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临床试验/NCT00953225
NCT00953225已完成2 期

Vitamin D Supplementation in Veterans With Early-Stage Prostate Cancer

VA Office of Research and Development2 个研究点 分布在 1 个国家目标入组 83 人开始时间: 2010年1月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
83
试验地点
2
主要终点
PSA Slope (Trajectory) or the Change in PSA Level Over Time

研究概览

简要总结

Vitamin D promotes the differentiation of prostate cancer cells, maintains the differentiated phenotype of prostate epithelial cells, and can induce prostate cancer cell death, raising the possibility that vitamin D deficiency over time promotes the progression of subclinical prostate cancer to clinical disease. The investigators propose to conduct a clinical study aimed at measuring the efficacy of vitamin D3 (4000IU/day) supplementation in Veterans diagnosed with low-risk, early-stage prostate cancer, who elect to have their disease monitored through active surveillance. The successful completion of this proposed clinical study will allow us to determine whether correcting vitamin D deficiency in Veterans diagnosed with early-stage prostate cancer will prevent progression of their disease and improve their prognosis.

详细描述

Vitamin D promotes the differentiation of prostate cancer (PCa) cells, maintains the differentiated phenotype of prostate epithelial cells, and can induce prostate cancer cell death, raising the possibility that vitamin D deficiency over time promotes the progression of subclinical PCa to clinical disease. These considerations support the use of vitamin D3 as a chemopreventive agent.

We hypothesize that a daily dose of vitamin D3 (4,000 IU) taken for one year by Veterans diagnosed with low-risk, early-stage PCa, who are eligible for active surveillance will: a) result in a measurable decrease of serum PSA levels in a significant number of enrolled subjects, and b) be associated with a stabilization or improvement of their PCa pathology, as assessed through histological examination of prostate tissue biopsy specimens (Gleason score and percent of positive biopsies) obtained at the end of the study, as part of their standard medical care for active surveillance.

This VA Merit application proposes to conduct a randomized, placebo-controlled clinical study aimed at measuring the efficacy of vitamin D3 (4000IU/day) supplementation in Veterans diagnosed with early-stage prostate cancer, who elect to have their disease monitored through active surveillance (before considering definitive therapy). The main objectives of this proposed clinical study are as follows:

  1. To determine whether a daily supplement of 4,000 IU of vitamin D3 taken for twelve months will result in a measurable and significant decrease of serum PSA levels in Veterans diagnosed with low-risk, early stage PCa (Gleason score 6, PSA 10, clinical stage T1C or T2a), who elect to have their disease monitored through active surveillance for at least one year.
  2. To determine in enrolled Veterans the pathology status of their PCa by analyzing prostate tissue biopsy specimens at the end of the study (Gleason score and percentage of positive biopsies), and by comparing them with those obtained before enrollment in this study, as part of their standard medical care.

The implementation of these proposed studies will allow us to assess whether vitamin D3 supplementation can be utilized as a chemopreventive regimen in Veterans diagnosed with low-risk, early stage PCa, and provide a useful addition to active surveillance.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
19 Years 至 85 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Male Veterans (> 18 years of age) recently diagnosed with low-risk PCa (histologically documented adenocarcinoma of the prostate)
  • A serum PSA value of up to 10.0 ng/ml, and a Gleason score of six or less (three or less in either architectural pattern)
  • For the purpose of eligibility, these additional criteria will be verified: *serum creatinine 2.0 mg/dL
  • serum phosphate (measured as phosphorus) > 2.3 and < 4.8 mg/dL
  • serum calcium > 8.5 and < 10.5 mg/dL

排除标准

  • Subjects with any concurrent malignancy, except non-melanoma skin cancer
  • Subjects with a history of sarcoidosis
  • Subjects with a history of high-dose (1,000 IU per day) vitamin D supplementation
  • Subjects with a history of hypercalcemia
  • Subjects who use lithium as a medication

研究组 & 干预措施

Vitamin D3

Experimental

4,000 IU vitamin D3 daily for one year

干预措施: vitamin D3 (Drug)

Placebo

Placebo Comparator

Placebo daily for one year

干预措施: Placebo daily for one year (Drug)

结局指标

主要结局

PSA Slope (Trajectory) or the Change in PSA Level Over Time

时间窗: 1 year (visits # 1-8)

Change in PSA (ng/mL) from baseline to 1 year visit, which include the baseline through 1 year follow-up.

次要结局

  • Number of Positive Biopsy Cores (Out of Twelve) Compared to the Corresponding Values Assessed Before Enrollment(1 year)

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (2)

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