About this trial

Optimal Timing of Surgery combined with Maintenance Therapy in the Front-line Treatment of Advanced Ovarian Cancer

Eligibility criteria

Qualifiers

Females aged ≥ 18 years.

Pathologic confirmed stage IIIC and IV epithelial ovarian cancer, fallopian tube cancer or primary peritoneal carcinoma

Low, Middle tumor burden and high tumor burden with cPCI score ≤ 12 based on pre-operative CT or PET/CT examination

Complete cytoreduction can be achieved based on CT or PET/CT examination

Disqualifiers

Non-epithelial ovarian malignancies and borderline tumors

Low grade ovarian cancer

Mucinous ovarian cancer

Complete cytoreduction cannot be achieved according to preoperative evaluation, including pulmonary and hepatic parenchymal metastases, unresectable extensive pleural metastases, multiple thoracic lymph nodes metastases, brain or bone metastases

Trial design

Treatments tested in this trial

  • Primary debulking surgery
  • Neoadjuvant chemotherapy
  • PARP inhibitor
  • Bevacizumab

Treatment groups

220 Participants
are divided into 2 treatment groups

Locations

9
The First People's Hospital of Foshan Foshan China
Sun Yet-Sen University Cancer Center Guangzhou China
The First Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China
Zhejiang Cancer Hospital Hangzhou China

Sponsors and collaborators

Shanghai Gynecologic Oncology Group

Lead sponsor

Fudan University

Collaborator