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Vitamin D Effects on Prostate Pathology (DProstate)

Primary Purpose

Prostate Cancer

Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
vitamin D3 (cholecalciferol)
Sponsored by
University of Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring vitamin D, prostate cancer, prostatectomy, pathology, immunohistochemistry

Eligibility Criteria

30 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of a Gleason score 6 or 7 adenocarcinoma of the prostate biopsy
  • Patient has elected to have a radical prostatectomy
  • Patient is determined fit for surgery
  • Normal renal and hepatic function
  • Normal serum and urine calcium values
  • Normal serum phosphate values
  • Normal serum parathyroid hormone values
  • Signed written informed consent

Exclusion Criteria:

  • Prior use of neoadjuvant androgen deprivation therapy
  • Prior use of 5 alpha reductase inhibitors (finasteride or dutasteride) in last 12 months
  • Previous or concomitant anti-cancer therapy (chemotherapy, radiotherapy)
  • Gleason score 8-10 adenocarcinoma as a biopsy diagnosis
  • History of hypercalcemia/hypercalciuria
  • History of renal disease
  • History of sarcoidosis
  • Vitamin D (cholecalciferol) supplement > 1000 IU/day
  • Inability to comply with a study protocol

Sites / Locations

  • University Health Network

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

1

2

3

Arm Description

vitamin D3 (400 IU/d)

vitamin D3 (10,000 IU/d)

vitamin D3 (40,000 IU/d)

Outcomes

Primary Outcome Measures

immunohistochemical markers of prostate pathology
intraprostate vitamin D metabolites

Secondary Outcome Measures

calcium (serum and urine)
parathyroid hormone (PTH)
prostate specific antigen (PSA)
creatinine (serum and urine)
phosphate (serum)
serum vitamin D metabolites

Full Information

First Posted
August 25, 2008
Last Updated
September 29, 2011
Sponsor
University of Toronto
Collaborators
Mount Sinai Hospital, Canada, University Health Network, Toronto, Sunnybrook Health Sciences Centre, Canadian Cancer Society (CCS)
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1. Study Identification

Unique Protocol Identification Number
NCT00741364
Brief Title
Vitamin D Effects on Prostate Pathology
Acronym
DProstate
Official Title
Randomized Trial of the Effects of Vitamin D on Prostate Cancer-associated Lesions and on Vitamin D Metabolites in Prostate
Study Type
Interventional

2. Study Status

Record Verification Date
September 2011
Overall Recruitment Status
Unknown status
Study Start Date
September 2008 (undefined)
Primary Completion Date
February 2012 (Anticipated)
Study Completion Date
July 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Toronto
Collaborators
Mount Sinai Hospital, Canada, University Health Network, Toronto, Sunnybrook Health Sciences Centre, Canadian Cancer Society (CCS)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
There is much interest in understanding the role that vitamin D3 (cholecalciferol) plays in various cancers, and in the prognosis of various cancers once they are discovered. The purpose of this study is to examine the effects of vitamin D on prostate cancer-associated lesions and on vitamin D metabolites in prostate tissue. We will give vitamin D3 to men when they are scheduled to have their prostate removed because of cancer. The men will take vitamin D at one of 3 doses for 4-6 weeks, until the surgery is performed. We will compare the prostate tissue taken from the men receiving the higher doses of vitamin D to tissue from men assigned to the lower doses. We expect to find that the prostate removed at surgery from men who received the high-dose vitamin D treatment will appear more normal, and less cancer like. In addition, we will measure vitamin D metabolites in the prostate to confirm that these did accumulate in the prostate to bring about the effects observed.
Detailed Description
Epidemiologic, laboratory, and clinical reports all suggest that vitamin D3 (cholecalciferol) plays a desirable role in the prevention and prognosis of prostate and other cancers. Prostate cancer cells possess both of the enzymes required to convert vitamin D to the active paracrine hormone, calcitriol. However, the dose-response relationship between serum levels of calcidiol (vitamin D status) and prostate tissue levels of calcidiol and calcitriol is yet to be defined. As a neoadjuvant, prior to radical prostatectomy (for 4-6 wk) vitamin D3 [400 IU (control group), 10,000 IU or 40,000 IU/day] will be given to 90 men randomized, double-blinded, 30 per dose. Immediately after surgery, the pathologist will obtain a few grams of prostate tissue, some of which will be used to assay calcidiol and calcitriol within prostate. From the embedded prostate, we will prepare immunohistochemically stained sections to characterize cellular responses and morphological changes. Our hypothesis is that vitamin D will increase intraprostate calcitriol concentration and thereby lower cellular proliferation (as judged by the markers MIB-1 and p27) in zones of Gleason pattern 3 prostate cancer and in pre-cancerous (PIN) lesions. We expect that our results will provide surrogate outcomes to justify larger trials of vitamin D for treatment of prostate cancer. This research has the potential to: 1. Provide direct evidence at the cellular level using clinical samples that vitamin D lowers cellular proliferation in prostate cancer, 2. Provide guidance about the serum calcidiol concentrations (and thereby vitamin D doses) that should be targeted for such studies, and 3. Eventually support other research directed at vitamin D as a primary prevention strategy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
vitamin D, prostate cancer, prostatectomy, pathology, immunohistochemistry

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
vitamin D3 (400 IU/d)
Arm Title
2
Arm Type
Active Comparator
Arm Description
vitamin D3 (10,000 IU/d)
Arm Title
3
Arm Type
Active Comparator
Arm Description
vitamin D3 (40,000 IU/d)
Intervention Type
Dietary Supplement
Intervention Name(s)
vitamin D3 (cholecalciferol)
Intervention Description
liquid vitamin D solution (vitamin D3 in ethanol) taken daily at one of three possible doses (400, 10000, or 40000 IU/d) for 4-6 weeks prior to radical prostatectomy
Primary Outcome Measure Information:
Title
immunohistochemical markers of prostate pathology
Time Frame
end-of-study
Title
intraprostate vitamin D metabolites
Time Frame
end-of-study
Secondary Outcome Measure Information:
Title
calcium (serum and urine)
Time Frame
biweekly
Title
parathyroid hormone (PTH)
Time Frame
baseline, final
Title
prostate specific antigen (PSA)
Time Frame
baseline, final
Title
creatinine (serum and urine)
Time Frame
biweekly
Title
phosphate (serum)
Time Frame
biweekly
Title
serum vitamin D metabolites
Time Frame
baseline, final

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of a Gleason score 6 or 7 adenocarcinoma of the prostate biopsy Patient has elected to have a radical prostatectomy Patient is determined fit for surgery Normal renal and hepatic function Normal serum and urine calcium values Normal serum phosphate values Normal serum parathyroid hormone values Signed written informed consent Exclusion Criteria: Prior use of neoadjuvant androgen deprivation therapy Prior use of 5 alpha reductase inhibitors (finasteride or dutasteride) in last 12 months Previous or concomitant anti-cancer therapy (chemotherapy, radiotherapy) Gleason score 8-10 adenocarcinoma as a biopsy diagnosis History of hypercalcemia/hypercalciuria History of renal disease History of sarcoidosis Vitamin D (cholecalciferol) supplement > 1000 IU/day Inability to comply with a study protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reinhold Vieth, PhD
Organizational Affiliation
University of Toronto, Mount Sinai Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dennis Wagner, MSc
Organizational Affiliation
University of Toronto, Mount Sinai Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Theo van der Kwast, MD, PhD, FRCPC
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Neil Fleshner, MD, MPH, FRCSC
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Laurence Klotz, MD, FRCSC
Organizational Affiliation
Sunnybrook Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada

12. IPD Sharing Statement

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Vitamin D Effects on Prostate Pathology

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