About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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.
Disqualifiers
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.
Trial population
Participants receiving screening mammograms at MD Anderson site
Trial design
Cohort
Prospective
Treatments tested in this trial
Biospecimen Collection
Procedure/SurgeryUndergo collection of blood samples
Mammography
Procedure/SurgeryUndergo standard of care mammography
Questionnaire Administration
Other interventionComplete questionnaires
Treatment groups
Trial outcomes
Primary outcomes
Creation of a repository of blood specimens and database of imaging, clinical data, health measurements, and questionnaire data
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
M.D. Anderson Cancer Center
Lead sponsor
National Cancer Institute (NCI)
Collaborator