Contrast Enhanced Ultrasound and Shear Wave Elastography in Measuring Response in Patients With Breast Cancer Receiving Chemotherapy Before Surgery
Primary Purpose
Breast Cancer
Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
dynamic contrast-enhanced ultrasound imaging
shear wave elastography
Definity, (Lipid Microspheres) Intravenous Suspension
Philips Shear Wave Elastography
Sponsored by

About this trial
This is an interventional diagnostic trial for Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- Women with histologically confirmed breast cancer (by core needle biopsy)
- Women with >= 2 cm clinically or radiologically measureable breast cancer
- Women scheduled to receive neoadjuvant chemotherapy as part of their treatment plan
- Women competent to sign study specific written Informed Consent
- Women willing to comply with protocol requirements
Exclusion Criteria:
- Women who are pregnant
- Women who have undergone open surgical (excisional) biopsy for breast cancer diagnosis
- Women who have had a prior history of breast cancer in the same breast
- Women with known cardiac shunt, pulmonary hypertension or hypersensitivity to perflutren agent
- Women who cannot consent for themselves
Sites / Locations
- USC Norris Comprehensive Cancer Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Diagnostic (CEUS, SWE)
Arm Description
Patients undergo dynamic contrast-enhanced ultrasound imaging and shear wave elastography at baseline, 2-3 weeks after initiation of chemotherapy, and before surgery.
Outcomes
Primary Outcome Measures
Model predicted treatment response for CEUS and SWE
Weighted Kappa will be used to assess the agreement.
Pathologically determined treatment response for CEUS and SWE
Weighted Kappa will be used to assess the agreement.
Secondary Outcome Measures
Treatment response predicted by novel ultrasound techniques
Weighted Kappa will be used to assess the agreement. Scatter plots and contingency tables will be used to identify discordant cases between US techniques and CE MRI.
Treatment response predicted by CE MRI
Weighted Kappa will be used to assess the agreement. Scatter plots and contingency tables will be used to identify discordant cases between US techniques and CE MRI.
Full Information
NCT ID
NCT02067884
First Posted
February 4, 2014
Last Updated
January 23, 2019
Sponsor
University of Southern California
Collaborators
National Cancer Institute (NCI), L K Whittier Foundation
1. Study Identification
Unique Protocol Identification Number
NCT02067884
Brief Title
Contrast Enhanced Ultrasound and Shear Wave Elastography in Measuring Response in Patients With Breast Cancer Receiving Chemotherapy Before Surgery
Official Title
Real Time Contrast Enhanced Ultrasound and Ultrasound-Based Elastography: Novel Techniques in Assessment of Treatment Response to Neoadjuvant Chemotherapy for Breast Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Terminated
Why Stopped
Slow accrual
Study Start Date
December 19, 2013 (Actual)
Primary Completion Date
September 25, 2016 (Actual)
Study Completion Date
September 25, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Southern California
Collaborators
National Cancer Institute (NCI), L K Whittier Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This pilot clinical trial studies contrast enhanced ultrasound and shear wave elastography in measuring response in patients with breast cancer receiving chemotherapy before surgery. New imaging procedures, such as contrast enhanced ultrasound and shear wave elastography, may predict treatment response earlier and more accurately than contrast enhanced magnetic resonance imaging.
Detailed Description
PRIMARY OBJECTIVES:
I. To establish a quantitative prediction rule for accurate and early prediction of the pathologic tumor response assessed post-surgery, using the change of contrast enhanced ultrasound (CEUS) assessed tumor size and perfusion characteristics before (baseline) and 2-3 weeks following initiation of neoadjuvant chemotherapy (NAC).
II. To assess the agreement between CEUS based classification rule and pathologically determined treatment response (baseline versus pre-surgical scan).
III. To establish a quantitative prediction rule for accurate and early prediction of the pathologic tumor response assessed post-surgery, using the change in propagation velocity of a shear mechanical wave in tissue before (baseline) and 2-3 weeks following initiation of NAC.
IV. To assess the agreement between shear wave elastography (SWE) based classification rule and pathologically determined treatment response (baseline versus pre-surgical scan).
SECONDARY OBJECTIVES:
I. To explore the role of combined CEUS + SWE features obtained at early treatment phase (2-3 weeks following initiation of NAC), in accurately predicting the pathologically determined tumor response.
II. To investigate the agreement in assessment of therapy response to NAC between CEUS versus contrast enhanced magnetic resonance imaging (CE MRI) and SWE versus CE MRI for baseline versus pre-surgery scan and to identify discordant cases using scatter plot and contingency tables.
OUTLINE:
Patients undergo dynamic contrast-enhanced ultrasound imaging and shear wave elastography at baseline, 2-3 weeks after initiation of chemotherapy, and before surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
34 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Diagnostic (CEUS, SWE)
Arm Type
Experimental
Arm Description
Patients undergo dynamic contrast-enhanced ultrasound imaging and shear wave elastography at baseline, 2-3 weeks after initiation of chemotherapy, and before surgery.
Intervention Type
Procedure
Intervention Name(s)
dynamic contrast-enhanced ultrasound imaging
Other Intervention Name(s)
DCE-USI
Intervention Description
Undergo CEUS
Intervention Type
Procedure
Intervention Name(s)
shear wave elastography
Other Intervention Name(s)
SWE
Intervention Description
Undergo SWE
Intervention Type
Drug
Intervention Name(s)
Definity, (Lipid Microspheres) Intravenous Suspension
Other Intervention Name(s)
Perflutren Lipid Microsphere
Intervention Description
Participant will receive contrast agent by intravenous administration
Intervention Type
Device
Intervention Name(s)
Philips Shear Wave Elastography
Other Intervention Name(s)
Shear Wave Elastography
Intervention Description
Equipment used for SWE
Primary Outcome Measure Information:
Title
Model predicted treatment response for CEUS and SWE
Description
Weighted Kappa will be used to assess the agreement.
Time Frame
Up to 1 year
Title
Pathologically determined treatment response for CEUS and SWE
Description
Weighted Kappa will be used to assess the agreement.
Time Frame
Up to 1 year
Secondary Outcome Measure Information:
Title
Treatment response predicted by novel ultrasound techniques
Description
Weighted Kappa will be used to assess the agreement. Scatter plots and contingency tables will be used to identify discordant cases between US techniques and CE MRI.
Time Frame
Up to 1 year
Title
Treatment response predicted by CE MRI
Description
Weighted Kappa will be used to assess the agreement. Scatter plots and contingency tables will be used to identify discordant cases between US techniques and CE MRI.
Time Frame
Up to 1 year
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women with histologically confirmed breast cancer (by core needle biopsy)
Women with >= 2 cm clinically or radiologically measureable breast cancer
Women scheduled to receive neoadjuvant chemotherapy as part of their treatment plan
Women competent to sign study specific written Informed Consent
Women willing to comply with protocol requirements
Exclusion Criteria:
Women who are pregnant
Women who have undergone open surgical (excisional) biopsy for breast cancer diagnosis
Women who have had a prior history of breast cancer in the same breast
Women with known cardiac shunt, pulmonary hypertension or hypersensitivity to perflutren agent
Women who cannot consent for themselves
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Linda Hovanessian-Larsen
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
USC Norris Comprehensive Cancer Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Contrast Enhanced Ultrasound and Shear Wave Elastography in Measuring Response in Patients With Breast Cancer Receiving Chemotherapy Before Surgery
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