About this trial
Tissue will be procured during a standard of care procedure the patient will already be scheduled to undergo. A one time blood draw will be performed at this time and an optional rectal swab for biome analysis may occur. Follow Up will only consist of chart review to determine date of recurrence, metastases, and/or death
Eligibility criteria
Qualifiers
Adults >18 years old at time of consent
Subject must be capable to giving informed consent or have an acceptable surrogate capable of giving consent on the subject behalf.
Patients with carcinoma in situ or invasive breast cancer
definitive surgical tumor resection for breast cancer OR
Disqualifiers
<18 years old
Not able to give informed consent and does not have acceptable surrogate capable to giving informed consent.
Active drug/alcohol dependence or abuse history
Trial design
Treatments tested in this trial
- Tissue Sample collection
- Blood Sample Collection
- Rectal Swab
Treatment groups
Locations
1Sponsors and collaborators
Thomas Jefferson University
Lead sponsor