Prostate Cancer Clinical Trial

Low-Fat Diet and/or Flaxseed in Preventing Prostate Cancer

Summary

RATIONALE: A diet that is low in fat and/or high in flaxseed may slow or prevent disease progression of prostate cancer.

PURPOSE: Randomized phase II trial to study the effectiveness of a diet that is low in fat and/or high in flaxseed in slowing or preventing disease progression in patients who have newly diagnosed prostate cancer.

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Full Description

OBJECTIVES:

Compare tumor proliferation in patients with newly diagnosed prostate cancer eating fat- and/or flaxseed-modified diets.
Compare differences in histopathological markers associated with prostate cancer (rates of apoptosis, extent of high-grade prostatic intraepithelial neoplasia) among patients in these diet groups.
Compare changes in serum prostate specific antigen among patients in these diet groups.
Compare changes in hormone-related factors (total serum testosterone and free androgen index, insulin-like growth factor [IGF], and IGF-binding protein-3) among patients in these diet groups.
Compare the effects of diet on nutritional biomarkers (levels of lignans in the urine and ejaculate, fatty acid profiles of erythrocytes and prostatic tissue) in these patients.
Determine associations between dietary modification and changes in dietary biomarkers, hormonal intermediates, and study endpoints in these patients.

OUTLINE: This is a randomized study. Patients are stratified according to Gleason score (less than 7 vs at least 7) and race (black vs non-black). Patients are randomized to 1 of 4 diet groups.

Arm I (Flaxseed-supplemented diet): Patients are instructed to incorporate ground flaxseed into their daily diets.
Arm II (Low-fat diet): Patients are instructed on ways to achieve a diet with no greater than 20% of total energy from dietary fat.
Arm III (Flaxseed-supplemented, low-fat diet): Patients are instructed as in arm I and arm II.
Arm IV (Control diet): Patients are contacted weekly, but do not receive dietary counseling until after surgery.

All patients ingest the diets for at least 3 weeks and complete diet diaries until surgery. After surgery, all patients receive dietary counseling.

PROJECTED ACCRUAL: A total of 160 patients (40 per treatment arm) will be accrued for this study.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Histologically confirmed prostate cancer
At least 3 weeks until planned prostatectomy (24 days between day 1 visit and surgery)
Current diet that provides more than 30% of calories from fat

PATIENT CHARACTERISTICS:

Age

18 and over

Performance status

Not specified

Life expectancy

Not specified

Hematopoietic

Not specified

Hepatic

Not specified

Renal

Not specified

Other

Mentally competent
Able to speak and write English
Must have telephone access

PRIOR CONCURRENT THERAPY:

Biologic therapy

Not specified

Chemotherapy

Not specified

Endocrine therapy

No concurrent hormonal therapy

Radiotherapy

Not specified

Surgery

At least 2 weeks since prior prostate biopsy

Other

At least 7 days since prior antibiotics
No prior therapy for prostate cancer
No concurrent dietary supplements initiated within the past 3 months or anticipated to begin during study except standard multivitamin/mineral preparations (e.g., One-A-Day, Theragran, or Centrum) that do not supply > 100% of the recommended daily allowance of any vitamin or mineral
No other concurrent neoadjuvant therapies
No other concurrent flaxseed consumption

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

161

Study ID:

NCT00049309

Recruitment Status:

Completed

Sponsor:

Duke University

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There are 3 Locations for this study

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University of Michigan Comprehensive Cancer Center
Ann Arbor Michigan, 48109, United States
Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill
Chapel Hill North Carolina, 27599, United States
Duke Comprehensive Cancer Center
Durham North Carolina, 27710, United States

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

161

Study ID:

NCT00049309

Recruitment Status:

Completed

Sponsor:


Duke University

How clear is this clinincal trial information?

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