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Breast Elasticity Imaging During Neoadjuvant Chemotherapy

Primary Purpose

Breast Cancer

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Harmonic motion imaging
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Breast Cancer focused on measuring Breast cancer, Neoadjuvant chemotherapy, Harmonic Motion Imaging (HMI), Ultrasound

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women age ≥18
  • Deemed eligible to receive neoadjuvant systemic therapy as per the treating physician, with the dose and schedule deemed appropriate by the treating physician.
  • Any stage invasive breast cancer provided the primary breast tumor size is ≥ 4 mm

Exclusion criteria:

  • Patient is pregnant or lactating
  • Presence of breast implants
  • History of laser or radiation therapy to the affected breast

Sites / Locations

  • Columbia University Irving Medical Center/NYPRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

HMI Group

Arm Description

Women undergoing standard neoadjuvant chemotherapy for breast cancer

Outcomes

Primary Outcome Measures

Assessment of the correlation between change in HMI measurements and pathologic response at completion of neoadjuvant therapy
Repeated measures analysis of variance (ANOVA) will be performed to investigate the overall differences in HMI measurements within the tumor and surrounding tissue between responders (pCR and RCB1) and non-responders (RCB2). This relative percent change in tumor stiffness is directly related to HMI measurements. Pathologic response will be assessed by the Residual Cancer Burden (RCB) score, a continuous and categorical measure of pathologic response and an independent predictor of disease free survival. Pathologic response will be dichotomized, with response defined as a score of 0-1 (RCB<2), and no response defined as a score of 2-3 (RCB2).
Assessment of the correlation between change in HMI measurements and pathologic response during neoadjuvant systemic therapy
Repeated measures analysis of variance (ANOVA) will be performed to investigate the overall differences in HMI measurements within the tumor and surrounding tissue between responders (pCR and RCB1) and non-responders (RCB2). This relative percent change in tumor stiffness is directly related to HMI measurements. Pathologic response will be assessed by the Residual Cancer Burden (RCB) score, a continuous and categorical measure of pathologic response and an independent predictor of disease free survival. Pathologic response will be dichotomized, with response defined as a score of 0-1 (RCB<2), and no response defined as a score of 2-3 (RCB2).

Secondary Outcome Measures

Assessment of correlation between percent change of tumor size on breast ultrasound and pathologic response at treatment completion
The investigator will use the statistic Z=(f1-f2)/se where fi= .5ln[(1+ri)/(1-ri)](Fisher transformation of ri), ri is the sample correlation coefficient of Ri and se is the standard error of f1-f2. The investigator will compare Z with standard normal distribution.
Assessment of correlation between percent change of tumor size on breast ultrasound during treatment
The investigator will use the statistic Z=(f1-f2)/se where fi= .5ln[(1+ri)/(1-ri)](Fisher transformation of ri), ri is the sample correlation coefficient of Ri and se is the standard error of f1-f2. The investigator will compare Z with standard normal distribution.

Full Information

First Posted
March 8, 2021
Last Updated
August 29, 2023
Sponsor
Columbia University
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT04824027
Brief Title
Breast Elasticity Imaging During Neoadjuvant Chemotherapy
Official Title
Predicting Response to Neoadjuvant Chemotherapy Using Harmonic Motion Imaging in Women With Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 14, 2021 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
National Cancer Institute (NCI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
For this study, the investigators propose investigation of a new imaging technique, Harmonic Motion Imaging (HMI), and the evaluation of its potential role in prediction of breast cancer response to neoadjuvant chemotherapy (NACT). The investigators hypothesize that changes in HMI parameters will predict response to neoadjuvant systemic therapy in early-stage breast cancer.
Detailed Description
Neoadjuvant chemotherapy (NACT) is the standard of care for treatment of locally advanced breast cancer (LABC) and inflammatory breast cancer, and is recently being used in earlier stage breast cancer. The ideal outcome of NACT is pathological complete response (pCR), which itself has shown to be associated with improved disease-free survival. However, pCR is currently determined at the time of the surgery when the patient has received the whole cycle of the treatment. Early detection of non-responders to NACT could be used to halt ineffective treatment and start a new chemotherapeutic regimen in order to achieve better tumor response and overall survival. Current techniques to monitor response to NACT based on tumor size changes include mammography, physical examination, ultrasonography and MRI. Clinically assessing tumor size has been shown to be only moderately useful for chemotherapy response prediction in these patients because tumor shrinkage is a late marker of effective treatment. Metabolic activities and microstructure changes induced by NACT can be determined using functional imaging methods such as PET-CT, contrast enhanced MRI and diffuse optical spectroscopy. However, the application of these methods is limited due to high cost and intravenous injection of exogenous contrast agents. Limited studies have shown the potential of ultrasound elastography to be useful in predicting and monitoring response to NACT in breast cancer tumors based on tumor stiffness. Harmonic Motion Imaging (HMI) is a novel ultrasound elastography technique that applies an oscillatory force locally and at different depths in the tissue, in order to determine the characteristics of the resulting localized harmonic motion using high precision tracking methods. Highly localized harmonic motion can be noninvasively generated by ultrasonic beams deep inside the tissue and estimated at high precision, by using RF signals and cross-correlation methods. In addition to not being burdened by the drawbacks encountered by existing techniques, due to the highly localized and harmonic nature of the response, the motion characteristics can be directly linked to the local tissue stiffness. In this study, the investigators propose to compare the changes in the measurements provided by HMI and pathological response rate, between baseline, during treatment and end of the treatment to assess whether HMI can early predict the tumor response to neoadjuvant therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Breast cancer, Neoadjuvant chemotherapy, Harmonic Motion Imaging (HMI), Ultrasound

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HMI Group
Arm Type
Experimental
Arm Description
Women undergoing standard neoadjuvant chemotherapy for breast cancer
Intervention Type
Procedure
Intervention Name(s)
Harmonic motion imaging
Other Intervention Name(s)
HMI technique
Intervention Description
Harmonic motion imaging (HMI) is a non-invasive ultrasound elasticity imaging technique that yields a quantitative relative measurement of tissue stiffness suitable for comparisons between individuals and over time. This technique induces dynamic tissue vibrations internally for tissue elasticity characterization. Participants will be asked to lie down on their back, hold still with shallow breathing while pictures/images are taken of the breast where the tumor is located using an ultrasound without any invasive procedures.
Primary Outcome Measure Information:
Title
Assessment of the correlation between change in HMI measurements and pathologic response at completion of neoadjuvant therapy
Description
Repeated measures analysis of variance (ANOVA) will be performed to investigate the overall differences in HMI measurements within the tumor and surrounding tissue between responders (pCR and RCB1) and non-responders (RCB2). This relative percent change in tumor stiffness is directly related to HMI measurements. Pathologic response will be assessed by the Residual Cancer Burden (RCB) score, a continuous and categorical measure of pathologic response and an independent predictor of disease free survival. Pathologic response will be dichotomized, with response defined as a score of 0-1 (RCB<2), and no response defined as a score of 2-3 (RCB2).
Time Frame
Baseline and through neoadjuvant therapy completion (an average of 28 weeks)
Title
Assessment of the correlation between change in HMI measurements and pathologic response during neoadjuvant systemic therapy
Description
Repeated measures analysis of variance (ANOVA) will be performed to investigate the overall differences in HMI measurements within the tumor and surrounding tissue between responders (pCR and RCB1) and non-responders (RCB2). This relative percent change in tumor stiffness is directly related to HMI measurements. Pathologic response will be assessed by the Residual Cancer Burden (RCB) score, a continuous and categorical measure of pathologic response and an independent predictor of disease free survival. Pathologic response will be dichotomized, with response defined as a score of 0-1 (RCB<2), and no response defined as a score of 2-3 (RCB2).
Time Frame
Baseline and during short-interval on treatment (approximately 4 weeks after treatment initiation)
Secondary Outcome Measure Information:
Title
Assessment of correlation between percent change of tumor size on breast ultrasound and pathologic response at treatment completion
Description
The investigator will use the statistic Z=(f1-f2)/se where fi= .5ln[(1+ri)/(1-ri)](Fisher transformation of ri), ri is the sample correlation coefficient of Ri and se is the standard error of f1-f2. The investigator will compare Z with standard normal distribution.
Time Frame
Baseline and through neoadjuvant therapy completion (an average of 28 weeks)
Title
Assessment of correlation between percent change of tumor size on breast ultrasound during treatment
Description
The investigator will use the statistic Z=(f1-f2)/se where fi= .5ln[(1+ri)/(1-ri)](Fisher transformation of ri), ri is the sample correlation coefficient of Ri and se is the standard error of f1-f2. The investigator will compare Z with standard normal distribution.
Time Frame
Baseline and during short-interval on treatment (approximately 4 weeks after treatment initiation)
Other Pre-specified Outcome Measures:
Title
Assessment of correlation between change in Ki-67 and change in HMI
Description
This will be analyzed using Fisher transformation.
Time Frame
Baseline and through neoadjuvant therapy completion (an average of 28 weeks)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women age ≥18 Deemed eligible to receive neoadjuvant systemic therapy as per the treating physician, with the dose and schedule deemed appropriate by the treating physician. Any stage invasive breast cancer provided the primary breast tumor size is ≥ 4 mm Exclusion criteria: Patient is pregnant or lactating Presence of breast implants History of laser or radiation therapy to the affected breast
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elisa Konofagou, PhD
Phone
212-342-1612
Email
ek2191@columbia.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Yangpei Liu, MSc
Phone
212-342-1612
Email
yl4786@columbia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elisa Konofagou, PhD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Irving Medical Center/NYP
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elisa Konofagou, PhD
Phone
212-342-1612
Email
ek2191@columbia.edu
First Name & Middle Initial & Last Name & Degree
Yangpei Liu, MSc
Phone
212-342-1612
Email
yl4786@columbia.edu
First Name & Middle Initial & Last Name & Degree
Elisa Konofagou, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No individual participant data (IPD) will be shared with other researchers.
Citations:
PubMed Identifier
32943648
Citation
Saharkhiz N, Ha R, Taback B, Li XJ, Weber R, Nabavizadeh A, Lee SA, Hibshoosh H, Gatti V, Kamimura HAS, Konofagou EE. Harmonic motion imaging of human breast masses: an in vivo clinical feasibility. Sci Rep. 2020 Sep 17;10(1):15254. doi: 10.1038/s41598-020-71960-5.
Results Reference
background
PubMed Identifier
33523806
Citation
Hossain MM, Saharkhiz N, Konofagou EE. Feasibility of Harmonic Motion Imaging Using a Single Transducer: In Vivo Imaging of Breast Cancer in a Mouse Model and Human Subjects. IEEE Trans Med Imaging. 2021 May;40(5):1390-1404. doi: 10.1109/TMI.2021.3055779. Epub 2021 Apr 30.
Results Reference
background
PubMed Identifier
21767903
Citation
Meng W, Zhang G, Wu C, Wu G, Song Y, Lu Z. Preliminary results of acoustic radiation force impulse (ARFI) ultrasound imaging of breast lesions. Ultrasound Med Biol. 2011 Sep;37(9):1436-43. doi: 10.1016/j.ultrasmedbio.2011.05.022. Epub 2011 Jul 20.
Results Reference
background
Links:
URL
https://ueil.bme.columbia.edu/
Description
Ultrasound Elasticity Imaging Laboratory - Columbia University

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Breast Elasticity Imaging During Neoadjuvant Chemotherapy

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