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PCM4EU and PRIME-ROSE: Collaboration for implementation of precision cancer medicine in Europe

K. Taskén, S. F Haj Mohammad, GL. Fagereng, R. Sørum Falk, Å. Helland, S. Barjesteh van Waalwijk van Doorn-Khosrovani, K. Steen Carlsson, B. Ryll, K. Jalkanen, A. Edsjö, HG. Russnes, U. Lassen, E. Hallersjö Hult, I. Lugowska, JY. Blay, L....

. 2024 ; 63 (-) : 385-391. [pub] 20240523

Jazyk angličtina Země Švédsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc24013880

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

CZ Health Insurance Tilburg The Netherlands

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 Molecular Oncology and Immunology Netherlands Cancer Institute Amsterdam The Netherlands

Department of Oncology Institute of Clinical Sciences Sahlgrenska Academy at University of Gothenburg Gothenburg Sweden

Department of Oncology Rigshospitalet Copenhagen University Hospital Copenhagen Denmark

Department of Oncology Sahlgrenska University Hospital Gothenburg Sweden

Department of Pathology Oslo University Hospital Oslo Norway

Division of Cancer Medicine Oslo University Hospital Oslo Norway

Division of Cancer Sciences The University of Manchester and The Christie NHS Foundation Trust Manchester UK

Hematology Oncology Clinic at Tartu University Hospital Tartu Estonia

Institute for Cancer Research Oslo University Hospital and Institute of Clinical Medicine University of Oslo Oslo Norway

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

Citace poskytuje Crossref.org

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$a 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.
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