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Soy Isoflavones and Breast Cancer Risk Reduction

Primary Purpose

Breast Cancer

Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
isoflavones
carbohydrate
Sponsored by
The University of Texas Medical Branch, Galveston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring soy, isoflavones, phytoestrogens, prevention, mammographic density, bone density

Eligibility Criteria

30 Years - 42 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: healthy premenopausal women 30 to 42 years old normal mammograms regular menstrual cycles Exclusion Criteria: abnormal mammograms first degree relatives with breast cancer pregnant or lactating peri- or post-menopause breast augmentation, reduction or lifting on oral contraceptive medications or exogenous hormones medically prescribed diets allergic reaction to soy products

Sites / Locations

  • General Clinical Reserach Center, The University of Texas Medical Branch

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

soy isoflavones

carbohydrates (maltodextrin)

Outcomes

Primary Outcome Measures

Breast density
Amount or percentage of fibroglandular breast tissue in a breast as measured by digital mammography or by magnetic resonance imaging

Secondary Outcome Measures

bone density
Bone mineral density of whole body, hip and spine as measured by dual x-ray absorptiometry

Full Information

First Posted
September 12, 2005
Last Updated
January 30, 2023
Sponsor
The University of Texas Medical Branch, Galveston
Collaborators
National Cancer Institute (NCI), National Center for Research Resources (NCRR)
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1. Study Identification

Unique Protocol Identification Number
NCT00204490
Brief Title
Soy Isoflavones and Breast Cancer Risk Reduction
Official Title
Mammographic Density and Soy Isoflavones
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 2004 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Texas Medical Branch, Galveston
Collaborators
National Cancer Institute (NCI), National Center for Research Resources (NCRR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Soy consumption has been associated with reduced risk for developing breast cancer. Soy contains isoflavones which are weak estrogens. The roles of soy isoflavones in reducing breast cancer risk are currently unclear. Breast density has been considered as a breast cancer risk marker. We hypothesize that because isoflavones have estrogen-like activities, breast density and possibly bone density will be lower in women on soy-isoflavones.
Detailed Description
This is a randomized, double-blind study, with two arms and 100 women in each arm. Premenopausal women will be recruited and randomly allocated to take one of the two different dietary supplements in pills daily for 2 years. The two supplements are soy isoflavones (treatment) and placebo (carbohydrates). Both treatment and placebo pills will contain multi-vitamins and minerals. Multiple blood, urine, and breast fluid samples will be obtained before and during the dietary supplement periods and analyzed for biomarkers of breast cancer risk. At baseline and after the intervention period, breast density and bone density will be assessed by radiologic techniques. The efficacy of the dietary intervention will be determined by comparing mean changes of serum markers for breast cancer risk,dense breast tissue, and bone mineral density over the two year dietary intervention period in the two supplement groups with adjustment for baseline values and individual patient characteristics of interest. We predict that 2 years of soy isoflavone supplement will reduce breast density, which may be explained by individual changes in serum markers of breast cancer risk.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
soy, isoflavones, phytoestrogens, prevention, mammographic density, bone density

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
One group received soy isoflavones (60 mg daidzein, 60 mg gensitein and 16.6 mg glycitein, all as aglycone equivalent) Another group, carbohydrate filler
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Research pharmacist dispensed study pills according to a pre-generated randomization list and were blinded to all other aspects of the study protocol. Subjects, research staff, investigators, and statistician all were blinded to treatment assignment.
Allocation
Randomized
Enrollment
197 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
soy isoflavones
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
carbohydrates (maltodextrin)
Intervention Type
Dietary Supplement
Intervention Name(s)
isoflavones
Other Intervention Name(s)
Isoflavone pill
Intervention Description
soy isoflavones: Each tablet contains 246 mg Novasoy, 676 mg calcium, 15 mg riboflavin, and other innert materials to a total weight of 1000 mg. Subject takes two isoflavone tablets plus 1 multi-vitamin per day for five days per week for upto 2 years.
Intervention Type
Dietary Supplement
Intervention Name(s)
carbohydrate
Other Intervention Name(s)
Sugar pill
Intervention Description
carbohydrate: 246 mg maltodextrin, 676 mg calcium, 15 mg riboflavin and other innert ingredients to a total weight of 1000 mg per tablet. subject takes two tablets plus one multivitamin per day for five days per week for upto 2 years.
Primary Outcome Measure Information:
Title
Breast density
Description
Amount or percentage of fibroglandular breast tissue in a breast as measured by digital mammography or by magnetic resonance imaging
Time Frame
one or two years after dietary supplements
Secondary Outcome Measure Information:
Title
bone density
Description
Bone mineral density of whole body, hip and spine as measured by dual x-ray absorptiometry
Time Frame
one or two years after dietary supplement

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy premenopausal women 30 to 42 years old normal mammograms regular menstrual cycles Exclusion Criteria: abnormal mammograms first degree relatives with breast cancer pregnant or lactating peri- or post-menopause breast augmentation, reduction or lifting on oral contraceptive medications or exogenous hormones medically prescribed diets allergic reaction to soy products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lee-Jane W Lu, Ph.D.
Organizational Affiliation
The University of Teas Medical Branch
Official's Role
Principal Investigator
Facility Information:
Facility Name
General Clinical Reserach Center, The University of Texas Medical Branch
City
Galveston
State/Province
Texas
ZIP/Postal Code
77555-0264
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
31535213
Citation
Lu LW, Chen NW, Nayeem F, Nagamani M, Anderson KE. Soy isoflavones interact with calcium and contribute to blood pressure homeostasis in women: a randomized, double-blind, placebo controlled trial. Eur J Nutr. 2020 Sep;59(6):2369-2381. doi: 10.1007/s00394-019-02085-3. Epub 2019 Sep 18.
Results Reference
derived
PubMed Identifier
29183775
Citation
Lu LW, Chen NW, Nayeem F, Ramanujam VS, Kuo YF, Brunder DG, Nagamani M, Anderson KE. Novel effects of phytoestrogenic soy isoflavones on serum calcium and chloride in premenopausal women: A 2-year double-blind, randomized, placebo-controlled study. Clin Nutr. 2018 Dec;37(6 Pt A):1862-1870. doi: 10.1016/j.clnu.2017.11.002. Epub 2017 Nov 11.
Results Reference
derived
PubMed Identifier
23044556
Citation
Lu LJ, Nishino TK, Johnson RF, Nayeem F, Brunder DG, Ju H, Leonard MH, Grady JJ, Khamapirad T. Comparison of breast tissue measurements using magnetic resonance imaging, digital mammography and a mathematical algorithm. Phys Med Biol. 2012 Nov 7;57(21):6903-27. doi: 10.1088/0031-9155/57/21/6903. Epub 2012 Oct 9.
Results Reference
derived

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Soy Isoflavones and Breast Cancer Risk Reduction

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