Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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
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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