French Assessment of MRD by Liquid Biopsies in Colorectal With Liver Metastasis Patients (FRENCH.MRD.CRLM)
Condition(s) studied
Investigational drug(s) / intervention(s)
Blood sample/Liquid biopsy: ctDNA analysis
Study summary
Improving personalized cancer treatments and finding the best strategies to treat each patient relies on using new diagnostic technologies. Currently, for colorectal cancer, the methods used to decide who gets additional post-surgery treatment are suboptimal. Some patients get too much treatment, while others do not get enough.
There is a new way to explore if there is any cancer left in a patient's body using circulating tumor DNA (ctDNA) detected in blood samples. This can help decide who needs more treatment after surgery. Even though many tests have been developed, it has yet to be determined which test performs best at relevant time points.
The GUIDE.MRD consortium is a group of experts, including scientists, technology, and pharmaceutical companies. The consortium is working on creating a reliable standard for the ctDNA tests, validating their clinical utility, and collecting data to help decide on the best treatment for each patient.
FRENCH.MRD.CRLM is the French study and part of the european GUIDE.MRD project.
Eligibility
Primary outcome measure(s)
- 3-year disease free survival — 3-year after the end of inclusion
Disease-free survival was defined as the time between the date of the baseline blood sampling/inclusion and the date of the first event among or recurrence or death from any cause.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU de Montpellier | Montpellier | France | Recruiting |
| Institu régional du Cancer de Montpellier (ICM) | Montpellier | France | Recruiting |
More University Hospital, Montpellier trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06287723 on ClinicalTrials.gov ↗ ← All trials in France