Gradient-Echo Spectroscopic Imaging Study of Saturated Fat and Breast Cancer

NCT ID: NCT03400215

Last Updated: 2025-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

135 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-07-23

Study Completion Date

2025-04-17

Brief Summary

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The role of fat in breast cancer development and growth has been studied extensively using body mass index, a measure of whole body fatness, and dietary fat intake in a number of epidemiological studies. However, there is a paucity of studies, on an individual level, to assess the role of breast fat itself in breast cancer due to lack of a non-invasive and fast measurement method. Since breast fibroglandular cells are surrounded by breast fat cells, the characteristics of breast fat may have a stronger relationship with breast cancer development, as supported by recent studies showing that a majority of breast cancer develops at the interface between fibroglandular tissue and adipose tissue. However, it is not trivial to study the role of breast fat, mainly due to the lack of a non-invasive and fast measurement method sensitive enough to important features of breast fat, such as types of fat.Recently, we have developed a rapid MRI method, referred to as Gradient-echo Spectroscopic Imaging (GSI), to measure fatty acid composition during clinical breast MRI exams. GSI can provide map of saturated fat and unsaturated fats in the breast adipose tissue without performing tissue biopsy. Our pilot study found that the postmenopausal women with aggressive breast cancer, known as invasive ductal carcinoma, have a significantly higher percentage of saturated fat in their breast adipose tissue than the postmenopausal women with only benign lesions.

Detailed Description

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The overarching goal of this study is to determine the role of saturated fatty acid in breast cancer development and growth. In this proposal, GSI will be used for non-invasive in vivo measurement of saturated fat in the breast adipose tissue of postmenopausal women who undergo diagnostic breast MRI exams (Aims 1 and 2) or MRI-guided biopsy scans (Aim 3). The central hypotheses is that (i) the breast saturated fatty acid fraction measured by GSI is associated with the presence of malignant lesions in the breast and (ii) the breast saturated fatty acid fraction correlates positively with inflammation in the breast adipose tissue that may lead to increase in estrogen production in adipocytes.The proposed study will evaluate whether breast saturated fat is an independent risk factor for breast cancer, and whether it can provide additional diagnostic information to current clinical diagnostic exams. In addition, the proposed imaging measure of breast saturated fat can be used to assess the efficacy of any intervention to reduce cancer-related inflammation in the breast adipose tissue and to investigate the possible role of fatty acid composition in prevention and clinical management of breast cancer.

Conditions

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Breast Cancer

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Breast cancer confirmed by biopsy

Cases will be women first diagnosed with invasive breast cancer confirmed by biopsy

Group Type ACTIVE_COMPARATOR

Diagnostic Breast Cancer Scan

Intervention Type DIAGNOSTIC_TEST

clinically indicated diagnostic breast MRI scans

Research Scan for Gradient-echo Spectroscopic Imaging (GSI)

Intervention Type DIAGNOSTIC_TEST

15-min research MRI scan

Women without any history of breast cancer

No known malignancy confirmed by at least 1-year follow up exams.

Group Type ACTIVE_COMPARATOR

Diagnostic Breast Cancer Scan

Intervention Type DIAGNOSTIC_TEST

clinically indicated diagnostic breast MRI scans

Research Scan for Gradient-echo Spectroscopic Imaging (GSI)

Intervention Type DIAGNOSTIC_TEST

15-min research MRI scan

Interventions

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Diagnostic Breast Cancer Scan

clinically indicated diagnostic breast MRI scans

Intervention Type DIAGNOSTIC_TEST

Research Scan for Gradient-echo Spectroscopic Imaging (GSI)

15-min research MRI scan

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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Gradient-echo Spectroscopic Imaging

Eligibility Criteria

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Inclusion Criteria

* No contraindications to MRI scanning (pacemaker, implanted metallic objects, severe obesity or other condition that leads to difficulty lying in the magnet)
* No contraindication to gadolinium contrast agent (severe renal insufficiency (EGFR\<30), allergy to gadolinium) which will be injected for clinical exam
* Able and willing to provide informed consent
* Post-menopausal age \> 25 years.

Exclusion Criteria

* Contra-indication to MRI or gadolinium contrast agent (have a pacemaker, aneurysm clip, or other metallic implant; weigh \>135 kg; or have renal impairment)
* Breast surgery within prior 12 months, or breast implants
* Any hormonal therapy
Minimum Eligible Age

25 Years

Maximum Eligible Age

99 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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NYU Langone Health

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Linda Moy, MD

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Health

Locations

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NYU Langone Health

New York, New York, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Reshma Gadde

Role: CONTACT

6465014320

Samuel Brazil

Role: CONTACT

6465012540

Facility Contacts

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Justin Fogarty

Role: primary

212-731-5318

Other Identifiers

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17-01549

Identifier Type: -

Identifier Source: org_study_id

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