Interval Cytoreductive Surgery With or Without HIPEC for Ovarian Cancer (FOCUS / KOV-HIPEC-04)

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-80
SponsorNational Cancer Center, Korea

About this trial

Primary stage III-IV epithelial ovarian cancer randomizing between interval cytoreductive surgery with or without hyperthermic intraperitoneal chemotherapy (HIPEC)

Eligibility criteria

Qualifiers

Signed and written informed consent,

Patients ≥18, <80 years old,

Diagnosed with histologically confirmed FIGO stage III-IV primary epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer treated with three cycles of neoadjuvant chemotherapy,

Treated with interval complete cytoreduction, or cytoreduction with no more than 2.5 mm depth of residual disease,

Disqualifiers

Diagnosed with non-epithelial ovarian carcinoma or borderline ovarian tumor

Patients who have not undergone neoadjuvant chemotherapy,

Interval cytoreduction with more than 2.5 mm depth of residual disease,

A life expectancy ≤3 months as clinically judged,

Trial design

Treatments tested in this trial

  • Cisplatin

Treatment groups

520 Participants
are divided into 2 treatment groups

Sponsors and collaborators