An international worldwide retrospective cohort observational study comparing primary cytoreductive surgery with neoadjuvant chemotherapy and interval cytoreductive surgery in patients with carcinoma of the ovary, fallopian tubes, and peritoneum (SUROVA trial)

Int J Gynecol Cancer. 2024 Jun 3;34(6):942-945. doi: 10.1136/ijgc-2024-005354.

Abstract

Background: Currently, a lively debate exists within the scientific community regarding the most suitable procedure for treating stages IIIB-IVB carcinoma of the ovary, fallopian tubes, and peritoneum. The options under most consideration are primary cytoreductive surgery or neoadjuvant chemotherapy followed by interval cytoreductive surgery.

Primary objective: To compare overall survival at 5 years in patients who underwent primary cytoreductive surgery versus neoadjuvant chemotherapy and interval cytoreductive surgery for stage IIIB-IVB ovarian cancer STUDY HYPOTHESIS: The treatment with primary cytoreductive surgery results in superior patient survival compared with neoadjuvant chemotherapy followed by interval cytoreductive surgery.

Trial design: This is a multicenter, retrospective cohort observational study. Data will be collected from patients undergoing surgery in hospitals worldwide. Two arms will be compared: primary cytoreductive surgery and neoadjuvant chemotherapy followed by interval cytoreductive surgery.

Major inclusion/exclusion criteria: Patients must have suspected or histologically confirmed International Federation of Gynecology and Obstetrics (FIGO) stages IIIB-IVB ovarian, peritoneal, or fallopian tube cancers. They must have undergone primary surgery or first course of neoadjuvant chemotherapy between January 1, 2018 and December 31, 2019. Based on all available information before the surgery (primary or interval), the patient must have been considered completely resectable.

Primary endpoint: Overall survival at 5 years from the first treatment (chemotherapy in the case of neoadjuvant chemotherapy and cytoreduction in the case of primary cytoreductive surgery).

Sample size: An estimated total of 5000 patients will be enrolled in the study.

Estimated dates for completing accrual and presenting results: March 2025 TRIAL REGISTRATION: NCT06223763.

Keywords: Carcinoma, Ovarian Epithelial; Cytoreduction surgical procedures; Ovarian Cancer; Surgery; Surgical Oncology.

Publication types

  • Observational Study
  • Multicenter Study
  • Comparative Study

MeSH terms

  • Chemotherapy, Adjuvant
  • Cohort Studies
  • Cytoreduction Surgical Procedures* / methods
  • Fallopian Tube Neoplasms* / drug therapy
  • Fallopian Tube Neoplasms* / pathology
  • Fallopian Tube Neoplasms* / surgery
  • Female
  • Humans
  • Neoadjuvant Therapy*
  • Ovarian Neoplasms* / drug therapy
  • Ovarian Neoplasms* / pathology
  • Ovarian Neoplasms* / surgery
  • Ovarian Neoplasms* / therapy
  • Peritoneal Neoplasms* / drug therapy
  • Peritoneal Neoplasms* / mortality
  • Peritoneal Neoplasms* / pathology
  • Peritoneal Neoplasms* / surgery
  • Peritoneal Neoplasms* / therapy
  • Retrospective Studies

Associated data

  • ClinicalTrials.gov/NCT06223763