Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

Genetic risk prediction for hereditary ovarian cancer

Official title: A Cohort Study of Hereditary Ovarian Cancer Risk Prediction Models and Pathogenesis Exploration

Run by Peking University Third Hospital · NCT06564428 · Data updated 2026-11-12

This study is trying to create a way to predict the risk of ovarian cancer in families with a history of the disease to help guide prevention efforts for those at high risk.

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment1000 (estimated)
SponsorPeking University Third Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedJanuary 1, 2024
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedJune 18, 2025
Trial IDNCT06564428 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals diagnosed with epithelial ovarian cancer who have germ line pathogenic or suspected pathogenic mutations.

Probably not a fit

Patients with non-epithelial ovarian cancer or those who have not undergone genetic testing may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to establish a multicenter cohort of hereditary ovarian cancer patients in China to analyze their clinicopathologic features and develop a risk prediction model. By following up on clinical and pathological data, genetic test results, and family histories, the study seeks to quantify cancer risk in first-degree relatives of mutation carriers. Additionally, it aims to identify novel tumor-causing mutations and predisposing genes through gene sequencing in families with hereditary tumors. The ultimate goal is to guide preventive interventions for high-risk populations.

Why it matters

Potential benefit: If successful, this study could significantly improve risk assessment and management strategies for individuals at high risk of hereditary ovarian cancer.

How similar studies have gone: Other studies have shown success in developing genetic risk prediction models for various cancers, suggesting potential for this approach in ovarian cancer as well.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Epithelial ovarian cancer
* ≥18 years
* The pathological diagnosis was clear
* The genetic test showed germ line pathogenic/suspected pathogenic mutations (for mutation interpretation, refer to the American ACMG Classification Standards and Guidelines for Genetic Variation)

Exclusion Criteria:

* Non-epithelial ovarian cancer was confirmed by pathology
* No genetic test has been performed

Where it's running

  • Peking University Third Hospital
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

  • Principal investigator: Hongyan Guo, Doctor — Peking University Third Hospital
  • Study coordinator: Yuan Li, Doctor
  • Email: yuanli@bimu.edu.cn
  • Phone: 18610689868

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.