About this trial
This study comprises 3 stages:
1. Collection of tumor and blood samples. 2. Creation of organoid models based on tumor samples. 3. Development of functional tests to predict clinical response to treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patient aged 18 years or more
Patient with histologically confirmed, localized endometrial cancer, candidate for surgical treatment.
A high-grade endometrioid histological type and/or
P53 mutation and/or
Disqualifiers
Other active cancer less than 6 months old (with the exception of treated basal cell carcinoma of the skin).
Patient deprived of liberty, under guardianship, or subject to a legal protection measure, or unable to express consent.
Trial population
Patient with localized endometrial cancer
Trial design
Cohort
Prospective
Treatments tested in this trial
tumour and blood samples
Other interventionTumour and blood samples
Treatment groups
Trial outcomes
Primary outcomes
Rate of establishment of exploitable tumor organoid lines
Rate of establishment of tumor organoid lines usable for predictive assays of response to PARP inhibitors.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.