Prognostic and Predictive Biomarkers in Ovarian Cancers

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• New patient with a diagnosis of OC, or

• Previously treated patient with frozen or formalin fixed paraffin embedded primary tumour sample available that can be retrieved by the center presenting with progressive disease, and consenting to CT guided biopsy of relapsed disease, or

• Previously treated patient with frozen or formalin fixed paraffin embedded primary tumour sample available that can be retrieved by the center scheduled for surgery for relapsed disease.

• Signed informed consent

• Age ≥ 18

• Patient affiliated to a social security regimen or beneficiary of the same

Locations
Other Locations
France
Gustave Roussy
RECRUITING
Villejuif
Contact Information
Primary
Alexandra LEARY, MD
alexandra.leary@gustaveroussy.fr
+33 (0)1 42 11 43 89
Backup
Damien DRUBAY
damien.drubay@gustaveroussy.fr
+33 (0)1 42 11 42 11
Time Frame
Start Date: 2016-09-26
Estimated Completion Date: 2032-09
Participants
Target number of participants: 350
Treatments
Other: Patients with ovarian cancer
Related Therapeutic Areas
Sponsors
Leads: Gustave Roussy, Cancer Campus, Grand Paris

This content was sourced from clinicaltrials.gov