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Completed

NCT Number: NCT00042731

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

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.

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Key information

Age range

45 year–80 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

CCOP - Western Regional, Arizona, Phoenix, Arizona, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

lycopene

Dietary Supplement

Daily administration as outlined in treatment arm(s)

Multivitamin

Dietary Supplement

Daily administration as outlined in treatment arm(s)

Soy isoflavones

Dietary Supplement

Daily administration as outlined in treatment arm(s)

Primary outcomes

  1. Occurrences of Treatment Effect on Biomarkers in Each Group

    Time frame: 4 years

    Effect 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 outcomes

  1. Occurrences of Plasma Level Changes for Each Group

    Time frame: 4 years

    Plasma levels of isoflavones and lycopene as measured by plasma analysis at baseline and post-study intervention

  2. Occurrence of Tissue Level Increases

    Time frame: 4 years

    Correlation of plasma and tissue levels of isoflavones and lycopene as measured by plasma and tissue analysis at baseline and post-study intervention

  3. Occurrences of Disease Progression for Each Group

    Time frame: 4 years

    Effect of isoflavones and lycopene on markers of disease progression as measured by prostate-specific antigen (PSA) levels at baseline and post-study intervention

  4. Occurrences of Hormonal Effect

    Time frame: 4 years

    Effect 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

Sponsors and collaborators

Lead sponsor

H. Lee Moffitt Cancer Center and Research Institute

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

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

Important dates

Study start
2002
Primary completion
2006
Study completion
2006
First posted
Jan 27, 2003
Registry last updated
Sep 24, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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