Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Institut de Cancérologie de Lorraine
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Age ≥ 18 years
Patient with stage III to IV non-treated high grade ovarian cancer or recurrent high grade ovarian cancer
Adequate haemoglobin rate ≥ 9 g/dL
Patient who can benefit from an additional blood sample of 20ml. The total volume of each sample meets with the indications of the Order in force establishing the list of researches mentioned in 2 ° of Article L. 1121-1 of the Public Health Code.
Availability of tumor samples from biopsy or surgery
Patient affiliated to a social security scheme
Ability to provide written informed consent
You may not be if
Any concurrent severe and/or uncontrolled medical conditions which could compromise participation in the study
Contraindication to a blood sample of 20 mL
Pregnant or breast-feeding women
Ongoing treatment for the newly diagnosed cancer or the recurrence
Patient pre-treated with poly-ADP-ribose-polymérase-1 (PARP) Inhibitors
Patient under guardianship or curatorship or deprived of liberty.
