OV Precision: Study Examining the Benefit of a Tumor- and Patient-specific Cancer Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorSwiss GO Trial Group

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

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Swiss GO Trial Group

Lead sponsor

Tumor Profiler Center Switzerland

Collaborator