Trials / Active Not Recruiting
Active Not RecruitingNCT03672331
My Personalized Breast Screening
International Randomized Study Comparing Personalized, Risk-Stratified to Standard Breast Cancer Screening In Women Aged 40-70
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 53,142 (actual)
- Sponsor
- UNICANCER · Academic / Other
- Sex
- Female
- Age
- 40 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
MyPeBS is an international randomized, open-label, multicentric, study assessing the effectiveness of a risk-based breast cancer screening strategy (using clinical risk scores and polymorphisms) compared to standard screening (according to the current national guidelines in each participating country) in detecting stage 2 or higher breast cancers. Women will be differentially screened for 4 years and then, after an end-of-study mammogram, they will return to the routine screening practice. The main study endpoint will be measured at the end of the four years of intervention. Furthermore, follow up data will be collected for 15 years from study entry for evaluation of long-term cumulative breast cancer incidence and breast cancer-specific survival
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Mammogram | Every 1-4 years according to the national/regional guidelines or personalised schedule according to risk assessment |
| OTHER | Ultrasound | As required according to the national/regional guidelines or personalised schedule according to risk assessment |
| OTHER | MRI | As required according to the national/regional guidelines or personalised schedule according to risk assessment |
| OTHER | Tomosynthesis | As required according to the national/regional guidelines or personalised schedule according to risk assessment |
Timeline
- Start date
- 2019-07-18
- Primary completion
- 2027-08-31
- Completion
- 2027-12-31
- First posted
- 2018-09-14
- Last updated
- 2025-09-18
Locations
6 sites across 6 countries: Belgium, France, Israel, Italy, Spain, United Kingdom
Source: ClinicalTrials.gov record NCT03672331. Inclusion in this directory is not an endorsement.