Breast Cancer Clinical Trial
Prospective Breast Cancer Biospecimen Collection
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
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
Patient must be undergoing one of the following:
definitive surgical tumor resection for breast cancer OR
placement of a vascular access device as a prelude to neoadjuvant therapy for breast cancer OR
neurosurgical resection of a brain metastasis from primary breast cancer.
<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
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