PRIMARY OBJECTIVES:
I. Determine the sensitivity of LBx for the presence of breast cancer in patient cohorts II. Determine the specificity of LBx for the presence of breast cancer in all patient cohorts.
OUTLINE: This is an observational study.
Patients undergo blood sample collection and have their medical records reviewed on study.
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
\* Women
* Age ≥ 18 years.
* Screening Mammography Cohort: Patients who were referred for screening mammography and had mammography performed within 6 months prior to blood draw or will be undergoing mammography within 6 months after blood draw. Patient must not have personal history of breast cancer, history of breast biopsy or prior abnormal mammography findings are allowed. OR
You may not be if
* New Beast Cancer Cohort: Patients with new biopsy proven diagnosis of breast cancer (invasive breast cancer or DCIS) within 60 days of blood draw who has not started any cancer directed therapy, including surgery, radiation, hormonal therapy or chemotherapy. Any breast cancer type patients at any stage are eligible. OR
* Remission Breast Cancer Cohort: Patients with personal history of localized breast cancer (stage 1, 2, 3) that has been previously treated with cancer directed therapy, such as surgery, chemotherapy, radiation and/or hormonal therapy who has been in completed remission. Patients must complete their surgery, adjuvant chemotherapy and/or radiation therapy prior to enrollment. The blood draw must occur at least 90 days after completion of the specified treatment modalities. Patients on adjuvant hormonal therapy are eligible to enroll (those who are treated with adjuvant hormonal therapy in combination with CDK4/6 inhibitor must complete CDK4/6 inhibitor therapy prior to enrollment).
\* Patients unable to give informed consent
* Patients who have received blood transfusion with 14 days prior to study blood draw
* Patients who had a heart attack, stroke, or pulmonary embolism within 3 months to study blood draw
* Excisional breast biopsy in the prior 30 days. Needle biopsy of the breast is permitted
