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NCT07889843Recruiting

Folate Receptor Alpha (FRα) Expression and Heterogeneity in Epithelial Ovarian Cancer

Source: ClinicalTrials.gov · Last updated 22 Oct 2026

Brief summary (registry, in English)

This is a single-country, retrospective, observational biomarker study conducted in Greece to evaluate Folate Receptor Alpha (FRα) expression in patients with high-grade serous ovarian, fallopian tube, and primary peritoneal cancer at the time of diagnosis. Approximately 200 eligible female patients (≥18 years) diagnosed between 1 January 2001 and 30 July 2025 will be included from around 15 clinical sites affiliated with the Hellenic Cooperative Oncology Group. Historically collected Formalin-Fixed Paraffin-Embedded (FFPE) tissue samples stored in the Hellenic Cooperative Oncology Group biobank will be analyzed centrally using the Ventana FOLR1 RxDx assay to determine FRα expression. Only samples collected at initial diagnosis will be included; relapse samples will be excluded. The primary objective is to assess the prevalence of FRα-positive status, defined as ≥75% viable tumor cells with moderate (2+) and/or strong (3+) membrane staining. Secondary objectives include evaluation of intra-tumoral heterogeneity, concordance between primary and metastatic lesions, prevalence of lower FRα expression levels, and associations between FRα expression and clinical characteristics, BRCA/HRD status, progression-free survival (PFS), and overall survival (OS). All analyses will be descriptive, with additional exploratory statistical methods including chi-square tests, Cohen's kappa, correlation analyses, ANOVA, Kaplan-Meier survival analysis, and Cox proportional hazards models. Data will be retrospectively collected from the Hellenic Cooperative Oncology Group registry and medical records and entered into a secure REDCap eCRF system.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
21 Jul 2026
Start date
10 Jul 2026
Primary completion date
30 Dec 2026
Lead sponsor
Hellenic Cooperative Oncology Group
NCT number
NCT07889843

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 10 Jul 2026 to the primary completion date, 30 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Diagnosis of non-epithelial ovarian tumors
  • Diagnosis of endometrioid, mucinous, or clear cell carcinomas.
  • Inadequate (poor quality or inadequate posology for analysis) tissue samples.

Who the study is looking for

  • Female patients.
  • 18 years of age or older.
  • Patients diagnosed with high-grade serous epithelial ovarian cancer according to pathologists' report.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hellenic Cooperative Oncology Group
Coordinator of this site? Confirm its status
AthensGreeceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.