Cost-Effectiveness Analysis of Bevacizumab Biosimilars Versus Originator Bevacizumab for Metastatic Colorectal Cancer: A Comparative Study Using Real-World Data.

IF 4.9 2区 医学 Q1 ECONOMICS
Brandon Lu, Erind Dvorani, Lena Nguyen, Jaclyn M Beca, Rebecca E Mercer, Andrea Adamic, Caroline Muñoz, Kelvin K W Chan
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引用次数: 0

Abstract

Objectives: MVASI (Amgen) and Zirabev (Pfizer) are 2 of the earliest bevacizumab biosimilars approved for the first-line treatment of metastatic colorectal cancer (mCRC). We aimed to confirm and quantify the real-world cost savings and cost-effectiveness of MVASI and Zirabev relative to originator bevacizumab for patients with mCRC.

Methods: We conducted a population-based, retrospective cohort study in Ontario, Canada, where originator and biosimilar bevacizumab are universally publicly funded. All mCRC patients who received originator bevacizumab between January 2008 and August 2019 or biosimilar bevacizumab between August 2019 and March 2021 were propensity score matched (1:4) to adjust for baseline differences. Total 1-year patient-level costs (CAD) and effects (life years [LY] and quality-adjusted LYs) were calculated from the public health payer's perspective. Primary outcomes included incremental net monetary benefit and incremental net health benefit (INHB). Sensitivity analyses included a subgroup analysis by biosimilar type (MVASI/Zirabev) and a 2-year analysis.

Results: The matched cohort included 747 biosimilar cases and 2945 comparators. Bevacizumab biosimilars were associated with an incremental cost of -$6379 (95%CI: -9417, -3537) (ie, cost saving) and incremental effect of 0.0 (95% CI: -0.02, 0.02) LY and -0.01 (95% CI: -0.03, 0) quality-adjusted LYs gained. Incremental net monetary benefit and INHB estimates were $6331 (95% CI: 6245, 6417) and 0.127 LY (95% CI: 0.125, 0.128), respectively, at a willingness-to-pay threshold of $50 000/life year gained, with all estimates indicating the cost-effectiveness of biosimilar bevacizumab. Cost-effectiveness remained consistent across biosimilar brand subgroups and 2-year sensitivity analyses.

Conclusion: Bevacizumab biosimilars demonstrated real-world cost savings while providing similar survival benefit as originator bevacizumab, confirming the initial expectations of their implementation and supporting health system sustainability.

贝伐珠单抗生物仿制药与原研贝伐珠单抗治疗转移性结直肠癌的成本效益分析:一项使用真实世界数据的比较研究。
目的:MVASI(安进公司)和Zirabev(辉瑞公司)是最早获准用于转移性结直肠癌(mCRC)一线治疗的两种贝伐珠单抗生物仿制药。我们的目的是确认和量化 MVASI 和 Zirabev 相对于原研贝伐珠单抗治疗 mCRC 患者的实际成本节约和成本效益:我们在加拿大安大略省开展了一项基于人群的回顾性队列研究,该省的原研药和生物仿制药贝伐珠单抗均由政府资助。对 2008 年 1 月至 2019 年 8 月期间接受原研贝伐珠单抗治疗或 2019 年 8 月至 2021 年 3 月期间接受生物类似物贝伐珠单抗治疗的所有 mCRC 患者进行倾向评分匹配(1:4),以调整基线差异。从公共卫生支付方的角度计算了1年患者层面的总成本(CAD)和效果(生命年(LY)和质量调整生命年(QALY))。主要结果包括增量净货币效益(INMB)和增量净健康效益(INHB)。敏感性分析包括按生物类似药类型(MVASI/Zirabev)进行的亚组分析和两年分析:匹配队列包括 747 个生物类似药病例和 2,945 个比较者。贝伐珠单抗生物仿制药的增量成本为-6,379美元(95%CI:-9,417, -3,537)(即节省成本),增量效果为0.0(95%CI:-0.02, 0.02)LY和-0.01(95%CI:-0.03, 0)QALY。在 50,000 美元/LYG 的支付意愿阈值下,INMB 和 INHB 的估计值分别为 6,331 美元(95% CI:6,245, 6,417)和 0.127 LY(95% CI:0.125, 0.128),所有估计值均表明生物类似药贝伐珠单抗具有成本效益。在生物类似药品牌亚组和2年敏感性分析中,成本效益保持一致:贝伐珠单抗生物仿制药在提供与原研药贝伐珠单抗相似的生存获益的同时,还显示出了实际的成本节约效果,证实了最初对其实施的预期,并支持了医疗系统的可持续性。
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来源期刊
Value in Health
Value in Health 医学-卫生保健
CiteScore
6.90
自引率
6.70%
发文量
3064
审稿时长
3-8 weeks
期刊介绍: Value in Health contains original research articles for pharmacoeconomics, health economics, and outcomes research (clinical, economic, and patient-reported outcomes/preference-based research), as well as conceptual and health policy articles that provide valuable information for health care decision-makers as well as the research community. As the official journal of ISPOR, Value in Health provides a forum for researchers, as well as health care decision-makers to translate outcomes research into health care decisions.
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