search
Back to results

Flaxseed, Aromatase Inhibitors and Breast Tumor Characteristics (FABrC)

Primary Purpose

Breast Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Anastrozole
flaxseed
Placebo
Sponsored by
Roswell Park Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Breast Cancer focused on measuring breast neoplasms, phytoestrogens, tumor characteristics, proliferation, apoptosis, estrogen receptor, HER2

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 and ≤ 85 years
  • Postmenopausal status defined as: no menstrual cycle in the past 12 months hysterectomy with bilateral oophorectomy hysterectomy with intact ovaries if age > 55 years
  • Newly diagnosed with incident, primary, invasive, estrogen receptor positive clinical stage II or lower breast cancer
  • ECOG performance status of 1 or less
  • Willingness to comply with study guidelines and procedures
  • Willingness and ability to provide informed consent
  • Usual consumption of soy no more than 1 time per week and willingness to avoid whole soy foods or concentrated soy sources (soy milk, tofu, substitute meat products, meal replacement bars) during the intervention period
  • Willingness to avoid herbal and dietary supplements (not including vitamins), aspirin, and ibuprofen during the intervention period
  • No competing neoadjuvant or chemotherapy treatment
  • Time between pre-surgical visit and surgery must be at least 2 weeks
  • No chemotherapy in the past 12 months

Exclusion Criteria:

  • Inability to read and write English
  • Previous invasive breast cancer
  • Insulin dependent Type I or II diabetes diagnosed by physician
  • History of coagulopathy, thrombocytopenia, or bleeding disorder
  • Current (past 30 days) regular (at least once per week) use of reproductive hormone therapy, Tamoxifen, aromatase inhibitors, or other estrogen inhibitors, flaxseed, or antibiotics
  • Current chemotherapy or neoadjuvant chemotherapy
  • Allergies to flaxseed, nuts, or other seeds
  • Renal dysfunction defined as creatinine > 1.5 mg/dl
  • History of Crohns' disease, ulcerative colitis, irritable bowel syndrome, celiac sprue, or other malabsorption syndrome, diverticulitis, diverticulosis, or other bowel diagnosis which, in the opinion of the breast surgeon, would contraindicate large doses of dietary fiber or would impair nutrient absorption
  • Current, regular (more than once weekly) use of prescription blood-thinning agents including coumadin, heparin and heparin related drugs, clopidogrel bisulfate

Sites / Locations

  • Roswell Park Cancer Institute

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Placebo Comparator

Experimental

Arm Label

2

3

4

1

Arm Description

Flaxseed 25 mg per day and 1 placebo pill per day

25 mg flaxseed per day and 1 mg anastrozole pill per day

Placebo pill 1 per day

Anastrozole 1 mg pill per day

Outcomes

Primary Outcome Measures

Expression of Estrogen Receptor (ER-beta)
Mean percentage of cells expressing estrogen receptor (ER-beta)
Progesterone Receptor (PR) Expression
Mean percentage of cells expressing PR
Human Epidermal Growth Factor Receptor 2 (Her2) Expression
Mean percentage of cells expressing human epidermal growth factor receptor 2 (Her2)

Secondary Outcome Measures

Growth Hormone Serum Levels IGF-1
Mean serum level IGF-1(pg/ml)

Full Information

First Posted
February 7, 2008
Last Updated
September 11, 2017
Sponsor
Roswell Park Cancer Institute
Collaborators
National Center for Complementary and Integrative Health (NCCIH), AstraZeneca
search

1. Study Identification

Unique Protocol Identification Number
NCT00612560
Brief Title
Flaxseed, Aromatase Inhibitors and Breast Tumor Characteristics
Acronym
FABrC
Official Title
Flaxseed vs. Aromatase Inhibitors: Breast Tumor Characteristics and Prognosis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
November 2007 (undefined)
Primary Completion Date
January 2011 (Actual)
Study Completion Date
April 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Roswell Park Cancer Institute
Collaborators
National Center for Complementary and Integrative Health (NCCIH), AstraZeneca

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The proposed study plans to examine the effect of flaxseed consumption, a phytoestrogen rich food, compared to aromatase inhibitors as a complementary approach to treating estrogen receptor positive breast cancer, as well as the effect of combined flaxseed and aromatase inhibitor therapy on breast cancer treatment. Because of the increasing use of both complementary and alternative approaches to treatment, and the use of aromatase inhibitors in the treatment of breast cancer, the proposed study has potential to provide important clinical information about the effect of foods high in phytoestrogens on a common endocrine therapy used in breast cancer.
Detailed Description
Although the 10 year survival rate for women with early stage breast cancer is very good, distant recurrence is still a serious concern, especially for estrogen receptor positive women. Consequently, breast cancer survivors are interested in therapies that might improve their recurrence free survival (RFS). Used in postmenopausal women, aromatase inhibitors (AI) block the peripheral conversion of androgens to estrogen, effectively lowering the estradiol available to promote breast tumor proliferation. However, use of AIs is associated with hot flashes, joint pain, bone loss, and an increase in cardiac events. Furthermore, many breast tumors eventually develop resistance to hormonal treatments. Complementary and alternative medicines (CAMs) are widely used by cancer survivors in an attempt to reduce disease recurrence with fewer side effects and potential health benefits, and use is particularly prevalent among breast cancer survivors. Flaxseed (FS) is a commonly available food often consumed as a dietary supplement and is the richest food source of lignans, a phytoestrogen. In experimental models, flaxseed consumption has been shown to exhibit a number of activities that suggest a potential benefit of flaxseed in the adjuvant setting. However, the majority of human studies investigating the biologic effects of flaxseed have involved healthy women. There is a paucity of clinical data regarding the efficacy and safety of use of flaxseed among women with breast cancer, especially among those receiving AIs. Because the phytoestrogens in flaxseed can influence many of the same biologic pathways affected by hormonal agents, diet-drug interactions are possible. Additionally, it is possible flaxseed could act through growth and signaling pathways, modifying the development of endocrine resistance. Potential synergistic or antagonistic effects between flaxseed and antiestrogens are of particular interest given the increasing use of AIs to treat postmenopausal women with hormone responsive disease. We propose to conduct a pilot 2x2 factorial randomized intervention study between tumor biopsy and resection, in postmenopausal women diagnosed with ER positive breast cancer, to assess the effects of flaxseed and AI on a number of steroid hormone and tumor-related characteristics associated with long-term survival, and to investigate the potential interaction between flaxseed and AI on tumor expression of Ki-67, caspase, ERα, ERβ, PgR, HER2, IGF1, IGFIR. The pre-surgical setting offers a unique opportunity to rapidly obtain information on intervention related effects on growth factor and signaling pathways related to tumor characteristics in a short time period without the interference of other treatments. We hypothesize that both flaxseed and AI interventions will independently favorably affect growth factor and signaling pathway protein expression resulting in reduced tumor proliferation and increased apoptosis. We further hypothesize that these improvements will be reflected in improved recurrence scores as estimated by the Mammostrat antibody panel (Applied Genomics Incorporated). The proposed study will provide important clinical data for future dietary intervention studies involving phytoestrogen lignans from flaxseed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast neoplasms, phytoestrogens, tumor characteristics, proliferation, apoptosis, estrogen receptor, HER2

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
2
Arm Type
Experimental
Arm Description
Flaxseed 25 mg per day and 1 placebo pill per day
Arm Title
3
Arm Type
Experimental
Arm Description
25 mg flaxseed per day and 1 mg anastrozole pill per day
Arm Title
4
Arm Type
Placebo Comparator
Arm Description
Placebo pill 1 per day
Arm Title
1
Arm Type
Experimental
Arm Description
Anastrozole 1 mg pill per day
Intervention Type
Drug
Intervention Name(s)
Anastrozole
Other Intervention Name(s)
Arimidex
Intervention Description
1 mg per day
Intervention Type
Dietary Supplement
Intervention Name(s)
flaxseed
Intervention Description
25 g per day ground
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo pill 1 per day
Primary Outcome Measure Information:
Title
Expression of Estrogen Receptor (ER-beta)
Description
Mean percentage of cells expressing estrogen receptor (ER-beta)
Time Frame
Biopsy/Week 1 and Surgical Resection/Week 2
Title
Progesterone Receptor (PR) Expression
Description
Mean percentage of cells expressing PR
Time Frame
Biopsy/Week 1 and Surgical Resection/Week 2
Title
Human Epidermal Growth Factor Receptor 2 (Her2) Expression
Description
Mean percentage of cells expressing human epidermal growth factor receptor 2 (Her2)
Time Frame
Biopsy/Week 1 and Surgical Resection/Week 2
Secondary Outcome Measure Information:
Title
Growth Hormone Serum Levels IGF-1
Description
Mean serum level IGF-1(pg/ml)
Time Frame
Biopsy/Week 1 and Surgical Resection/Week 2

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 and ≤ 85 years Postmenopausal status defined as: no menstrual cycle in the past 12 months hysterectomy with bilateral oophorectomy hysterectomy with intact ovaries if age > 55 years Newly diagnosed with incident, primary, invasive, estrogen receptor positive clinical stage II or lower breast cancer ECOG performance status of 1 or less Willingness to comply with study guidelines and procedures Willingness and ability to provide informed consent Usual consumption of soy no more than 1 time per week and willingness to avoid whole soy foods or concentrated soy sources (soy milk, tofu, substitute meat products, meal replacement bars) during the intervention period Willingness to avoid herbal and dietary supplements (not including vitamins), aspirin, and ibuprofen during the intervention period No competing neoadjuvant or chemotherapy treatment Time between pre-surgical visit and surgery must be at least 2 weeks No chemotherapy in the past 12 months Exclusion Criteria: Inability to read and write English Previous invasive breast cancer Insulin dependent Type I or II diabetes diagnosed by physician History of coagulopathy, thrombocytopenia, or bleeding disorder Current (past 30 days) regular (at least once per week) use of reproductive hormone therapy, Tamoxifen, aromatase inhibitors, or other estrogen inhibitors, flaxseed, or antibiotics Current chemotherapy or neoadjuvant chemotherapy Allergies to flaxseed, nuts, or other seeds Renal dysfunction defined as creatinine > 1.5 mg/dl History of Crohns' disease, ulcerative colitis, irritable bowel syndrome, celiac sprue, or other malabsorption syndrome, diverticulitis, diverticulosis, or other bowel diagnosis which, in the opinion of the breast surgeon, would contraindicate large doses of dietary fiber or would impair nutrient absorption Current, regular (more than once weekly) use of prescription blood-thinning agents including coumadin, heparin and heparin related drugs, clopidogrel bisulfate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tracey L O'Connor, MD
Organizational Affiliation
Roswell Park Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Roswell Park Cancer Institute
City
Buffalo
State/Province
New York
ZIP/Postal Code
14263
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24669750
Citation
McCann SE, Edge SB, Hicks DG, Thompson LU, Morrison CD, Fetterly G, Andrews C, Clark K, Wilton J, Kulkarni S. A pilot study comparing the effect of flaxseed, aromatase inhibitor, and the combination on breast tumor biomarkers. Nutr Cancer. 2014;66(4):566-75. doi: 10.1080/01635581.2014.894097. Epub 2014 Mar 26.
Results Reference
derived

Learn more about this trial

Flaxseed, Aromatase Inhibitors and Breast Tumor Characteristics

We'll reach out to this number within 24 hrs