Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue: A Randomized Placebo Controlled Study

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Memorial Sloan-Kettering Cancer Center
ClinicalTrials.gov Identifier:
NCT00597532
First received: December 26, 2007
Last updated: January 31, 2013
Last verified: January 2013

December 26, 2007
January 31, 2013
August 2002
June 2014   (final data collection date for primary outcome measure)
The primary outcome of the study is comparison of the change in proliferation (Ki67) and apoptosis (TUNEL) in cancerous tissue between the 2 groups. [ Time Frame: Conclusion of the study ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00597532 on ClinicalTrials.gov Archive Site
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Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue: A Randomized Placebo Controlled Study
Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue: A Randomized Placebo Controlled Study

To Test Effect of Soy Supplementation on Cellular Markers in Normal and Cancerous Breast Tissue using a Randomized Placebo Controlled Study.

Objectives:

  • To determine (by immunohistochemistry) whether specific cellular markers and gene products associated with breast carcinoma can be altered by soy therapy.
  • To identify genes that can be altered by soy therapy in normal and neoplastic breast tissues by unbiased gene expression analysis using microarrays.
  • To compare specific cellular markers and pathways (immunohistochemistry), and gene expression using microarrays in normal and cancerous breast tissue.

Patient Population:

Pre and post menopausal women with breast cancer diagnosed by core needle biopsy scheduled to undergo breast cancer resection for an invasive carcinoma.

Objectives:

  • To determine (by immunohistochemistry) whether specific cellular markers and gene products associated with breast carcinoma can be altered by soy therapy.
  • To identify genes that can be altered by soy therapy in normal and neoplastic breast tissues by unbiased gene expression analysis using microarrays.
  • To compare specific cellular markers and pathways (immunohistochemistry), and gene expression using microarrays in normal and cancerous breast tissue.

Study Design and Intervention Plan:

  • Eligible patients will be consented at the time of visit with MSKCC breast surgeon and randomized to receive soy (soy protein supplementation 50 grams/day), or placebo (milk protein supplementation 50 grams/day) over the period until their surgery.
  • The diagnostic biopsy (already available at time of appointment with MSKCC surgeon) will be analyzed by immunohistochemistry for proliferation (Ki67) and apoptosis (TUNEL). Additional immunohistochemistry will include HER2, TP53, cyclin D1, p27, BCL2, ER and PR.
  • Excision of the breast carcinoma (lumpectomy or mastectomy) will proceed in standard fashion.
  • The post-therapy excision specimen will be processed in a standard fashion. Pathologic features, margin status, and tumor size will be assessed by a light microscopic examination of histological sections. In addition to this routine processing, immunohistochemistry assays for proliferation (Ki67), apoptosis (TUNEL), HER2, TP53, cyclin D1, p27, BCL2, ER, and PR will be performed. For correlative biological studies pathologists will select approximately .5 cubic mm representative sections of the neoplastic tissues and normal adjacent breast tissue, which will be snap frozen for gene expression analysis using microarrays.
Interventional
Phase 0
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Diagnostic
Breast Cancer
  • Dietary Supplement: Soy
    soy (soy protein supplementation 50 grams/day)
  • Dietary Supplement: Milk
    placebo (milk protein supplementation 50 grams/day)
  • Experimental: 1
    soy (soy protein supplementation 50 grams/day)
    Intervention: Dietary Supplement: Soy
  • Placebo Comparator: 2
    milk protein supplementation 50 grams/day
    Intervention: Dietary Supplement: Milk
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
140
August 2014
June 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Informed consent obtained
  • Breast mass > .5 cm (determined by mammogram, ultrasound, MRI, or palpable criteria)
  • Core biopsy diagnosis of invasive carcinoma of the breast

Exclusion Criteria:

  • History of active malignancy within previous two years (except for non-melanoma skin cancer and history of breast cancer).
  • Regular soy consumption (consumption of more than 3 serving of soy or soy products/supplements per week)
  • Allergy to soy or milk protein
Female
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00597532
02-062
Not Provided
Memorial Sloan-Kettering Cancer Center
Memorial Sloan-Kettering Cancer Center
Not Provided
Principal Investigator: Moshe Shike, MD Memorial Sloan-Kettering Cancer Center
Memorial Sloan-Kettering Cancer Center
January 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP