A Multi-Modality Surveillance Program for Women at High Risk for Breast Cancer
Status: | Recruiting |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 21 - Any |
Updated: | 2/23/2019 |
Start Date: | February 18, 2019 |
End Date: | December 20, 2023 |
Contact: | Ilona Siljander |
Email: | isiljanda@uchicago.edu |
Phone: | 773-702-2781 |
Personalized Risk-based Prevention for Diverse Populations of High Risk Women
This study is aimed to establish a registry of women undergoing intensive surveillance for
the early detection of breast cancer in high-risk women.
the early detection of breast cancer in high-risk women.
Inclusion Criteria:
1. Known BRCA1 or BRCA2, TP53, PALB2 carrier. Women with pathogenic mutations in any
other cancer susceptibility genes are eligible only if they also have a high PRS.
2. With life time risk of 40% or higher, based on Polygenic Risk Score that integrates
genetic and non-genetic factors.
3. Without prior breast cancer.
4. Must be older than 21 years.
5. Willing to travel to University of Chicago Medical Center for imaging studies as well
as any necessary follow-up procedures.
6. Be able to give informed consent.
Exclusion Criteria
1. Active cancer at the time of enrollment.
2. Current pregnancy or plans for pregnancy within two years of enrollment.
3. Presence of a pacemaker or any other metallic foreign objects in their body that
interferes with an MRI.
4. Breast surgery within two weeks of study entry.
5. History of kidney disease or abnormal kidney function.
- Women can be taking hormone replacement therapy, tamoxifen, raloxifene, aromatase
inhibitors or participating in a chemoprevention trial.
We found this trial at
1
site
Chicago, Illinois 60637
Principal Investigator: Olufunmilayo Olopade, MD
Phone: 773-702-2781
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