Breast Cancer Survivorship Biorepository

Description

This study collects blood samples as well as clinical and self-report data from stage I-III breast cancer survivors to create a biorepository for future use. The creation of this biorepository will allow for future research into links between individual, molecular, and genomic signatures and cancer outcomes.

Conditions

Anatomic Stage I Breast Cancer AJCC v8, Anatomic Stage II Breast Cancer AJCC v8, Anatomic Stage III Breast Cancer AJCC v8, Invasive Breast Carcinoma

Study Overview

Study Details

Study overview

This study collects blood samples as well as clinical and self-report data from stage I-III breast cancer survivors to create a biorepository for future use. The creation of this biorepository will allow for future research into links between individual, molecular, and genomic signatures and cancer outcomes.

A Comprehensive Breast Cancer Survivorship Biorepository

Breast Cancer Survivorship Biorepository

Condition
Anatomic Stage I Breast Cancer AJCC v8
Intervention / Treatment

-

Contacts and Locations

Los Angeles

USC / Norris Comprehensive Cancer Center, Los Angeles, California, United States, 90033

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Women of all racial and ethnic groups 18 years of age or older
  • * Women with a diagnosis of invasive breast cancer (stages I-III) within the past 7 years
  • * Women who have completed active treatment for breast cancer (surgery, chemotherapy, HER2-directed therapy and radiation)
  • * Prior participation on clinical trials is allowed
  • * Current receipt of interventional clinical trial participation
  • * Stage IV (metastatic) cancer
  • * Prior history of recurrence (except recurrence following ductal carcinoma in situ)
  • * Inability to give informed consent
  • * Unable to speak English, Spanish, Chinese, or Korean

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Southern California,

Bodour Salhia, PhD, PRINCIPAL_INVESTIGATOR, University of Southern California

Study Record Dates

2028-04-11