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Isoflavones & Lycopene in Localized Prostate Ca:Prior to Radical Prostatectomy

A Randomized Pilot Clinical Trial Of The Action Of Isoflavones And Lycopene In Localized Prostate Cancer: Administration Prior To Radical Prostatectomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00042731
Enrollment
79
Registered
2003-01-27
Start date
2002-07-31
Completion date
2006-08-31
Last updated
2012-09-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

stage I prostate cancer, stage IIB prostate cancer, stage IIA prostate cancer

Brief summary

RATIONALE: Eating a diet rich in isoflavones, compounds found in soy foods, or lycopene, a substance found in tomatoes, may keep prostate cancer from growing. Giving isoflavones or lycopene before surgery may be an effective treatment for prostate cancer. PURPOSE: Randomized clinical trial to compare the effectiveness of isoflavones with that of lycopene before surgery in treating patients who have stage I or stage II prostate cancer.

Detailed description

OBJECTIVES: * Compare the effect of isoflavones vs lycopene prior to radical prostatectomy on intermediate biomarkers (e.g., indices of cell proliferation and apoptosis) in patients with localized prostate cancer. * Compare the effects of these nutritional supplements on increases in plasma levels and tissue levels of these agents in these patients. * Compare the effects of these nutritional supplements on changes in surrogate markers of disease progression (e.g., prostate-specific antigen levels) in these patients. * Compare the effects of these nutritional supplements on changes in serum steroid hormones, estradiol, and free testosterone in these patients. * Compare the magnitude of these changes in patients treated with these nutritional supplements vs patients in the control group. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to disease stage (stage I vs stage II) and presence of high-grade prostatic intraepithelial neoplasia. Patients are randomized to 1 of 7 treatment groups. PROJECTED ACCRUAL: A total of 87 patients will be accrued for this study within 1 year.

Interventions

DIETARY_SUPPLEMENTLycopene

Daily administration as outlined in treatment arm(s)

DIETARY_SUPPLEMENTMultivitamin

Daily administration as outlined in treatment arm(s)

DIETARY_SUPPLEMENTSoy isoflavones

Daily administration as outlined in treatment arm(s)

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
H. Lee Moffitt Cancer Center and Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
45 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed localized prostate cancer * Stage I or II * Scheduled prostatectomy between 4-6 weeks after initial biopsy PATIENT CHARACTERISTICS: Age: * 45 to 80 Performance status: * Not specified Life expectancy: * Not specified Hematopoietic: * Not specified Hepatic: * No known history of hepatic disease Renal: * No known history of renal disease Other: * No known history of thyroid disease * Body mass index no greater than 32 * Omnivorous diet * No known allergy to study supplements * No evidence of prostatitis or urinary tract infection * No other prior malignancy except nonmelanoma skin cancer * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: * Not specified Chemotherapy: * Not specified Endocrine therapy: * No concurrent thyroid hormone replacement medications Radiotherapy: * Not specified Surgery: * See Disease Characteristics Other: * At least 30 days since prior antibiotics * At least 30 days since prior diet high in soy and/or lycopene products (e.g., greater than 40 mg soy/day and/or greater than 15 mg lycopene/day) * No other concurrent nutritional supplements, including modular supplements with other carotenoids and isoflavones * No prior or concurrent therapy for prostate cancer

Design outcomes

Primary

MeasureTime frameDescription
Occurrences of Treatment Effect on Biomarkers in Each Group4 yearsEffect of isoflavones and lycopene on endpoint biomarkers as measured by tissue cell proliferation, apoptosis, or programmed cell death at prostate cancer biopsy and surgical excision

Secondary

MeasureTime frameDescription
Occurrences of Plasma Level Changes for Each Group4 yearsPlasma levels of isoflavones and lycopene as measured by plasma analysis at baseline and post-study intervention
Occurrence of Tissue Level Increases4 yearsCorrelation of plasma and tissue levels of isoflavones and lycopene as measured by plasma and tissue analysis at baseline and post-study intervention
Occurrences of Disease Progression for Each Group4 yearsEffect of isoflavones and lycopene on markers of disease progression as measured by prostate-specific antigen (PSA) levels at baseline and post-study intervention
Occurrences of Hormonal Effect4 yearsEffect of isoflavones and lycopene on serum steroid hormones as measured by sex-hormone-binding globulin, estradiol, and free testosterone at baseline and post-study intervention

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026