Secondary Interval Cytoreductive Surgery in Platinum-sensitive Recurrent Epithelial Ovarian Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorThe University of Hong Kong

About this trial

About 80% of advanced ovarian cancer patients recurred in 2-3 years. Secondary cytoreduction benefits selected patients who have high chance of complete resection. Whether secondary interval surgery can be used at recurrence is not known.

Eligibility criteria

Qualifiers

Histologically diagnosed EOC, fallopian tube or primary peritoneal carcinoma

>= 3 cycles of platinum-based chemotherapy, with or without bevacizumab and / or PARPi, at primary setting

Platinum-free interval should be >=6 months from the last dose of platinum-based chemotherapy

Upfront SCR not feasible

Disqualifiers

Non-epithelial or borderline tumors are excluded

Patients who have with concurrent malignancy within five years (except for basal or squamous cell skin cancer, in-situ breast cancer, stage 1a grade 1-2 endometrioid endometrial carcinoma without lymphovascular invasion) are excluded.

Patients using more than one line of chemotherapy are excluded.

Patients who have platinum-resistant or refractory recurrence are excluded.

Trial design

Treatments tested in this trial

  • Carboplatin or cisplatin
  • Paclitaxel, gemcitabine or liposomal doxorubicin with or without bevacizumab or biosimilar
  • Bevacizumab or biosimilar
  • Cytoreductive surgery

Treatment groups

18 Participants
are divided into 1 treatment group

Sponsors and collaborators