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临近专利到期的“常青化”策略对生物类似药的采用和公共医疗保健成本的影响:以荷兰引入曲妥珠单抗第二种给药形式为例的研究

The impact of an 'evergreening' strategy nearing patent expiration on the uptake of biosimilars and public healthcare costs: a case study on the introduction of a second administration form of trastuzumab in The Netherlands.

机构信息

NZa, Utrecht, The Netherlands.

Erasmus University Rotterdam, Rotterdam, The Netherlands.

出版信息

Eur J Health Econ. 2024 Sep;25(7):1147-1163. doi: 10.1007/s10198-023-01648-w. Epub 2024 Jan 8.

Abstract

In this paper, we explore dynamic market share and public healthcare costs of trastuzumab's evergreening (subcutaneous) variant during introduction of trastuzumab's competitive biosimilar variants in the Netherlands. We used a time series design to assess dynamic market share of trastuzumab's evergreening variant after introducing trastuzumab's biosimilar variants, focusing on the number of treatments and patients. The public healthcare costs of this evergreening strategy were estimated using administrative claims data. Our results show that the original trastuzumab was completely replaced by the subcutaneous and biosimilar variants. The uptake of the subcutaneous form peaked at 50% market share but after the introduction of biosimilars progressively reduced to a market share of 20%, resulting in a more competitive market structure. The public healthcare costs for trastuzumab significantly decreased after the introduction of the biosimilars. After the introduction of the biosimilars, a substantial price drop is visible, with the subcutaneous version, still under patent, also falling sharply in price but less strongly than the iv/biosimilar version. As the costs are publicly funded, we recommend a more explicit societal debate to consider if the potential benefits of subcutaneous Herceptin (and other similar medicines) are worth the additional costs, and at which price it should be reimbursed as the part of the benefit package.

摘要

在本文中,我们探讨了在荷兰引入曲妥珠单抗竞争生物类似药变体时,曲妥珠单抗的专利延期(皮下)变体的动态市场份额和公共医疗保健成本。我们使用时间序列设计来评估引入曲妥珠单抗生物类似药变体后曲妥珠单抗专利延期变体的动态市场份额,重点关注治疗次数和患者数量。使用管理索赔数据估算了这种专利延期策略的公共医疗保健成本。我们的研究结果表明,原始曲妥珠单抗已被皮下制剂和生物类似药完全取代。皮下制剂的使用率达到了 50%的市场份额峰值,但在生物类似药推出后逐渐下降至 20%,从而形成了更具竞争力的市场结构。引入生物类似药后,曲妥珠单抗的公共医疗保健成本显著降低。在引入生物类似药后,价格明显下降,尽管仍受专利保护的皮下制剂价格也大幅下降,但降幅不及静脉注射/生物类似药版本。由于成本由公共资金支付,我们建议进行更明确的社会辩论,以考虑皮下赫赛汀(和其他类似药物)的潜在益处是否值得额外的成本,以及应该以何种价格将其作为福利计划的一部分进行报销。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bafb/11377641/f4508f0f5f02/10198_2023_1648_Fig1_HTML.jpg

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