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A Study to Collect Patients, Medical, and Biological Data From Patients Being Treated for Metastatic Colorectal Cancer With a Specific Genetic Mutation: BRAFV600E
The study will be conducted in patients with metastatic colorectal cancer (mCRC) harboring a BRAFV600E mutation, to collect clinical data and biological samples to be used for research but also to gather real-world clinical data concerning the treatments and the survival outcomes in patients with this pathology.
Despite substantial progress made in the first- and second line mCRC settings, there are still unmet clinical needs for patients harboring BRAFV600E mutations, especially those with microsatellite stability (MSS) / proficient mismatch repair (pMMR) tumor. The overall survival and access to different treatment in the real-life setting are unknown. Moreover, patient prognosis remains poor and therapeutic resistance to combinations with BRAF inhibitors, is at present, nearly universal. Therefore, it seems essential to prospectively collect clinical and biological data about this rare mCRC subtype. These data will allow us to improve knowledge and to identify clinical and biological factors that could drive therapeutic decisions, predict resistance to treatments, and that are prognostic for survival. In this context, we designed this large, prospective, cohort study to collect clinical data and biological samples to be used for research but also to gather real-world clinical data concerning the treatments and the survival outcomes in patients with BRAFV600E mCRC. This collection of clinical and biological data (tumor tissue and blood samples) will allow us to identify predictive and prognostic biomarkers with several research work packages planned: i. To evaluate the circulating tumor DNA (ctDNA) during the metastatic first-, second-, and third-line treatment to: * Evaluate its positive and negative predictive value. * Identify molecular alterations preceding and explaining clinical resistance during BRAF/EGFR inhibition therapy and immunotherapy. ii. To evaluate BRAFV600E mCRC immune environment both at the tumor and blood level (immunomonitoring). iii. To study specific the dMMR/MSI BRAFV600E subgroup. Furthermore, the data collected will describe the therapeutic management of BRAFV600E mCRC patients in the routine-practice setting which will bring very useful data. The results of the COBRAF study could lay the groundwork to better understand BRAFV600E mCRC and to identify prognostic and predictive biomarkers helping the development of new therapeutic approaches in this population.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Centre Hospitalier D'Avignon
Avignon, France
Centre Hospitalier de Bayeux
Bayeux, France
Chu Simone Veil
Beauvais, France
Institut Bergonie
Bordeaux, France
CH Fleyriat
Bourg-en-Bresse, France
Ch de Cahors
Cahors, France
CH Dr TECHER
Calais, France
Infirmerie Protestante de Lyon
Caluire-et-Cuire, France
Chu Estaing de Clermont-Ferrand
Clermont-Ferrand, France
GHPSO
Creil, France
Start Date
July 24, 2023
Primary Completion Date
July 1, 2027
Completion Date
July 1, 2028
Last Updated
December 10, 2025
400
ESTIMATED participants
Collection of blood samples
OTHER
Lead Sponsor
UNICANCER
Collaborators
NCT06625775
NCT04657068
Data Source & Attribution
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