Prognostic and Predictive Biomarkers in Ovarian Cancers
Condition(s) studied
Investigational drug(s) / intervention(s)
Study summary
The investigators therefore propose to conduct a biological study of prospectively collected patient tumour samples, ascites, blood and other residual samples (feces, urine, vaginal smear) throughout the disease course where markers (at diagnosis and their change with treatment) will be correlated to outcome in order to investigate how genetic diversity in OC prior to treatment and adaptation following treatment contribute to chemotherapy resistance. In addition freshly collected ascitic samples (and tumour samples) will be subjected to ex vivo DNA repair functional assays and isolated in primary culture (and established as xenografts) for target validation experiments.
Eligibility
Primary outcome measure(s)
- Progression Free Survival — Correlation of baseline biomarkers with PFS will occur at 12 months following last patient inclusion
up to 12 months
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Gustave Roussy | Villejuif | Val de Marne | Recruiting |
More Gustave Roussy, Cancer Campus, Grand Paris 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 NCT03010124 on ClinicalTrials.gov ↗ ← All trials in France