Prospective Breast Cancer Biospecimen Collection

Description

Tissue will be procured during a standard of care procedure the patient will already be scheduled to undergo. A one time blood draw will be performed at this time and an optional rectal swab for biome analysis may occur. Follow Up will only consist of chart review to determine date of recurrence, metastases, and/or death

Conditions

Breast Cancer, Invasive Breast Cancer, Carcinoma in Situ of the Breast

Talk to us

Study Overview

On this page

Study Details

Study overview

Tissue will be procured during a standard of care procedure the patient will already be scheduled to undergo. A one time blood draw will be performed at this time and an optional rectal swab for biome analysis may occur. Follow Up will only consist of chart review to determine date of recurrence, metastases, and/or death

Prospective Breast Cancer Biospecimen Collection

Prospective Breast Cancer Biospecimen Collection

Condition
Breast Cancer
Intervention / Treatment

-

Contacts and Locations

Philadelphia

Sidney Kimmel Cancer Center at Thomas Jefferson University, Philadelphia, Pennsylvania, United States, 19107

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

  • * Adults \>18 years old at time of consent
  • * Subject must be capable to giving informed consent or have an acceptable surrogate capable of giving consent on the subject behalf.
  • * Patients with carcinoma in situ or invasive breast cancer
  • * Patient must be undergoing one of the following:
  • * definitive surgical tumor resection for breast cancer OR
  • * placement of a vascular access device as a prelude to neoadjuvant therapy for breast cancer OR
  • * neurosurgical resection of a brain metastasis from primary breast cancer.
  • * \<18 years old
  • * Not able to give informed consent and does not have acceptable surrogate capable to giving informed consent.
  • * Active drug/alcohol dependence or abuse history

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Thomas Jefferson University,

Nicole Simone, MD, PRINCIPAL_INVESTIGATOR, Sidney Kimmel Cancer Center at Thomas Jefferson University

Study Record Dates

2028-08-11