Efficacy of HIPEC in the Treatment of Advanced-Stage Epithelial Ovarian Cancer After Cytoreductive Surgery

NCT03373058 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 310

Last updated 2019-11-06

No results posted yet for this study

Summary

This project is a multi-center, prospective, randomized controlled clinical observation the safety and efficacy of hyperthermic intraperitoneal chemotherapy in the treatment of advanced-stage epithelial ovarian cancer after cytoreductive surgery. Median recurrence-free survival is the primary end points of this project.

Conditions

Interventions

PROCEDURE

Hyperthermic Intraperitoneal Chemotherapy

HIPEC is performed as postoperative chemotherapy after cytoreductive surgery for advanced-stage epithelial ovarian cancer. The first HIPEC is conducted within 48h after cytoreductive surgery: Paclitaxel 175 mg/m\^2, 43°C, 90min. The second HIPEC is performed after 48 hours of the first HIPEC. The HIPEC regimens are Docetaxel 75 mg/m\^2 and cisplatin 75 mg/m\^2, respectively, 43°C, 90min.

PROCEDURE

cytoreductive surgery

Cytoreductive surgery (CRS) is performed when Faggoti value is less than 6 via laparoscopic exploration.

DRUG

adjuvant chemotherapy

Systemic chemotherapy regimens after HIPEC treatment are paclitaxel 175 mg/m\^2 IV\>3 hour+ carboplatin AUC = 5-6 IV\>1 hour, every 3 weeks for 2 cycles in experimental group. Systemic chemotherapy regimens after IDS are paclitaxel 175 mg/m\^2 IV\>3 hour+ carboplatin AUC = 5-6 IV\>1 hour, every 3 weeks for 3 cycles in control group.

Sponsors & Collaborators

  • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

    collaborator OTHER
  • Third Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • Henan Provincial People's Hospital

    collaborator OTHER
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • The Third Xiangya Hospital of Central South University

    collaborator OTHER
  • Peking University Cancer Hospital & Institute

    collaborator OTHER
  • Peking University People's Hospital

    collaborator OTHER
  • Cancer Hospital of Guizhou Province

    collaborator OTHER
  • Chinese PLA General Hospital

    collaborator OTHER
  • Hebei Medical University Fourth Hospital

    collaborator OTHER
  • The Second Hospital of Hebei Medical University

    collaborator OTHER
  • West China Second University Hospital

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • First Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • Henan Cancer Hospital

    collaborator OTHER_GOV
  • Tianjin Medical University Cancer Institute and Hospital

    collaborator OTHER
  • The Third Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • Wuhan University

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • Obstetrics & Gynecology Hospital of Fudan University

    collaborator OTHER
  • Southern Medical University, China

    collaborator OTHER
  • Fourth Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • Shandong Cancer Hospital and Institute

    collaborator OTHER
  • Beijing Obstetrics and Gynecology Hospital

    collaborator OTHER
  • Chongqing University Cancer Hospital

    collaborator OTHER
  • Xinqiao Hospital of Chongqing

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • First Affiliated Hospital of Chongqing Medical University

    collaborator OTHER
  • Affiliated Cancer Hospital of Shantou University Medical College

    collaborator OTHER
  • Affiliated Cancer Hospital & Institute of Guangzhou Medical University

    lead OTHER

Principal Investigators

  • Shuzhong Cui, M.D · Affiliated Cancer Hospital & Institute of Guangzhou Medical University

  • Zhongqiu Lin, M.D · Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-15
Primary Completion
2021-07-01
Completion
2023-07-01

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03373058 on ClinicalTrials.gov