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NCT Number: NCT05236686

Survival Effect of Hepato-celiac Lymphadenectomy In Primary or Relapsed Ovarian Cancer

The purpose of this study is to evaluate the safety and the effectiveness of hepato-celiac lymphadenectomy in the treatment of primarily diagnosed advanced epithelial ovarian cancer and platinum-sensitive recurrent ovarian cancer.

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Key information

About this study

This single-arm, multi-center, phase II trial is to evaluate the safety and effectiveness of hepato-celiac lymphadenectomy in the treatment of ovarian cancer with hepato-celiac lymph nodes metastases, in the circumstance of primarily diagnosed advanced epithelial ovarian cancer (primary debulking surgery or interval debulking surgery) and of platinum-sensitive recurrent ovarian cancer (no more than 4 lines of therapy).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18 years to ≤ 75 years.
  • Pathologic confirmed stage III or IV epithelial ovarian cancer, fallopian tube cancer or primary peritoneal carcinoma (EOC, PPC, FTC) or platinum sensitive, relapsed EOC, PPC or FTC (no more than 4 lines of therapy)
  • Hepato-celiac lymph nodes metastases diagnosed by imaging before surgery and enlarged palpable lymph nodes by surgical findings
  • Assessed by the experienced surgeons, complete resection is feasible according to preoperative evaluation
  • 1 to 3 episodes of neoadjuvant chemotherapy is allowed in primary settings
  • Platinum sensitive relapse is defined as those with platinum-free interval of 6 months or more.
  • ASA score of 1 to 2
  • ECOG performance status of 0 to 2
  • Adequate bone marrow, liver and renal function to receive chemotherapy and subsequently to undergo surgery:
  • White blood cells >3,000/µL, absolute neutrophil count ≥1,500/µL, platelets ≥100,000/µL, hemoglobin ≥9 g/dL,
  • Serum creatinine <1.25 x upper normal limit (UNL) or creatinine clearance ≥60 mL/min according to Cockcroft-Gault formula or to local lab measurement
  • Serum bilirubin <1.25 x UNL, AST(SGOT) and ALT(SGPT) <2.5 x UNL
  • Comply with the study protocol and follow-up.
  • Written informed consent.

Exclusion criteria

  • Patients with non-epithelial ovarian cancer, fallopian tube cancer or primary peritoneal carcinoma.
  • Low-grade carcinoma.
  • Mucinous ovarian cancer.
  • Infeasible complete resection according to preoperative evaluation
  • Unresectable pulmonary and hepatic parenchymal metastases, multiple thoracic lymph nodes metastases, brain or bone metastases according to preoperative evaluation.
  • Carcinomatosis on small bowel mesentery or intestinal wall by surgical findings and infeasible optimal surgery by bowel resection or peritonectomy.
  • Progression after neoadjuvant chemotherapy in primary settings.
  • Synchronous or metachronous (within 5 years) malignancy other than carcinoma in situ or breast cancer (without any signs of relapse or activity).
  • Any other concurrent medical conditions contraindicating surgery or chemotherapy that could compromise the adherence to the protocol.
  • Other conditions, such as religious, psychological and other factors, that could interfere with provision of informed consent, compliance to study procedures, or follow-up.

Treatment and study plan

Hepato-celiac lymphadenectomy

Procedure

Hepato-celiac lymphadenectomy in the treatment of epithelial ovarian cancer, with a maximum cytoreduction, in the circumstance of primarily diagnosed advanced epithelial ovarian cancer (primary debulking surgery or interval debulking surgery) and of platinum-sensitive recurrent ovarian cancer (no more than 4 lines of therapy).

Primary outcomes

  1. 2-years Non-Progression Rate

    Time frame: Participants will be followed up to 2 years after randomization

    The proportion of patients without disease progression or death at 2 years after entry into the study.

Secondary outcomes

  1. Progression free survival

    Time frame: Participants will be followed up to 24 months after randomization

    The time from entry into the study to the diagnosis of the first progression or recurrence or death, whichever occurs first

  2. Overall survival

    Time frame: Participants will be followed up to 60 months after randomization

    The time from date of randomization until the date of death from any cause or last follow-up

  3. Objective response rate

    Time frame: Participants will be followed up to 24 months after randomization

    The proportion of patients who achieved complete response (CR) or partial response (PR)

  4. Disease control rate

    Time frame: Participants will be followed up to 24 months after randomization

    The proportion of patients who achieved complete response (CR) or partial response (PR) or stable disease (SD)

  5. Post-operative complications

    Time frame: Participants will be followed up to 90 days after randomization

    Postoperative 30-day, 60-day and 90-day complications

  6. Quality of life assessments (QLQ-C30)

    Time frame: Baseline; 6 months, 12 months and 24 months after randomization

    Assessment of potential impact of first line treatment on functionality and well-being in patients by the EORTC core quality of life questionnaire (QLQ-C30, version 3.0).

  7. Quality of life assessments (FACT-Q)

    Time frame: Baseline; 6 months, 12 months and 24 months after randomization

    Assessment of potential impact of first line treatment on functionality and well-being in patients by functional assessment of cancer therapy-ovary (FACT-O, version 4).

  8. Patterns of subsequent recurrence

    Time frame: Participants will be followed up to 24 months after randomization

    The number and sites of subsequent recurrence, including pelvic, abdominal, retroperitoneal lymph nodes, hepato-celiac lymph nodes and distant metastases and ascites, etc.

Study contacts

Contact information is provided by the study sponsor or research team.

Libing Xiang

CONTACT

[email protected]

862164041990 ext. 2801

Rong Jiang

CONTACT

[email protected]

86 21 64041990 ext. 2801

Sponsors and collaborators

Lead sponsor

Shanghai Gynecologic Oncology Group

Other Gov

Collaborators

  • Fudan University

Registry information

Official study title

A Prospective, Multi-center, Single-Arm Phase II Clinical Study to Evaluate Safety and Effectiveness of Hepato-celiac Lymphadenectomy in the Treatment of Advanced and Recurrent Ovarian Cancer

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Feb 11, 2022
Registry last updated
Nov 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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