Japan.

BACKGROUND AND OBJECTIVE: Recent trials have shown that immune checkpoint inhibitors (ICIs), atezolizumab and durvalumab, in combination with chemotherapy, are effective in treating extensive-disease small-cell lung cancer (ED-SCLC). However, owing to the expensiveness of ICIs, monetary issues arise. The cost-effectiveness of ICI combination treatment with carboplatin plus etoposide (CE) as first-line therapy for patients with ED-SCLC was examined to aid public health policy in Japan.

Methods: IMpower 133 and CASPIAN data were used to create a partitioned survival model. Medical expenses and quality-adjusted life years (QALYs) were considered. The analysis period, discount rate, and threshold were set at 20 years, 2%, and 15 million Japanese yen (JPY) [114,068 US dollars (USD)] per QALY, respectively. The incremental cost-effectiveness ratio (ICER) was calculated by gathering reasonable parameters from published reports and combining the costs and effects using parametric models. Monte Carlo simulations, scenario analysis, and one-way sensitivity analyses were employed to quantify uncertainty.

Results: After comparing atezolizumab plus CE (ACE) and durvalumab plus CE (DCE) with CE, it was found that the ICERs exceeded the threshold at 35,048,299 JPY (266,527 USD) and 36,665,583 JPY (278,826 USD) per QALY, respectively. For one-way sensitivity and scenario assessments, the ICERs exceeded the threshold, even with considerably adjusted parameters. For the probabilistic sensitivity analyses, there was no probability that the ICER of the ICI combination treatment with chemotherapy would fall below the threshold.

Conclusion: ACE and DCE were not cost-effective compared with CE as first-line therapy for ED-SCLC in Japan. Both these therapies exhibited high ICERs.

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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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