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

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NYU Langone Health

Status

Enrolling

Conditions

Breast Cancer

Treatments

Diagnostic Test: Diagnostic Breast Cancer Scan
Diagnostic Test: Research Scan for Gradient-echo Spectroscopic Imaging (GSI)

Study type

Interventional

Funder types

Other

Identifiers

NCT03400215
17-01549

Details and patient eligibility

About

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.

Full description

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.

Enrollment

135 estimated patients

Sex

Female

Ages

25 to 99 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

135 participants in 2 patient groups

Breast cancer confirmed by biopsy
Active Comparator group
Description:
Cases will be women first diagnosed with invasive breast cancer confirmed by biopsy
Treatment:
Diagnostic Test: Research Scan for Gradient-echo Spectroscopic Imaging (GSI)
Diagnostic Test: Diagnostic Breast Cancer Scan
Women without any history of breast cancer
Active Comparator group
Description:
No known malignancy confirmed by at least 1-year follow up exams.
Treatment:
Diagnostic Test: Research Scan for Gradient-echo Spectroscopic Imaging (GSI)
Diagnostic Test: Diagnostic Breast Cancer Scan

Trial contacts and locations

1

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Central trial contact

Reshma Gadde; Samuel Brazil

Data sourced from clinicaltrials.gov

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