Press release: PRIME-ROSE is now approved by the European Commission
PRIME-ROSE, a European precision cancer medicine trial network and implementation initiative, receives 6 million EUR from EU Cancer Mission!
The PRIME-ROSE project builds on a bottom-up, clinician-initiated family of PCM clinical trials which have been particularly successful in bringing up inclusion rates to offer additional lines of treatment and in providing patient benefit.
We are very excited to be an active part of PRIME-ROSE and thus contributing to steps towards the vision to secure access to affordable Precision Cancer Medicine (PCM) that prolongs life at the best quality possible for all cancer patients.
To the press-release: 👉 Matrix News
RIME-ROSE: A community of DRUP-like clinical trials using “Living Lab principles” for the implementation of precision cancer medicine in Europe.
PRIME-ROSE - A European precision cancer medicine trial network and implementation initiative funded by the EU Cancer Mission
The European Commission on 24 April 2023 approved the project Precision Cancer Medicine Repurposing System Using Pragmatic Clinical Trials, PRIME-ROSE. The project will officially start 1 July 2023 and is funded by the European Commission Horizon Europe Mission on Cancer (grant no. 101104269) with 5.969 mill EUR. PRIME-ROSE will run for five years (2023 – 2028). The consortium consists of altogether 24 partners, including nine beneficiaries and fifteen associated partners. In addition, PRIME-ROSE is part of the Cancer Mission cluster of projects on Diagnosis and Treatment.
Sustainable and affordable precision cancer medicine across Europe
The PRIME-ROSE vision is access to affordable Precision Cancer Medicine (PCM) that prolongs life at the best quality possible for all cancer patients. PCM is an approach that depends on access to adequate molecular diagnostics and drugs to have impact and move towards implementation in the national healthcare systems. Today there is inequality in access to PCM between and within EU countries, and while the promise of PCM is clear, implementation remains a challenge. This in particular affects cancer patients with the poorest prognosis who have exhausted all lines of standard of care treatment, those with tumours carrying rare mutations and patients with carcinoma of unknown primary.
The PRIME-ROSE project builds on a bottom-up, clinician-initiated family of PCM clinical trials which have been particularly successful in bringing up inclusion rates to offer additional lines of treatment and in providing patient benefit. These trials share the pragmatic clinical trial design of the original Dutch DRUP trial, with broad inclusion criteria and a limited set of endpoints. However, the trials are still anchored into national context and are funded independently. The result is a distributed DRUP-like clinical trial network that addresses local priorities while collaborating internationally for scale and impact.
Work to be done in PRIME-ROSE moving PCM forward in Europe
The consortium will use these existing adaptive and pragmatic clinical trial platforms to answer key questions regarding clinical effectiveness, provide health-economic evaluations, and contribute to scientific progress across cancers. In particular, the cross-country collaboration provided by PRIME-ROSE will build capacity as well as enable cross-trial data aggregation and analysis, initiate shared cohorts across borders and provide health-economic evaluations. To ensure successful implementation, the consortium will work together with regulators, policymakers, payers, healthcare providers and patient advocacy groups to implement evidence-based PCM in routine practice and address inequalities in access.
Altogether, this Europe-wide precision cancer medicine deployment will address key scientific and methodological questions to accelerate broad and equitable access to new and effective cancer treatments. The ongoing effort is already leading to harmonization, standardization, and pragmatic consensus.
Pan-European precision cancer medicine community
The pan-European PRIME-ROSE project is led by Professor Kjetil Taskén, Head of Institute for Cancer Research at Oslo University Hospital Comprehensive Cancer Centre in Norway.
Taskén is excited about the possibilities this project will enable and comments: “On behalf of the Consortium, I can say that we really look forward to growing and developing the community of DRUP-like clinical trials, work on their impact and accelerate the implementation of precision cancer medicine across Europe. PRIME-ROSE is an ambitious project only made possible by the joint efforts of my colleagues from all our twenty-four partner institutions”.
PRIME-ROSE Consortium Partners:
Oslo University Hospital, Oslo, Norway
Leiden University Medical Center, Leiden, The Netherlands
Stockholm School of Economics, Stockholm, Sweden
Capital Region, Copenhagen, Denmark
Helsinki University Hospital, Helsinki, Finland
Centre Leon Berard, Lyon, France
IPOPORTO, Porto, Portugal
Region Uppsala, Uppsala, Sweden
The Swedish Institute for Health Economics, Lund, Sweden
Karolinska Institutet, Stockholm, Sweden
Region Skåne, Sweden
Heidelberg University Hospital, Heidelberg, Germany
Maria Sklodowska-Curie Institute ofOncology,Warsaw, Poland
University Hospital of Split (KBC Split), Split, Croatia
Tartu University Hospital, Tartu, Estonia
National Institute of Oncolocy, Budapest, Hungary
Vall D’Hebron Institute of Oncology, Barcelona, Spain
Center for Personalized CancerTreatment(CPCT, DRUP trial consortium), hosted by Radboud University Medical Center,Nijmegen, The Netherlands
National Cancer Institute, Vilnius, Lithuania
Cancer Research UK, London, UK
University of Manchester, Manchester, UK
Trinity College Dublin, Dublin, Ireland
Masaryk Memorial Cancer Institute (MOU), Brno, Czech Republic,
Center for Innovation in Medicine (CIM), Bucharest, Romania - coordinating a PCM network in the Balkan states of Romania, Bulgaria, Moldova, Montenegro and Macedonia
Overview of DRUP-like clincial trials:
Selected Literature: