NCT lookup

Pull any trial record directly from ClinicalTrials.gov.

Implementing Polygenic Risk Scores for Breast Cancer Prevention: a Feasibility Study
Implementing Polygenic Risk Scores for Breast Cancer Prevention: a Feasibility Study

NCT06922708

RecruitingNA

Sponsor: Catholic University of the Sacred Heart

Conditions: Breast Cancer

Interventions: Clinical pathway for breast cancer prevention based on PRS-integrated CanRisk assessment

Countries: Italy

This single-arm interventional feasibility study will evaluate whether integrating polygenic risk scores (PRS) into the CanRisk model can improve breast cancer risk prediction and personalized prevention in women at risk of breast cancer. The study will assess the organizational feasibility, patient acceptance, emotional impact and satisfaction of an integrated pathway combining PRS testing with standard genetic counseling and other risk factors at Fondazione Policlinico Universitario Agostino Gemelli IRCCS.

Eligibility overview

Sex: FEMALE

Age: 18 Years to 79 Years

Healthy volunteers: Yes

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Ability to provide informed consent
* Voluntary consent to participate
* Estimated risk of carrying an inherited pathogenic variant (in BRCA1, BRCA2, PALB2, CHEK2, ATM, RAD51D, RAD51C, BARD1) \> 5%, (calculated on www.canrisk.org)
* Healthy women with:

  1. Known family history of breast cancer, or
  2. Known familiarity with carriers of pathogenic variants for genes included in the CanRisk model (BRCA1, BRCA2, PALB2, CHEK2, ATM, RAD51D, RAD51C, BARD1), or
  3. Known carriers of pathogenic variants for genes included in the CanRisk model (BRCA1, BRCA2, PALB2, CHEK2, ATM, RAD51D, RAD51C, BARD1)
* Affected women with:

  1. Diagnosis of unilateral breast cancer
  2. Personal history of ovarian cancer

Exclusion Criteria:

* Diagnosis or history of bilateral breast cancer
* Diagnosis of ductal carcinoma in situ
* Previous bilateral mastectomy
* Life expectancy \< 12 months due to other medical conditions
* Participation in interventional clinical trials for breast cancer prevention in the last 12 months
* Carriers or relatives of carriers of pathogenic variants in genes not included in the CanRisk model (genes other than BRCA1, BRCA2, PALB2, CHEK2, ATM, RAD51D, RAD51C, BARD1)
* Inability to provide informed consent
Locations (1)
  • Roma, Italy