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Positron Emission Mammography and Standard Mammography in Women at High Risk of Breast Cancer

Primary Purpose

Breast Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
questionnaire administration
digital mammography
positron emission mammography
Sponsored by
Boston Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Breast Cancer focused on measuring breast cancer

Eligibility Criteria

35 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion criteria:

DISEASE CHARACTERISTICS:

  • Scheduled to undergo screening mammogram at one of the Boston Medical Center-affiliated primary care clinics and meets 1 of the following criteria:

    • Dense breast tissue
    • At high-risk for breast cancer

PATIENT CHARACTERISTICS:

  • Has 1 of the following racial or ethnic backgrounds based on the patient's country of birth or the mother and father's country of birth:

    • Hispanic
    • Haitian Creole
    • African American
    • Caucasian

PRIOR CONCURRENT THERAPY:

  • None specified

Exclusion criteria:

  • No history of breast cancer, palpable breast mass, abnormal nipple discharge, or other focal complaints warranting diagnostic mammogram

Sites / Locations

  • Boston University Cancer Research Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

positron emission mammography

Arm Description

questionnaire administration digital mammography positron emission mammography

Outcomes

Primary Outcome Measures

Frequency of Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" Call-back in Mammography vs Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" in Positron Emission Mammography
Number of participants called back due to Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" Mammogram compared to number of patients with Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" in positron emission mammography Breast Imaging Assessment Reporting and Data System (BI-RADS) Scale: 0 = Inconclusive for malignancy; call-back in mammography = normal = abnormal, with no malignancy = abnormal, likely benign = abnormal, likely malignant = malignant

Secondary Outcome Measures

Patient Satisfaction Level as Pertaining to Comfort and Pain for Each Study
Number of participants satisfied with positron emission mammography with regard to comfort and pain for each study 1-7 rating scale, Entries from 1-4 considered Satisfied. Entries 5-7 considered not Satisfied.

Full Information

First Posted
May 9, 2009
Last Updated
April 3, 2017
Sponsor
Boston Medical Center
Collaborators
United States Department of Defense
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1. Study Identification

Unique Protocol Identification Number
NCT00896649
Brief Title
Positron Emission Mammography and Standard Mammography in Women at High Risk of Breast Cancer
Official Title
Impact of Dedicated Breast Positron Emission Mammography vs. Conventional Two-View Digital Mammography on Recall Rates and Cancer Detection as a Screening Examination in Underserved Women
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
January 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston Medical Center
Collaborators
United States Department of Defense

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Screening tests may help doctors find cancer cells early and plan better treatment for breast cancer. It is not yet known whether positron emission mammography is more effective than standard mammography in finding breast tumors. PURPOSE: This phase III trial is studying positron emission mammography to see how well it works compared with standard mammography in women undergoing screening mammogram at Boston Medical Center.
Detailed Description
OBJECTIVES: To install the breast Positron Emission Mammography system and to test and ensure its compliance with all regulatory agencies including the American College of Radiology and the Food and Drug Administration. To measure and compare the number of call-backs for positron emission mammography (PEM) imaging and conventional mammography. To measure and compare patient satisfaction for both conventional mammography and positron emission mammography in terms of comfort and pain. OUTLINE: Patients undergo a conventional two-view mammogram and positron emission mammography (PEM). Immediately following treatment, patients complete a questionnaire on their satisfaction with the standard mammogram and the positron emission mammography. After completion of study treatment, patients are followed annually.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast cancer

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
PEM
Masking
None (Open Label)
Allocation
N/A
Enrollment
193 (Actual)

8. Arms, Groups, and Interventions

Arm Title
positron emission mammography
Arm Type
Experimental
Arm Description
questionnaire administration digital mammography positron emission mammography
Intervention Type
Other
Intervention Name(s)
questionnaire administration
Intervention Description
Questionnaire regarding patient satisfaction with mammogram experience and with positron emission mammography experience.
Intervention Type
Procedure
Intervention Name(s)
digital mammography
Intervention Description
standard screening mammogram
Intervention Type
Procedure
Intervention Name(s)
positron emission mammography
Intervention Description
one-time positron emission mammography to compare recall rates with that of standard mammogram
Primary Outcome Measure Information:
Title
Frequency of Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" Call-back in Mammography vs Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" in Positron Emission Mammography
Description
Number of participants called back due to Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" Mammogram compared to number of patients with Breast Imaging Assessment Reporting and Data System (BI-RADS) "0" in positron emission mammography Breast Imaging Assessment Reporting and Data System (BI-RADS) Scale: 0 = Inconclusive for malignancy; call-back in mammography = normal = abnormal, with no malignancy = abnormal, likely benign = abnormal, likely malignant = malignant
Time Frame
immediately at completion of mammogram
Secondary Outcome Measure Information:
Title
Patient Satisfaction Level as Pertaining to Comfort and Pain for Each Study
Description
Number of participants satisfied with positron emission mammography with regard to comfort and pain for each study 1-7 rating scale, Entries from 1-4 considered Satisfied. Entries 5-7 considered not Satisfied.
Time Frame
One month

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria: DISEASE CHARACTERISTICS: Scheduled to undergo screening mammogram at one of the Boston Medical Center-affiliated primary care clinics and meets 1 of the following criteria: Dense breast tissue At high-risk for breast cancer PATIENT CHARACTERISTICS: Has 1 of the following racial or ethnic backgrounds based on the patient's country of birth or the mother and father's country of birth: Hispanic Haitian Creole African American Caucasian PRIOR CONCURRENT THERAPY: None specified Exclusion criteria: No history of breast cancer, palpable breast mass, abnormal nipple discharge, or other focal complaints warranting diagnostic mammogram
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gustavo Mercier, MD, PhD
Organizational Affiliation
Boston Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Boston University Cancer Research Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data is not useful.

Learn more about this trial

Positron Emission Mammography and Standard Mammography in Women at High Risk of Breast Cancer

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