Surgical Complications Related to Primary or Interval Debulking in Ovarian Neoplasm (SCORPION)
Stage IIIC Ovarian Cancer
About this trial
This is an interventional treatment trial for Stage IIIC Ovarian Cancer
Eligibility Criteria
Inclusion Criteria:
- Patients with suspected advanced ovarian cancer (FIGO stage IIIC)
- PIV ≥ 8, PIV ≤ 12
- Estimated life expectancy of at least 4 weeks.
- PS ≤ 2
- Appropriate respiratory, hepatic, cardiological, bone marrow and renal functions (Creatinine Clearance > 60 mL/min according to Cockcroft formula)
- Patient capable of consent.
Exclusion Criteria:
- Pregnancy or breastfeeding.
- Non-appropriate respiratory, hepatic, cardiological, bone marrow and renal functions
- Large size mass reaching the xiphoid, occupying all the abdominal cavity and/or infiltrating the abdominal wall.
- Mesenteric retraction
Sites / Locations
- Catholic University of the Sacred Heart
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Primary debulking surgery
Interval debulking surgery
All patients with suspicion of advanced ovarian carcinoma (FIGO stage IIIC) will undergo to a diagnostic laparoscopy in order to obtain a laparoscopic score (PIV) based on seven parameters: omental cake, peritoneal and diaphragmatic extensive carcinosis, mesenteric retraction, bowel and stomach infiltration, spleen and/or liver superficial metastasis, as previously published (Fagotti et al, American Journal of Obstetrics and Gynecology, 2008) Patients with PIV ≥ 8 and ≤ 12 randomized in this group will be submitted to an attempt of primary debulking surgery in order to obtain RT < 1 cm, followed by adjuvant chemotherapy.
All patients with suspicion of advanced ovarian carcinoma (FIGO stage IIIC) will undergo to a diagnostic laparoscopy in order to obtain a laparoscopic score (PIV) based on seven parameters: omental cake, peritoneal and diaphragmatic extensive carcinosis, mesenteric retraction, bowel and stomach infiltration, spleen and/or liver superficial metastasis, as previously published (Fagotti et al, American Journal of Obstetrics and Gynecology, 2008) Patients with PIV ≥ 8 and ≤ 12 randomized in this group will be submitted only to diagnostic laparoscopy followed by neoadjuvant chemotherapy and subsequent Interval Debulking Surgery, followed by further cycles of chemotherapy.