Green Tea Extract in Treating Patients With Prostate Cancer Undergoing Surgery to Remove the Prostate
This study is currently recruiting patients.
Verified by National Cancer Institute (NCI) April 2007
| Sponsors and Collaborators: |
University of Arizona
|
| Information provided by: |
National Cancer Institute (NCI) |
| ClinicalTrials.gov Identifier: |
NCT00459407 |
|
Purpose
RATIONALE: Green tea extract contains ingredients that may prevent or slow the growth of prostate cancer.
PURPOSE: This phase I trial is studying how well green tea extract works in treating patients with prostate cancer undergoing surgery to remove the prostate.
| Condition |
Intervention |
Phase |
Prostate Cancer
|
Drug: green tea extract
Procedure: biological markers
Procedure: biologically based therapies
Procedure: biopsies
Procedure: cancer prevention intervention
Procedure: complementary and alternative therapy
Procedure: conventional surgery
Procedure: diagnostic test
Procedure: herbal medicine / botanical therapy
Procedure: high performance liquid chromatography
Procedure: immunoenzyme techniques
Procedure: immunohistochemistry
Procedure: mass spectrometry
Procedure: neoadjuvant therapy
Procedure: nutritional supplementation
Procedure: surgery
|
Phase I
|
MedlinePlus
related topics:
Prostate Cancer
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control
Official Title: Phase Ib Study of Polyphenon E in a Pre-Prostatectomy Prostate Cancer Cohort
Further study details as provided by National Cancer Institute (NCI):
Primary Outcome Measures:
-
Post-treatment green tea catechin concentration levels in prostate tissue
Secondary Outcome Measures:
-
Clusterin, matrix metalloproteinase (MMP)-2, and MMP-9 levels
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Serum levels of insulin-like growth factor (IGF)-1 and IGF binding protein-3
-
Ratio of 8OHdG:dG
Total Enrollment: 50
Study start: January 2006
OBJECTIVES:
Primary
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Determine the bioavailability of green tea catechins in prostate tissue after treatment with defined green tea extract in patients with prostate cancer.
Secondary
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Determine the effect of this treatment on changes in clusterin levels and matrix metalloproteinase (MMP)-2 and MMP-9 in prostate tissue from these patients.
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Determine the effect of this treatment on changes in serum insulin-like growth factor (IGF)-1 and IGF binding protein-3 in these patients.
-
Determine the effect of this treatment on changes in oxidative DNA damage in peripheral blood leukocytes in these patients.
OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are randomized to 1 of 2 treatment arms.
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Arm I: Patients receive oral green tea extract daily for 4-7 weeks.
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Arm II: Patients receive oral placebo daily for 4-7 weeks. All patients undergo surgery one day after the last dose of study agent. Biopsies are taken at the time of surgery. Plasma and tissue catechin levels are measured with high performance liquid chromatography (HPLC). 8OHdG levels in peripheral blood are measured with HPLC and mass spectometry. Immunohistochemistry is used to measure matrix metalloproteinase (MMP)-2, MMP-9, and clusterin. Insulin-like growth factor (IGF)-1 and IGF binding protein-3 are measured with immunoenzyme techniques.
PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Male
Criteria
DISEASE CHARACTERISTICS:
PATIENT CHARACTERISTICS:
PRIOR CONCURRENT THERAPY:
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No prior therapy for prostate cancer (i.e., hormone therapy, radiation therapy, or surgery)
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No systemic treatment (chemotherapy) and/or radiation therapy for any malignancy within the past 5 years (excluding nonmelanoma skin cancer or cancer confined to organs with surgical removal as the only treatment)
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No regular tea consumption (> 6 servings of hot tea or 12 servings of iced tea or equivalent combination per week) within the past month
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No other concurrent investigational agents
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No other concurrent consumption of tea or tea-derived products from green, black, or oolong tea
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00459407
United States, Arizona
Arizona Cancer Center at University of Arizona Health Sciences Center, Tucson, Arizona, 85724-5024, United States; Recruiting
Clinical Trials Office - Arizona Cancer Center 520-626-9008
United States, Maryland
NIH - Warren Grant Magnuson Clinical Center, Bethesda, Maryland, 20892-1182, United States; Recruiting
Patient Recruitment 800-411-1222
Study chairs or principal investigators
Frederick R. Ahmann, MD, Study Chair, University of Arizona
More Information
Clinical trial summary from the National Cancer Institute's PDQ® database
Study ID Numbers: CDR0000538554; UARIZ-UAZ05-6-01; UARIZ-BIO-06-132
Last Updated: April 25, 2007
Record first received: April 9, 2007
ClinicalTrials.gov Identifier:
NCT00459407