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临床试验/NCT00668642
NCT00668642已完成2 期

Effect of Dutasteride on Androgen-Response Gene Expression During the Tumor Regrowth Phase of Intermittent Androgen Ablation Therapy in Patients With Advanced Prostate Cancer

NorthShore University HealthSystem3 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2007年3月最近更新:
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
20
试验地点
3
主要终点
Relative Expression of U19 Gene in Tumor From Prostate Gland During First Off-cycle.

研究概览

简要总结

The purpose of this study is to determine if the drug dutasteride increases expression of genes that slow the growth of prostate cancer during treatment with intermittent androgen ablation therapy (hormone therapy).

详细描述

We have shown in a murine model of treatment with intermittent androgen ablation therapy of prostate cancer that when dutasteride is given during the regrowth phase (off-phase) of intermittent therapy, that tumor growth is inhibited and that survival is improved. We have also shown that testosterone is a more potent inducer of certain tumor suppressor androgen response genes than dihydrotestosterone. In this murine model, we showed that use of a 5-alpha reductase inhibitor (dutasteride) resulted in significant hyperinduction of the U19 tumor suppressor androgen response gene during the regrowth phase of treatment. In the current clinical trial, we will determine if use of dutasteride in men with advanced prostate cancer during the off-phase of intermittent androgen ablation therapy will also result in hyperinduction of these tumor suppressor androgen response genes. Gene expression will be measured in tumor tissue obtained by prostate biopsies during the off-phase when the testosterone level has normalized. Prostate-specific antigen (PSA) levels will also be measured to determine the PSA doubling time during the off-phase to determine the effect of dutasteride on PSA kinetics.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • Histologically proven prostate cancer
  • Patients are hormone-naive
  • Patients either to begin androgen ablation therapy with luteinizing hormone-releasing hormone (LHRH) agonist or already receiving therapy with LHRH agonist
  • Advanced prostate cancer with either positive pelvic nodes or bone/visceral metastasis
  • Must have an intact prostate (no previous surgery or XRT)
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-2
  • Recovery from any major infection or surgical procedure
  • Signed informed consent

排除标准

  • Known intolerance or allergy to dutasteride
  • Concomitant chemotherapy, biologic therapy, or XRT to prostate
  • Bilateral orchiectomy
  • Prior malignancy within 5 years of registration

研究组 & 干预措施

A: Dutasteride During First Off-Cycle

Experimental

Arm A patients received dutasteride (0.5 mg/day) during the first off-cycle and received placebo during the second off-cycle

干预措施: Dutasteride (Drug)

B: Placebo During First Off-Cycle

Placebo Comparator

Arm B patients received placebo during the first off-cycle and received dutasteride (0.5 mg/day) during the second off-cycle

干预措施: Placebo (Drug)

结局指标

主要结局

Relative Expression of U19 Gene in Tumor From Prostate Gland During First Off-cycle.

时间窗: At the end of off-cycle 1 defined by when the testosterone level reaches normal (approximately 6 months)

Calculation of the level of gene expression of the U19 tumor suppressor gene compared between the 2 arms at the end of "off-treatment" cycle 1.

次要结局

  • Determination of Prostate-specific Antigen (PSA) Doubling Time During First Off-cycle(At month 9 and ongoing monthly until end of off-cycle 1 defined by when the testosterone level reaches normal (approximately 6 months))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel Shevrin

Principal Investigator, Division of Hematology/Oncology

NorthShore University HealthSystem

研究点 (3)

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