PCM4EU and PRIME-ROSE: Collaboration for implementation of precision cancer medicine in Europe
Language English Country Sweden Media electronic
Document type Journal Article
PubMed
38779910
PubMed Central
PMC11332530
DOI
10.2340/1651-226x.2024.34791
Knihovny.cz E-resources
- MeSH
- European Union MeSH
- Precision Medicine * methods MeSH
- Clinical Trials as Topic organization & administration MeSH
- Humans MeSH
- Neoplasms * therapy MeSH
- Drug Repositioning MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Europe MeSH
BACKGROUND: 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. PATIENTS AND METHODS: 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. RESULTS: 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. CONCLUSION: 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. CONCLUSION: European collaboration can facilitate the implementation of PCM and thereby provide affordable and equitable access to precision diagnostics and matched therapies for more patients.
Centre Léon Bérard Lyon France
Clinical Trial Unit Comprehensive Cancer Centre Helsinki University Hospital Helsinki Finland
Department of Clinical Genetics Pathology and Molecular Diagnostics Region Skåne Malmö Sweden
Department of Medical Oncology Erasmus MC Cancer Institute Rotterdam The Netherlands
Department of Medical Oncology Leiden University Medical Centre Leiden The Netherlands
Department of Oncology Rigshospitalet Copenhagen University Hospital Copenhagen Denmark
Hematology Oncology Clinic at Tartu University Hospital Tartu Estonia
Instituto Português de Oncologia do Porto FG Porto Portugal
Maria Sklodowska Curie Institute of Oncology Warsaw Poland
Oslo Centre for Biostatistics and Epidemiology Oslo University Hospital Oslo Norway
Stockholm School of Economics Institute for Research Stockholm Sweden
Swedish Institute for Health Economics Lund Sweden
Trinity St James Cancer Institute Trinity College Dublin Ireland
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