About this trial
The long-term goal of this research project is to demonstrate whether HRD negative (HPDneg) patients benefit when additional multi-modal biological tumor information is incorporated into the molecular tumor board (mTB) treatment recommendation process.
Eligibility criteria
Qualifiers
Newly diagnosed EOC (adenocarcinoma of the ovary, peritoneum, and fallopian tube) and carcinosarcoma patients with a suspected FIGO Stage III and IV
No immediate need of systemic or surgical treatment at time of and until 2 weeks after diagnosis
Envisaged surgical candidate for interval debulking after 2 cycles of treatment
Willing and able to attend the visits, to understand the purpose of the trial and all trial-related procedures
Disqualifiers
Elevated liver enzymes (double of normal range: ASAT > 68 U/l; ALAT > 82 U/l; GGT > 80 U/l)
Elevated creatinine (double of normal range: >120 mmol/l))
ECOG ≥3
Pregnant or lactating women
Trial design
Treatments tested in this trial
- Treatment recommendation by molecular tumorboard (mTB) based on tumor profiling
- Carboplatin / Paclitaxel Chemotherapy
Treatment groups
Sponsors and collaborators
Swiss GO Trial Group
Lead sponsor
Tumor Profiler Center Switzerland
Collaborator