- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06710015
Study on Fertility Parameters in Women With Germline Variants in BRCA1 and BRCA2 (BFert)
B.Fert: Retrospective and Prospective Observational Study on Fertility Parameters in Women With Germline Variants in BRCA1 and BRCA2
Pathogenic variants (PVs) in the BRCA1 and BRCA2 genes are associated with an increased risk of developing breast and ovarian cancers. According to current guidelines from the National Comprehensive Cancer Network, the risk of developing breast cancer exceeds 60% for both genes, while the risk for ovarian cancer ranges from 39% to 58% for the BRCA1 and from 13% to 29% for the BRCA2. The detection of a pathogenic variant in the BRCA1 or BRCA2 genes necessitates both the establishment of appropriate primary and secondary surveillance measures for carriers and the discussion of the familial implications of such findings.
The molecular basis initially suggesting a possible association between germline variants in BRCA1 and BRCA2 genes and diminished ovarian reserve lies in the cellular impact of impaired or defective repair of DNA double-strand breaks (DSBs) on oocytes. Notably, BRCA1 and BRCA2 genes play a key role in the ATM-related mechanism for DSB repair through the homologous recombination (HR) pathway.
Although preclinical evidence supports a potential correlation between defective DSB repair and normal follicle maturation processes, clinical studies on large cohorts of patients with pathogenic BRCA1 and BRCA2 variants yield inconsistent results. This discrepancy is likely attributable to the inherent challenges in recruiting a sufficiently homogeneous and statistically significant sample size.
The aim of the study is to evaluate reproductive capacity in women carrying pathogenic variants in the BRCA1/2 genes by assessing the number of pregnancies during the period from January 1, 2018, to December 31, 2023. Secondary objectives include evaluating menopausal characteristics and pregnancy outcomes.
Study Overview
Status
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Emanuela Lucci Cordisco, MD
- Phone Number: +39 0630156780
- Email: emanuela.luccicordisco@policlinicogemelli.it
Study Locations
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RM
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Roma, RM, Italy, 00136
- UOC Genetica Medica Fondazione Policlinico Universitario A.Gemelli IRCCS
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
BRCA1 and BRCA2 carriers
Inclusion Criteria:
- age > 18 years
- presence of a pathogenic variant in the BRCA genes
- signed informed consent Exclusion Criteria
- presence of a pathogenic variant in another gene (not BRCA)
- significant psychiatric or clinical impairment affecting the ability to consent to the study
Control cohort
Inclusion Criteria:
- Relatives up to the third degree of the first cohort who tested negative on predictive testing for the familial pathogenic variant in the BRCA genes, matched for age where possible.
Exclusion Criteria:
- absence of a pathogenic variant in another gene (non-BRCA) found in a family member
- significant psychiatric or clinical impairment affecting the ability to consent to the study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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BRCA1 and BRCA2 carriers
Inclusion criteria:
|
|
Control cohort
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluate the reproductive capacity in women carrying PVs in BRCA1/2 genes
Time Frame: 1 year
|
Evaluate number of pregnancies
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1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The evaluation of menopausal characteristics and pregnancy outcomes
Time Frame: 1 year
|
Evaluate: age at menopause, type of menopause, number of miscarriages, age at pregnancies, cancer diagnosis
|
1 year
|
Collaborators and Investigators
Investigators
- Principal Investigator: Emanuela Lucci Cordisco, Fondazione Policlinico Universitario A. Gemelli, IRCCS
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 6591 (CTEP)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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