HTA and Pharmaceutical Economics Department, Italian Medicines Agency, Via del Tritone 181, 00187, Rome, Italy.
BioDrugs. 2024 Nov;38(6):831-844. doi: 10.1007/s40259-024-00683-0. Epub 2024 Oct 15.
Advanced therapy medicinal products (ATMPs) are an innovative output of biomedical research, characterized by a high level of uncertainty on long-term efficacy and safety, elevated price tags and often complex administration. All these elements compounded make their European authorization, national price negotiation for reimbursement and subsequent dispensation and administration to the patient less straightforward and often less successful than for less innovative drugs. To assess if these hurdles have affected patient access and how are ATMPs used in Italy, we have analysed availability, access and expenditure of ATMPs in the period spanning from 2016 to 2023.
We have analysed real world data on the duration of ATMP regulatory evaluations for authorisation and reimbursement, time to first patient access and expenditure for ATMPs through the Italian National Health System (INHS) expenditure data flow, as well as information on patient mobility and availability of health facilities specialized in administering ATMPs.
Of the 18 ATMPs currently authorized in Europe, 9 are reimbursed by the INHS, but only 6 were actually used, generating a cumulative expenditure of roughly 300 Mln€ from 2016 to 2023, largely owing to CAR-T therapies. Time to patient access reaches an average of 340.6 days from the day publication in the official Gazette of the reimbursement decision to first patient treatment in one of the 107 health facilities authorized for ATMP administration, after an even longer evaluation time by regulatory agencies.
Since the first reimbursement decision for an ATMP in Italy, back in 2016, these innovative drugs became progressively more and more available, both in terms of numbers and in terms of coverage across the country. Almost all Italian regions have at least one centre for ATMP administration and has performed a treatment in 2023. Notwithstanding their high per-treatment prices, ATMPs currently have a rather contained expenditure, however it is bound to keep growing in the next few years.
先进治疗药物产品(ATMPs)是生物医学研究的创新性成果,其长期疗效和安全性具有高度不确定性,价格高昂,且通常给药方式复杂。所有这些因素使得它们在欧洲的授权、国家报销的价格谈判以及随后向患者的配药和给药变得不那么直接,而且往往不如创新药物成功。为了评估这些障碍是否影响了患者的获得途径,以及 ATMP 在意大利的使用情况,我们分析了 2016 年至 2023 年期间 ATMP 的供应、获得途径和支出情况。
我们分析了关于 ATMP 监管评估授权和报销的持续时间、首次患者获得途径的时间以及通过意大利国家卫生系统(INHS)支出数据流程的 ATMP 支出的数据,以及有关患者流动性和专门管理 ATMP 的卫生机构可用性的信息。
在欧洲目前授权的 18 种 ATMP 中,有 9 种由 INHS 报销,但实际上只有 6 种被使用,从 2016 年至 2023 年共产生了约 3 亿欧元的累计支出,这主要归功于嵌合抗原受体 T 细胞(CAR-T)疗法。从报销决定在官方公报上公布到 107 个授权管理 ATMP 的卫生机构中首次对患者进行治疗的第一天,患者获得途径的时间平均为 340.6 天,而监管机构的评估时间更长。
自 2016 年意大利首次作出 ATMP 报销决定以来,这些创新药物在数量上以及在全国范围内的覆盖范围上都变得越来越容易获得。几乎所有意大利地区都至少有一个 ATMP 管理中心,并在 2023 年进行了治疗。尽管每次治疗的单价很高,但 ATMP 目前的支出相当有限,但在未来几年内肯定会继续增长。