Breast Tumor Tissue Repository for Cancer Research
This study is creating a collection (repository) of breast tumor tissue samples from core biopsies. By collecting these samples, doctors hope to learn more about how breast cancer grows and responds to treatments. This information could help develop better therapies and tests to guide treatment decisions in the future. You may be able to join if you are 18 or older and have known or suspected breast cancer, or a metastatic solid tumor (cancer that has spread) that originated in the breast. The study aims to develop this tissue bank and a secure database of information about the samples, and to create an efficient way for researchers to use these de-identified (anonymized) samples for breast cancer studies. The current recruitment status is unclear.
- Study design
- This is an observational study, meaning it collects information without assigning specific treatments. It plans to enroll up to 400 participants.
- What's involved
- You would undergo core needle biopsies of breast cancer in the breast, regional lymph nodes, and distant metastases, if applicable. Clinical and blood specimens would also be gathered.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study aims to develop and maintain the repository and database for up to 10 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Core Biopsies for Establishing a Breast Tumor Tissue Repository
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Evanthia Roussos-Torres, M.D. · PRINCIPAL_INVESTIGATOR · University of Southern California
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Development of a baseline and serial breast cancer core biopsy repository within the USC/Norris Comprehensive Cancer Center Women's Cancer ProgramUp to 10 years
- Development and maintenance of a secure clinical database of relevant demographic, clinical, pathologic, and longitudinal outcome characteristics of the samples to be bankedUp to 10 years
- Development of an efficient process for the distribution of de-identified samples from the bank to researchers with IRB-approved protocols or exemptions for the study of breast cancer-related questionsUp to 10 years