The Fred & Pamela Buffett Cancer Center

Patient Care
- Research Overview
- - Membership Directory
    Search a listing of full members of the Fred & Pamela Buffett Cancer Center, as well as directories of members by research program.
  - Membership Criteria
    Learn about the criteria for becoming a member of the Fred & Pamela Buffett Cancer Center.
  - Become a Member
    Apply for membership in the Fred & Pamela Buffett Cancer Center by submitting a short form.
- - Shared Resources
    The Fred & Pamela Buffett Cancer Center is home to state-of-the-art facilities and provides support to shared resources at UNMC.
  - UNMC Cores and Shared Resources
    Researchers also have access to shared resources through the UNMC Office of the Vice Chancellor for Research.
  - Request Research Space
    Complete this form to request research space.
- - Cancer Biology Program
    The Fred & Pamela Buffett Cancer Center Cancer Biology Program represents a long-standing commitment to cancer mechanisms-focused research.
  - Targets, Modulators and Delivery Program
    This program develops and delivers small molecules to modulate validated cancer targets as eventual cancer therapeutics.
  - Cancer Prevention & Control Program
    This program aims at identifying and understanding the factors influencing cancer risk, with a special emphasis on disparities and rural populations in the catchment area.
- - Registries
    View registries that are currently enrolling subjects through iCaRe2.
  - Information for Patients
    Participation helps researchers understand specific cancer types, determine risk factors, advance treatment for patients and discover cancer prognostic markers.
  - Information for Researchers
    iCaRe2 aims to foster clinical and epidemiological studies and accelerate the secondary use of cancer and health related data for translational research.
  - Information for Sponsors
    Your gift will support the continuous system growth and improve strides in personalized medicine, diagnosis, treatment and prevention of cancer.
- Community Outreach Overview
- Mission
  The Community Outreach and Engagement Office aims to reduce overall cancer burden and eliminate cancer-related health disparities in its catchment area.
- Community Advisory Board
  This board advises on the direction of cancer center research, dissemination of evidence from ongoing research activities, and policy recommendations.
- Speaker's Bureau
  The Fred & Pamela Buffett Cancer Center Speakers Bureau provides resources to community groups across Nebraska including experts to give presentations on cancer-related topics.
- Resources
  The Community Outreach and Engagement Office provides such resources as videos, infographics, reports and community needs assessments.
- Our Team
  Find members of the Community Outreach and Engagement Office team.
- Nebraska Breast Health Navigation Program
  This program is working to eliminate barriers for breast cancer survivors, using trained volunteers called Lay Patient Navigators who provide peer-to-peer support.
- Training & Education Overview
- Upper Midwest Emerging Scholars Exchange Program
  Learn about a new opportunity for Early Stage Investigators to share their research at peer institutions.
- Leadership Overview
- Director's Message
  Read a message from Joann Sweasy, PhD, director of the Fred & Pamela Buffett Cancer Center.
- About the Center
  Learn about the mission and vision of the Fred & Pamela Buffett Cancer Center.

— The Fred & Pamela Buffett Cancer Center — Research — Integrated Cancer Repository for Cancer Research — Registries — Breast Cancer Collaborative Registry

Breast Cancer Collaborative Registry

The Breast Cancer Collaborative Registry is a web-based system developed by the Fred & Pamela Buffett Cancer Center at the University of Nebraska Medical Center and operating under the umbrella of the integrated Cancer Data Repository for Cancer Research.

The registry is designed to provide collaborative platform to centers with expertise in breast cancer epidemiology, genetics, biology, early detection and patient care with the goal to facilitate rapid and uniform collection of critical information and biological samples to be used in developing prevention and treatment strategies against breast cancer.

The purpose of this project is to develop a national breast cancer resource, which collects demographic and lifestyle information, medical and family details, dietary and environmental exposure history as well as biospecimens from breast cancer patients, women at increased risk for breast cancer, and their family members.

The registry is available to all institutions interested in studies of risk factors influencing breast cancer development, progression and treatment or the effect of the disease and different treatments on the quality of life of breast cancer survivors. Institutional IRB approval and patient informed consent must be obtained.

The registry is committed to protecting each individual’s confidentiality/privacy online. Security issues are addressed using recommendations of the Healthcare Information and Management Systems Society Privacy & Security Toolkit and the electronic information security standards regarding the collection, use, and retention of data mandated by the Federal Health Insurance Portability and Accountability Act (HIPAA).