BCCR Project

The Breast Cancer Collaborative Registry (BCCR) is aimed at gathering the BC-related information. The BCCR is designed to help with the standardization of data collection and reporting, and establish an infrastructure where by pooling efforts, resources and studies involving prevention and treatment strategies against BC can be furthered. The majority of the data is to be obtained from and submitted by the subject.

BCCR core data:

  • Date of birth
  • Date of study
  • Age at diagnosis/ age at study
  • Birth country
  • Gender
  • Marital status
  • Race/ethnic/heritage
  • Current Ht. & Wt.
  • Maximum Wt. ever
  • Education – highest level completed
  • Tobacco/smoking
  • Alcohol – current & past
  • Environmental exposures
  • Gynecologic History
  • Medical History
  • Dietary Habits
  • Imaging studies done
  • Stage (pathologic & clinical) at diagnosis
  • Medications
  • Other Medical Conditions
  • Any previous surgery
  • Ever involved in other breast cancer research
  • Summary of family history
  • Quality of Life Survey
  • Sleep Survey

 
 
BCCR Project
About Project
Security
Collaborative Registry
Participating Personnel
 
   
  Developed by and hosted at the University of Nebraska Medical Center
Fred & Pamela Buffett Cancer Center