跳至主要内容
临床试验/NCT02783950
NCT02783950进行中(未招募)不适用

Genomics in Michigan Impacting Observation or Radiation (G-MINOR)

University of Michigan Rogel Cancer Center26 个研究点 分布在 1 个国家目标入组 356 人开始时间: 2017年1月17日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
356
试验地点
26
主要终点
Number of Participants That Receive Adjuvant Therapy (Radiation and/or Hormone Therapy)

研究概览

简要总结

To determine the impact of Decipher test results on adjuvant treatment decisions of high-risk post-RP patients with undetectable post-op prostate specific antigen (PSA) compared to clinical factors alone.

详细描述

This prospective, randomized trial will compare the receipt of adjuvant therapy for high-risk radical prostatectomy (RP) patients who undergo Decipher testing to those who do not. 350 subjects from within the statewide Michigan Urological Surgery Improvement Collaborative (MUSIC) will be randomized to either a Genomic Classifier (Decipher) or Usual-Care-Based (UC) strategy for a period of three months. If enrolled during the Genomic Classifier period, both subjects and their treating physician will be provided Decipher results and CAPRA-S scores. In the UC periods, CAPRA-S scores but not Decipher results will be provided.

The enrollment goal, initially and throughout the study, was to enroll 350 evaluable patients. During the study, the target accrual goal was raised to 550 patients to allow more flexibility among sites to achieve the enrollment goal of 350 evaluable patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

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

  • Prostate cancer patients who have undergone radical prostatectomy
  • PSA < 0.1 ng/ml at enrollment
  • At least one of the following:
  • pT3 (seminal vesicle invasion or extraprostatic extension), or
  • Positive surgical margins
  • Radical prostatectomy within one year of enrollment

排除标准

  • Individuals who have any of the following will not be eligible to participate:
  • Have regional or distant metastatic disease
  • Received any radiation or hormone therapy (neo-adjuvant, adjuvant, or salvage)
  • Node positive

结局指标

主要结局

Number of Participants That Receive Adjuvant Therapy (Radiation and/or Hormone Therapy)

时间窗: within 18 months of radical prostatectomy

Adjuvant will be defined as preceding biochemical recurrence (BCR) (i.e.: PSA ≥ 0.2 ng/ml) and within 18 months of radical prostatectomy.

次要结局

  • Michigan Urological Surgery Improvement Collaborative (MUSIC) Patient Reported Outcomes (PRO)(Up to 24 months post radical prostatectomy)
  • Time (From Randomization) to Adjuvant Treatment Administration(Up to 18 months post randomization)
  • Time (From Randomization) to Salvage Treatment Administration(Up to 5 years post randomization)
  • Time (From Randomization) to Biochemical Recurrence (BCR)(Up to 5 years post randomization)
  • Time (From Randomization) to Metastatic Disease (Regional or Distant)(Up to 5 years post randomization)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (26)

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