Breast Elasticity Imaging During Neoadjuvant Chemotherapy

Sponsor
Columbia University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04824027
Collaborator
National Cancer Institute (NCI) (NIH)
50
1
1
18.6
2.7

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Harmonic motion imaging
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Predicting Response to Neoadjuvant Chemotherapy Using Harmonic Motion Imaging in Women With Breast Cancer
Actual Study Start Date :
Jun 14, 2021
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Jan 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: HMI Group

Women undergoing standard neoadjuvant chemotherapy for breast cancer

Procedure: Harmonic motion imaging
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.
Other Names:
  • HMI technique
  • Outcome Measures

    Primary Outcome Measures

    1. Assessment of the correlation between change in HMI measurements and pathologic response at completion of neoadjuvant therapy [Baseline and through neoadjuvant therapy completion (an average of 28 weeks)]

      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).

    2. Assessment of the correlation between change in HMI measurements and pathologic response during neoadjuvant systemic therapy [Baseline and during short-interval on treatment (approximately 4 weeks after treatment initiation)]

      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

    1. Assessment of correlation between percent change of tumor size on breast ultrasound and pathologic response at treatment completion [Baseline and through neoadjuvant therapy completion (an average of 28 weeks)]

      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.

    2. Assessment of correlation between percent change of tumor size on breast ultrasound during treatment [Baseline and during short-interval on treatment (approximately 4 weeks after treatment initiation)]

      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.

    Other Outcome Measures

    1. Assessment of correlation between change in Ki-67 and change in HMI [Baseline and through neoadjuvant therapy completion (an average of 28 weeks)]

      This will be analyzed using Fisher transformation.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Columbia University Irving Medical Center/NYP New York New York United States 10032

    Sponsors and Collaborators

    • Columbia University
    • National Cancer Institute (NCI)

    Investigators

    • Principal Investigator: Elisa Konofagou, PhD, Columbia University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Elisa Konofagou, Robert and Margaret Hariri Professor in Biomedical Engineering and Radiology, Columbia University
    ClinicalTrials.gov Identifier:
    NCT04824027
    Other Study ID Numbers:
    • AAAT4412
    • R01CA228275
    First Posted:
    Apr 1, 2021
    Last Update Posted:
    Nov 3, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Elisa Konofagou, Robert and Margaret Hariri Professor in Biomedical Engineering and Radiology, Columbia University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 3, 2021