Actively Recruiting

Age: 18Years +
All Genders
NCT05704062

Quantitative MRI Assessment of Breast Cancer Therapy Response

Led by Corewell Health East · Updated on 2026-04-17

135

Participants Needed

4

Research Sites

897 weeks

Total Duration

On this page

Sponsors

C

Corewell Health East

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to investigate and validate multi-parametric magnetic resonance imaging (MRI) modalities for assessment of breast cancer response to neoadjuvant chemotherapy in a multi-site and multi-MRI scanner platform setting. This study is conducted at Oregon Health \& Science University (OHSU), University of Washington (UW), and University of Iowa (UI) using Siemens, Philips, and General Electric MRI scanners, respectively. MRI is a type of scan that uses a very strong magnet and no radiation to take very detailed pictures of parts of the body. MRI is often used as standard of care to take pictures of breast tumor(s) before and after chemotherapy treatment in order to measure the tumor size changes in response to treatment, and in order to plan for surgery. MRI is used because the images it takes are very clear and the borders of the tumor can be measured very accurately. However the tumor size alone is often not a good early indicator of whether or not the tumor responds to treatment. Tumor size change usually happens late during the period of treatment, and tumor size measured with MRI after treatment can overestimate or underestimate the residual cancer. This makes it difficult to do the right surgical planning. In addition to measuring tumor size, the MRI scans in this research study will also measure changes in tumor blood vessels and the number of cancer cells per unit of tumor volume. The purpose of this study is to see whether MRI measurements of these functional tumor properties provide better early prediction and evaluation of breast cancer response to neoadjuvant chemotherapy than tumor size measurement. This is an observational study because the MRI procedures are not expected to have an effect on health outcomes. Eligible participants on this study are receiving standard of care neoadjuvant treatment for their cancer.

CONDITIONS

Official Title

Quantitative MRI Assessment of Breast Cancer Therapy Response

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with confirmed breast cancer scheduled for standard neoadjuvant chemotherapy before surgery
  • No contraindications for MRI exams
  • Normal kidney function to safely receive gadolinium-based MRI contrast agent
  • Not pregnant
  • Able to understand and willing to sign informed consent
Not Eligible

You will not qualify if you...

  • Presence of pacemaker, aneurysm clip, or other conditions preventing MRI
  • Unable to cooperate for a 45-minute MRI or allergic to gadolinium contrast agent
  • Severe claustrophobia preventing MRI
  • Acute or chronic kidney dysfunction (eGFR < 60 ml/min/1.73 m2)
  • Pregnant participants
  • Cognitive impairment

AI-Screening

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Trial Site Locations

Total: 4 locations

1

University of Iowa

Iowa City, Iowa, United States, 52242

Actively Recruiting

2

Corewell Health William Beaumont University Hospital

Royal Oak, Michigan, United States, 48073

Actively Recruiting

3

OHSU Knight Cancer Institute

Portland, Oregon, United States, 97239

Completed

4

University of Washington

Seattle, Washington, United States, 98109

Actively Recruiting

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Research Team

W

Wei Huang, Chief, MR Rad Imaging Physics, PhD

CONTACT

K

Kristen Grant, RN

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Quantitative MRI Assessment of Breast Cancer Therapy Response | DecenTrialz