posted on 2020-06-25, 05:20authored byMelbourne Academic Centre for Health (MACH)
Population cohort of women, unaffected and affected by breast cancer, to investigate aspects of breast cancer risk and other important women's health issues. Collection of epidemiological information, mammogram images, breast cancer pathology data. Participants donate DNA and archival breast tumours are collected. Annual registry linkage to confirm cancer diagnoses and mortality data.
Yes. Dataset is an open resource, with access dependent upon review by the lifepool Access Committee and appropriate HREC.
Number of people/participants
54,000
Data source
Clinical
Research
Data source details
Data is collected from participants via Health & Lifestyle questionnaire and also from relevant clinical databases where the participant is diagnosed with cancer. Data also collected from BreastScreen and Cancer Registry.