Clinical Trials in France / NCT04938986
Recruiting
Not applicable
Interest of the Immunoscore® as a Post-operative Complementary Tool for the Detection of the Risk of Recurrence in Patients With Nonmetastatic Colorectal Cancer
NCT04938986 · tracked via the Priya Life Science France tracker
Condition(s) studied
Non Metastatic Colorectal Cancer
Investigational drug(s) / intervention(s)
IMMUNOSCORE®
IMMUNOSCORE®: recommendation for patient care according to the result of the IMMUNOSCORE®
Study summary
Evaluate the patient care recommandation induced by the IMMUNOSCORE® result
Eligibility
Inclusion Criteria:
* age between 18 and 80 inclusive;
* histologically confirmed colon adenocarcinoma;
* having undergone a curative resection of stage I, II or III colorectal cancer;
* diagnosed T1 / T2 / T3 / T4 and N0 / N1 / N2;
* eligible to receive 6 months of adjuvant chemotherapy;
* having given free, informed and written consent;
* agreeing to the use of a tumor sample for research purposes;
* being affiliated to a social security system.
Exclusion Criteria:
* pregnant or breastfeeding women
* legal incapacity or physical, psychological, social or geographical conditions preventing the patient from signing the consent or completing the study.
* history of other solid tumor within 3 years before inclusion, with the exception of in-situ cancer of the cervix and skin cancers (basal or squamous) treated and controlled
* person subject to a safeguard measure.
Primary outcome measure(s)
- Number of cases where the recommendations for patient care according to the Immunoscore® are considered beneficial compared to the standard care decision — 5 years
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Hôpital Européen | Marseille | France | Not Yet Recruiting |
| Hopital Saint Joseph | Marseille | France | Recruiting |
More Hospital St. Joseph, Marseille, France trials in France
Official registry record
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 NCT04938986 on ClinicalTrials.gov ↗ ← All trials in France