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Selenium and Prostate Cancer: Clinical Trial on Availability to Prostate Tissue and Effects on Gene Expression (SePros)

Primary Purpose

Prostatic Neoplasms, Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Selenium
Sponsored by
Wageningen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prostatic Neoplasms focused on measuring Prostate Cancer, Selenium, Chemoprevention, Gene expression

Eligibility Criteria

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

Inclusion Criteria:

  • male
  • biopsy proven prostate cancer
  • scheduled for radical prostatectomy

Exclusion Criteria:

  • liver diseases (e.g. hepatitis)
  • kidney diseases
  • inflammatory bowel diseases
  • use of dietary supplements containing selenium
  • adjuvant therapy for prostate cancer (e.g. hormonal therapy, HIFU)
  • previously or concurrent diagnosed with cancer, other than prostate cancer

Sites / Locations

  • University Medical Centre St Radboud
  • Wageningen University

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Selenium (selenized yeast)

Arm Description

Placebo

Selenium (selenized yeast) tablets, 300 ug/day

Outcomes

Primary Outcome Measures

selenium levels in prostate tissue
changes in gene expression profiles in prostate tissue

Secondary Outcome Measures

changes in blood flow, vessel permeability and exocrine functionality
changes in gene expression profiles in blood cells

Full Information

First Posted
March 12, 2007
Last Updated
March 11, 2011
Sponsor
Wageningen University
Collaborators
World Cancer Research Fund International
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1. Study Identification

Unique Protocol Identification Number
NCT00446901
Brief Title
Selenium and Prostate Cancer: Clinical Trial on Availability to Prostate Tissue and Effects on Gene Expression
Acronym
SePros
Official Title
Selenium and Prostate Cancer: Clinical Trial on Availability to Prostate Tissue and Effects on Gene Expression
Study Type
Interventional

2. Study Status

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

3. Sponsor/Collaborators

Name of the Sponsor
Wageningen University
Collaborators
World Cancer Research Fund International

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to determine whether selenium supplementation leads to changes in selenium levels and gene expression profiles in prostate tissue.
Detailed Description
Rationale: Prostate cancer is a frequently observed malignancy in men, especially in elderly men. Besides diagnosis and treatment, also prevention of prostate cancer is an important point of interest to reduce the incidence and mortality of prostate cancer. Selenium is considered to be a promising chemopreventive agent for prostate cancer. Exact mechanisms of chemoprevention by selenium are not fully understood. However, it is expected that selenium (among other effects) directly affects gene expression in the prostate. Objective: The aim of this study is to get insight into bioavailability of selenium in prostate tissue and changes of gene expression profiles that might be responsible for selenium-induced chemoprevention. To meet this objective, the relationship between dietary selenium intake and changes in gene expression profiles, tissue selenium levels and blood flow in prostate tissue will be examined. Study design: The present study is designed as a double-blind, randomized and placebo-controlled intervention trial. Blood samples, toenails, questionnaires, MR images and surgical specimens will be collected to examine effects of selenium supplementation. Study population: The study population will consist of 60 men, diagnosed with prostate cancer and scheduled for radical prostatectomy. Written informed consent will be obtained from each participant. Intervention: Participants will receive 300 ug selenium / day or a placebo during 5 weeks prior to radical prostatectomy. Selenium will be supplemented in the form of selenized yeast tablets (SelenoPrecise, Pharma Nord). Main study parameters: Levels of selenium in prostate tissue and changes in prostate gene expression profiles of participants supplemented with selenium or placebo, compared before and after the short intervention period, will be considered as the main parameters of the present study. Besides gene expression profiles in prostate tissue, also gene expression profiles of peripheral mononuclear cells (PBMC), levels of selenium in blood and toenails and blood flow and permeability of blood vessels of prostate tissue will be analyzed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms, Prostate Cancer
Keywords
Prostate Cancer, Selenium, Chemoprevention, Gene expression

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Arm Title
Selenium (selenized yeast)
Arm Type
Experimental
Arm Description
Selenium (selenized yeast) tablets, 300 ug/day
Intervention Type
Dietary Supplement
Intervention Name(s)
Selenium
Other Intervention Name(s)
SelenoPrecise, PharmaNord
Intervention Description
Selenized yeast, 300 ug/day
Primary Outcome Measure Information:
Title
selenium levels in prostate tissue
Time Frame
after 5 weeks of intervention with selenium or placebo
Title
changes in gene expression profiles in prostate tissue
Time Frame
after 5 weeks of intervention with selenium or placebo
Secondary Outcome Measure Information:
Title
changes in blood flow, vessel permeability and exocrine functionality
Time Frame
after 5 weeks of intervention with selenium or placebo
Title
changes in gene expression profiles in blood cells
Time Frame
after 5 weeks of intervention with selenium or placebo

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: male biopsy proven prostate cancer scheduled for radical prostatectomy Exclusion Criteria: liver diseases (e.g. hepatitis) kidney diseases inflammatory bowel diseases use of dietary supplements containing selenium adjuvant therapy for prostate cancer (e.g. hormonal therapy, HIFU) previously or concurrent diagnosed with cancer, other than prostate cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
J.A. Witjes, Md PhD Prof
Organizational Affiliation
University Medical Center St Radboud
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
L.A.L.M. Kiemeney, PhD Prof
Organizational Affiliation
University Medical Center St Radboud
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
P. van 't Veer, PhD Prof
Organizational Affiliation
Wageningen University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
L.A. Afman, PhD
Organizational Affiliation
Wageningen University
Official's Role
Study Chair
Facility Information:
Facility Name
University Medical Centre St Radboud
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6500 HB
Country
Netherlands
Facility Name
Wageningen University
City
Wageningen
State/Province
Gelderland
ZIP/Postal Code
6700 EV
Country
Netherlands

12. IPD Sharing Statement

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Selenium and Prostate Cancer: Clinical Trial on Availability to Prostate Tissue and Effects on Gene Expression

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