search
Back to results

Lycopene in Treating Patients With Prostate Cancer or Benign Prostatic Hyperplasia

Primary Purpose

Nonmalignant Neoplasm, Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
lycopene
laboratory biomarker analysis
biopsy
Sponsored by
University of Illinois at Chicago
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonmalignant Neoplasm focused on measuring benign prostatic hyperplasia, stage I prostate cancer, stage IIB prostate cancer, stage IIA prostate cancer, stage III prostate cancer, stage IV prostate cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

DISEASE CHARACTERISTICS:

  • Diagnosis of 1 of the following:

    • Prostate cancer
    • Benign prostate hyperplasia
  • High blood levels of prostate-specific antigen
  • Enlarged prostate

PATIENT CHARACTERISTICS:

  • Not specified

PRIOR CONCURRENT THERAPY:

  • Not specified

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Ability of prostatic tissue to accumulate doses of lycopene
    Responsiveness of steady state level of DNA oxidation in blood and prostate tissue to lycopene dosing
    Effect of lycopene on lipid peroxidation marker malondialdehyde in serum
    Importance of measuring multiple DNA oxidation products as biomarkers of oxidative stress and its chemoprevention
    Significance of DNA oxidation products in blood as an indicator of oxidative stress in the prostate
    Prostate and blood uptake of the chemoprevention agent lycopene

    Secondary Outcome Measures

    Full Information

    First Posted
    December 27, 2006
    Last Updated
    September 19, 2013
    Sponsor
    University of Illinois at Chicago
    Collaborators
    National Cancer Institute (NCI)
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT00416390
    Brief Title
    Lycopene in Treating Patients With Prostate Cancer or Benign Prostatic Hyperplasia
    Official Title
    The Effect of Lycopene on DNA Damage in Human Prostate
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2007
    Overall Recruitment Status
    Completed
    Study Start Date
    undefined (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    March 2011 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    University of Illinois at Chicago
    Collaborators
    National Cancer Institute (NCI)

    4. Oversight

    5. Study Description

    Brief Summary
    RATIONALE: Chemoprevention is the use of certain substances to keep cancer from forming, growing, or coming back. Eating a diet high in lycopene, a substance found in tomatoes and tomato products, may keep cancer from forming or growing. Collecting and storing samples of blood from patients with cancer to study in the laboratory may help doctors learn more about changes that may occur in DNA and identify biomarkers related to cancer. PURPOSE: This randomized clinical trial is studying how well lycopene works in treating patients with prostate cancer or benign prostatic hyperplasia.
    Detailed Description
    OBJECTIVES: Assess the ability of prostatic tissue to accumulate doses of lycopene in patients with prostate cancer or benign prostate hyperplasia. Determine whether the steady state level of DNA oxidation in blood and prostate tissue is responsive to lycopene dosing. Investigate the effect of lycopene dosing on the lipid peroxidation marker malondialdehyde in serum. Assess the importance of measuring multiple DNA oxidation products as biomarkers of oxidative stress and its chemoprevention. Determine the significance of DNA oxidation products in blood as an indicator of oxidative stress in the prostate. Measure prostate and blood uptake of the chemoprevention agent lycopene. OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive oral lycopene once daily for 3 weeks. Arm II: Patients receive oral placebo once daily for 3 weeks. In both arms, patients undergo biopsy to confirm diagnosis of prostate cancer or benign prostatic hyperplasia after 3 weeks of study therapy. Blood samples are collected at baseline and before surgery for biomarker/laboratory studies. PROJECTED ACCRUAL: A total of 120 patients will be accrued for this study.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Nonmalignant Neoplasm, Prostate Cancer
    Keywords
    benign prostatic hyperplasia, stage I prostate cancer, stage IIB prostate cancer, stage IIA prostate cancer, stage III prostate cancer, stage IV prostate cancer

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    lycopene
    Intervention Type
    Other
    Intervention Name(s)
    laboratory biomarker analysis
    Intervention Type
    Procedure
    Intervention Name(s)
    biopsy
    Primary Outcome Measure Information:
    Title
    Ability of prostatic tissue to accumulate doses of lycopene
    Title
    Responsiveness of steady state level of DNA oxidation in blood and prostate tissue to lycopene dosing
    Title
    Effect of lycopene on lipid peroxidation marker malondialdehyde in serum
    Title
    Importance of measuring multiple DNA oxidation products as biomarkers of oxidative stress and its chemoprevention
    Title
    Significance of DNA oxidation products in blood as an indicator of oxidative stress in the prostate
    Title
    Prostate and blood uptake of the chemoprevention agent lycopene

    10. Eligibility

    Sex
    Male
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    DISEASE CHARACTERISTICS: Diagnosis of 1 of the following: Prostate cancer Benign prostate hyperplasia High blood levels of prostate-specific antigen Enlarged prostate PATIENT CHARACTERISTICS: Not specified PRIOR CONCURRENT THERAPY: Not specified
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Richard B. van Breemen, PhD
    Organizational Affiliation
    University of Illinois at Chicago
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    21430075
    Citation
    van Breemen RB, Sharifi R, Viana M, Pajkovic N, Zhu D, Yuan L, Yang Y, Bowen PE, Stacewicz-Sapuntzakis M. Antioxidant effects of lycopene in African American men with prostate cancer or benign prostate hyperplasia: a randomized, controlled trial. Cancer Prev Res (Phila). 2011 May;4(5):711-8. doi: 10.1158/1940-6207.CAPR-10-0288. Epub 2011 Mar 23.
    Results Reference
    derived

    Learn more about this trial

    Lycopene in Treating Patients With Prostate Cancer or Benign Prostatic Hyperplasia

    We'll reach out to this number within 24 hrs