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The BCB is a tool:
The creation of a broad clinical and biological prospective base dedicated to different types of cancer is essential for the development of such projects.
Full description
Implementation of a translational research project is part of the Cancer Plan 2014-2019 and its axis 5 "Advancing clinical and translational research in oncology", and more precisely Action 5.1.
The national health strategy launched by the Minister of Health and the Minister of Research will allow a better integration between research, innovation, medicine and care for the benefit of patients and society.
Moreover, knowledge of mechanisms involved in the phenomena of tumor invasion, metastatic dissemination, resistance to treatment and companion testing is crucial for the emergence of new biomarkers and therapeutic innovation.
However, the study of the earliest phases of tumorigenesis as well as of the advanced stages of the disease are currently limited by the low availability of blood and tissue samples combined with quality and reliable clinical data.
To meet these demands, the research must then integrate databases creation open to researchers and the ongoing evaluation of the impact of projects on the health of cancer patients.
Integrated research associated with quality biological research is the guarantee of medical progress.
The multidisciplinary structure around collections of biological resources will enable the various actors to harmonize not only the collection but also the sharing of their data with a view to making them available for medico-scientific projects at a regional and national dimension. The Clinical Biological Database (BCB) should be used to identify and characterize new molecular markers for better diagnosis and / or treatment. It should also permit to optimize the collection of all this information, their integration and their transversal exploitation by different research disciplines (epidemiological, fundamental, translational, clinical).
The BCB is a tool:
The creation of a broad clinical and biological prospective base dedicated to different types of cancer is essential for the development of such projects
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Age> at 18 years old,
Patient with invasive or in situ tumor pathology (proven or suspected) any stage confounded,
Patient in ICM at diagnosis
Naïve patient of any treatment for the present cancer,
Patient requiring treatment involving at least one (or more) tumor surgery (s)
Patient who has accepted supplementary blood samples,
Patient having given his informed, written and express consent.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
2,850 participants in 1 patient group
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Central trial contact
david azria
Data sourced from clinicaltrials.gov
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