Studying Normal Breast Tissue and Cancer Risk

Sponsor
National Cancer Institute (NCI) (NIH)
Overall Status
Completed
CT.gov ID
NCT00341692
Collaborator
(none)
13
1
204.7
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Study Details

Study Description

Brief Summary

Breast cancer is the most common cancer among women in the United States. Breast cancer research has been hampered by the difficulty in collecting normal breast tissue. In this study, researchers will obtain samples of normal breast tissue from organ donors and will collect risk-factor data from next-of-kin.

The purpose of this study is to learn how normal breast develops and responds to stresses that are known to increase a woman s chance of developing breast cancer.

Following the breast-tissue donation from 20 volunteers, surgical technicians will make small incisions in the skin and tissue of the breast and remove several samples measuring about one-inch. Technicians also will take samples of the uterine lining to estimate the date of the last menstrual period. The tissue will then be sent to the National Cancer Institute for laboratory research studies. Steps will be taken to ensure that the identity of the participants remains confidential.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This pilot project, funded by a Breast Cancer Faculty Infrastructure Award, would determine the feasibility of obtaining samples of normal breast tissue from organ donors and collecting risk factor data from next-of-kin. The underlying goal of this initiative is to determine the associations between stages of breast development, risk factors for breast cancer, and gene expression. The study investigators are members of DCEG, CCR and the Transplant Resource Center of Maryland (TRC), a non-profit organization certified by HCFA and the state that processes most organ and tissue donations in Maryland. Trained staff or social workers employed by TRC who routinely obtain consent for donation from next-of-kin will also obtain consent for this study. The existing consent form for organ or tissue donation also includes informed consent for donation of tissue for research. Following organ procurement from 20 volunteers, trained surgical technicians employed by TRC who routinely assist intra-operatively, will sterilely remove tissue from each breast quadrant and split the samples; one portion will be embedded in OCT and snap frozen in liquid nitrogen and the other fixed in 10% buffered formalin. Samples of adipose tissue, blood, urine and endometrium (for menstrual dating) will also be obtained. MES in conjunction with SMH and BKV will assess the samples histopathologically and determine the quantity and quality of macromolecules (RNA, DNA, protein) contained within the tissues. Pending demonstration of the feasibility of this general approach, we will pursue additional funding for a larger study with optimized procedures. We have stopped recruiting patients.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    13 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Pilot Study to Collect Normal Breast Tissue From Organ and Tissue Donors
    Actual Study Start Date :
    Apr 7, 2003
    Actual Primary Completion Date :
    Feb 1, 2012
    Actual Study Completion Date :
    Apr 28, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Samples of normal breast tissue

    Samples of normal breast tissue from organ donors for assessment of histology.

    Outcome Measures

    Primary Outcome Measures

    1. Histological features [cross-sectional]

      descriptive

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    11 Years to 120 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    • INCLUSION CRITERIA

    The study will enroll girls or women aged 11 years or older.

    EXCLUSION CRITERIA

    Men are excluded.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Cancer Institute (NCI), 9000 Rockville Pike Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Cancer Institute (NCI)

    Investigators

    • Principal Investigator: Gretchen Benson, Ph.D., National Cancer Institute (NCI)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    National Cancer Institute (NCI)
    ClinicalTrials.gov Identifier:
    NCT00341692
    Other Study ID Numbers:
    • 999903158
    • 03-C-N158
    First Posted:
    Jun 21, 2006
    Last Update Posted:
    Apr 29, 2020
    Last Verified:
    Apr 1, 2020
    Keywords provided by National Cancer Institute (NCI)
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 29, 2020