This study collects mammogram images, blood samples, and clinical information from women undergoing routine screening mammograms. Creating a bank of blood samples and a database of clinical and risk information may be used in future research related to breast cancer, other cancers, and women's health.
Willingness to participate in the study and ability to provide informed consent
Willingness to complete a questionnaire and to provide a blood sample at the initial visit and at follow up annual visits
Undergoing a screening mammogram at participating sites. Subjects undergoing routine annual diagnostic mammograms or CEM as part of a screening study are also eligible.
Current or recent (within the prior 6 months) history of breast feeding
Personal history of breast cancer (ductal breast carcinoma in situ [DCIS] or invasive breast cancer)
Personal history of any other cancer (excluding in-situ, stage 0, and non-melanoma skin cancers and other pre-cancerous conditions) treated within the last 5 years.
M.D. Anderson Cancer Center
Lead sponsor
National Cancer Institute (NCI)
Collaborator