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NCT05236686

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

Recruiting · Not Applicable · Shanghai Gynecologic Oncology Group · registry updated 2025-11-19

Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.

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.

Inclusion

  • 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
  • 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.

Exclusion

  • 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.

Open NCT05236686 on ClinicalTrials.govAll conditions