Cost-effectiveness Analysis in the New Era of Treatment Strategies in Metastatic Urothelial Carcinoma Based on Checkmate-901 and EV302/Keynote-A39.

IF 8.3 1区 医学 Q1 ONCOLOGY
Constantin Rieger, Jörg Schlüchtermann, Michaela Lehmann, Enno Storz, Richard Weiten, Christian Bach, David Pfister, Axel Heidenreich
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引用次数: 0

Abstract

Background and objective: Metastatic urothelial carcinoma (mUCa) ranks as the costliest cancer to treat per patient due to frequent interventions and expensive follow-ups. Investigating first-line therapies, combinations such as enfortumab vedotin + pembrolizumab (EV + P) and gemcitabine/cisplatin + nivolumab exhibit significant overall survival benefits compared with the standard treatment (SoC; gemcitabine/cisplatin). Here, we conducted a cost-effectiveness analysis for mUCa.

Methods: We developed a Markov model from a payer perspective, filtering clinical data from the phase 3 Checkmate-901 and EV302/Keynote-A39 trials. Monte Carlo simulation was used to identify the optimal treatment from a socioeconomic perspective in Germany and the USA. Finally, we compared the incremental cost-effectiveness ratio (ICER) of each modality at different willingness-to-pay (WTP) thresholds.

Key findings and limitations: At a lifetime horizon, SoC, gemcitabine/cisplatin + nivolumab, and EV + P were associated with average costs of €163 424 (USA: $458 006), €206 853 (USA: $597 802), and €401 170 (USA: $1 228 455), and gained quality-adjusted life years (QALYs) of 1.21, 1.71, and 2.31, respectively. The ICERs of the newer strategies were €87 340 (USA: $281 142; gemcitabine/cisplatin + nivolumab) and €216 140 (USA: $700 448; EV + P). At a commonly used WTP threshold of €/$100 000, gemcitabine/cisplatin + nivolumab would be the optimal strategy in Germany, while EV + P would require a price reduction of 46% (USA: 82%) to be cost effective.

Conclusions and clinical implications: QALYs nearly double with EV + P compared with the current SoC; yet, current costs may not be justified from a strict socioeconomic perspective. Despite its lower oncological benefit, gemcitabine/cisplatin + nivolumab should be considered for first-line therapy due to favorable cost effectiveness, especially in Europe. Establishing individual risk factors is essential for optimizing therapeutic response and treatment costs in the future.

Patient summary: This report presents a cost-effectiveness analysis of emerging treatment options for metastatic urothelial carcinoma. The combination of enfortumab vedotin + pembrolizumab emerged as the most effective treatment; however, it also proved to be the costliest. From a purely socioeconomic standpoint, the combination of gemcitabine/cisplatin and nivolumab represents a cost-effective alternative at least in Germany.

基于Checkmate-901和EV302/Keynote-A39的转移性尿路上皮癌治疗策略新时代的成本效益分析。
背景和目的:由于频繁的干预和昂贵的随访,转移性尿路上皮癌(mUCa)是每位患者治疗成本最高的癌症。在对一线疗法的研究中,与标准疗法(SoC;吉西他滨/顺铂)相比,恩福单抗-维多汀+pembrolizumab(EV+P)和吉西他滨/顺铂+nivolumab等组合疗法显示出显著的总生存获益。在此,我们对mUCa进行了成本效益分析:我们从支付方的角度开发了一个马尔可夫模型,过滤了来自 3 期 Checkmate-901 和 EV302/Keynote-A39 试验的临床数据。从德国和美国的社会经济角度出发,我们使用蒙特卡罗模拟确定了最佳治疗方案。最后,我们比较了每种模式在不同支付意愿(WTP)阈值下的增量成本效益比(ICER):在终生范围内,SoC、吉西他滨/顺铂 + nivolumab 和 EV + P 的平均成本分别为 163 424 欧元(美国:458 006 美元)、206 853 欧元(美国:597 802 美元)和 401 170 欧元(美国:1 228 455 美元),获得的质量调整生命年 (QALY) 分别为 1.21、1.71 和 2.31。较新策略的 ICER 分别为 87 340 欧元(美国:281 142 美元;吉西他滨/顺铂 + nivolumab)和 216 140 欧元(美国:700 448 美元;EV + P)。按照常用的 WTP 临界值 100 000 欧元/美元计算,吉西他滨/顺铂 + nivolumab 将是德国的最佳策略,而 EV + P 则需要降价 46%(美国:82%)才具有成本效益:与目前的 SoC 相比,EV + P 的 QALY 几乎翻了一番;然而,从严格的社会经济角度来看,目前的成本可能并不合理。尽管吉西他滨/顺铂+nivolumab的肿瘤学效益较低,但由于其良好的成本效益,尤其是在欧洲,仍应考虑将其用于一线治疗。患者摘要:本报告对转移性尿路上皮癌的新兴治疗方案进行了成本效益分析。恩福单抗-维多汀+pembrolizumab联合疗法是最有效的治疗方法,但也被证明是最昂贵的治疗方法。单纯从社会经济角度来看,吉西他滨/顺铂和 nivolumab 的组合至少在德国是一种具有成本效益的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
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