Institute for Cancer Research, Oslo University Hospital and Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Department of Medical Oncology, Leiden University Medical Centre, Leiden, The Netherlands.
Acta Oncol. 2024 May 23;63:385-391. doi: 10.2340/1651-226X.2024.34791.
In the two European Union (EU)-funded projects, PCM4EU (Personalized Cancer Medicine for all EU citizens) and PRIME-ROSE (Precision Cancer Medicine Repurposing System Using Pragmatic Clinical Trials), we aim to facilitate implementation of precision cancer medicine (PCM) in Europe by leveraging the experience from ongoing national initiatives that have already been particularly successful.
PCM4EU and PRIME-ROSE gather 17 and 24 partners, respectively, from 19 European countries. The projects are based on a network of Drug Rediscovery Protocol (DRUP)-like clinical trials that are currently ongoing or soon to start in 11 different countries, and with more trials expected to be established soon. The main aims of both the projects are to improve implementation pathways from molecular diagnostics to treatment, and reimbursement of diagnostics and tumour-tailored therapies to provide examples of best practices for PCM in Europe.
PCM4EU and PRIME-ROSE were launched in January and July 2023, respectively. Educational materials, including a podcast series, are already available from the PCM4EU website (http://www.pcm4eu.eu). The first reports, including an overview of requirements for the reimbursement systems in participating countries and a guide on patient involvement, are expected to be published in 2024.
PCM4EU and PRIME-ROSE were launched in January and July 2023, respectively. Educational materials, including a podcast series, are already available from the PCM4EU website (http://www.pcm4eu.eu). The first reports, including an overview of requirements for the reimbursement systems in participating countries and a guide on patient involvement, are expected to be published in 2024.
European collaboration can facilitate the implementation of PCM and thereby provide affordable and equitable access to precision diagnostics and matched therapies for more patients.
在欧盟(EU)资助的两个项目 PCM4EU(为所有欧盟公民提供个性化癌症医学)和 PRIME-ROSE(利用已经特别成功的正在进行的国家倡议的经验来促进欧洲精准癌症医学的实施)中,我们旨在通过利用已经特别成功的正在进行的国家倡议的经验,促进欧洲精准癌症医学(PCM)的实施。
PCM4EU 和 PRIME-ROSE 分别汇集了来自 19 个欧洲国家的 17 个和 24 个合作伙伴。这两个项目都是基于一个类似药物再发现方案(DRUP)的临床试验网络,该网络目前正在 11 个不同的国家进行或即将开始,并且预计很快将建立更多的试验。这两个项目的主要目的都是改善从分子诊断到治疗的实施途径,以及诊断和肿瘤靶向治疗的报销,为欧洲的 PCM 提供最佳实践的范例。
PCM4EU 和 PRIME-ROSE 分别于 2023 年 1 月和 7 月启动。PCM4EU 网站(http://www.pcm4eu.eu)上已经提供了教育材料,包括一个播客系列。预计 2024 年将发布第一份报告,包括参与国家报销系统要求概述和患者参与指南。
PCM4EU 和 PRIME-ROSE 分别于 2023 年 1 月和 7 月启动。PCM4EU 网站(http://www.pcm4eu.eu)上已经提供了教育材料,包括一个播客系列。预计 2024 年将发布第一份报告,包括参与国家报销系统要求概述和患者参与指南。
欧洲合作可以促进 PCM 的实施,从而为更多患者提供负担得起和平等的精准诊断和匹配治疗。