Projecting cancer incidence and deaths to 2030: the unexpected burden of thyroid, liver, and pancreas cancers in the United States.
Lola Rahib, Benjamin D Smith, Rhonda Aizenberg...
https://pubmed.ncbi.nlm.nih.gov/24840647Actively Recruiting
Led by Institut du Cancer de Montpellier - Val d'Aurelle · Updated on 2025-02-12
120
Participants Needed
1
Research Sites
260 weeks
Total Duration
Pancreatic adenocarcinoma (PA) is a solid cancer with a very poor prognosis, having an overall survival rate of less than 5% at five years across all stages. The number of cases and deaths from PA has been rising steadily for two decades, and without new treatments, it is expected to become one of the leading causes of cancer deaths by 2030. This research focuses on understanding the tumor and its microenvironment, which includes various cells and extracellular components that influence tumor growth and resistance to treatments. New technologies like CyTOF are being used to analyze the cellular makeup of tumors and explore ways to disrupt harmful interactions between tumor cells and their surroundings. The study involves collecting biological samples such as blood and tissue from patients with pancreatic adenocarcinoma before and during their treatments, including surgery and chemotherapy. These samples will be used to develop and characterize patient-derived tumor models and analyze the tumors' molecular and genetic features. This approach aims to support personalized medicine strategies and improve understanding of drug resistance and tumor biology. The study is monocentric and prospective, building a clinical and biological database over several years. Participants will provide consent and have their clinical data recorded alongside biological samples collected throughout their treatment journey. Researchers will monitor patient participation rates and gather detailed information to evaluate tumor characteristics and treatment responses. The study will continue for up to eight years, allowing long-term observation and data collection to support future translational research and development of new therapies.
CONDITIONS
Prospective Monocentric Clinical-biological Database
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 8 years
Participants have blood and tissue samples collected before and during treatment, alongside standardized clinical data being entered into a database.
Visits occur before surgery and during treatment as needed for sample collection
Total: 1 location
1
Institut Régional du Cancer de Montpellier
Montpellier, Occ, France, 34298
Actively Recruiting
A
Aurore MOUSSION
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Lola Rahib, Benjamin D Smith, Rhonda Aizenberg...
https://pubmed.ncbi.nlm.nih.gov/24840647Ignacio Garrido-Laguna, Manuel Hidalgo
https://pubmed.ncbi.nlm.nih.gov/25824606Elena Gabriela Chiorean, Andrew L Coveler
https://pubmed.ncbi.nlm.nih.gov/26185420Belen Rubio-Viqueira, Antonio Jimeno, George Cusatis...
https://pubmed.ncbi.nlm.nih.gov/16899615W Leconet, C Larbouret, T Chardès...
https://pubmed.ncbi.nlm.nih.gov/24240689Charline Ogier, Pierre-Emmanuel Colombo, Corinne Bousquet...
https://pubmed.ncbi.nlm.nih.gov/29935372