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临床试验/NCT02391025
NCT02391025已完成早期 1 期

Gallium-68 Citrate PET To Detect MYC Amplification in Metastatic Castrate Resistant Prostate Cancer

Rahul Aggarwal1 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2015年5月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
39
试验地点
1
主要终点
Mean maximum Standardized Uptake Value (SUVmax)

研究概览

简要总结

This is a single center, pilot, cross-sectional imaging study investigating the use of gallium-68 citrate PET in participants with metastatic castration-resistant prostate cancer who are planning to undergo a metastatic tumor biopsy on protocol NCT02432001 (CC#125519).

The study population will consist of participants with metastatic castration-resistant prostate cancer who are undergoing a metastatic tumor biopsy as part of clinical protocol NCT02432001 (CC#125519), with evidence of resistance to androgen signaling inhibition.

详细描述

Primary Objective:

I. To determine the association between maximum average of standard uptake value (SUVmax-ave) of target metastatic lesions on gallium-68 citrate PET with MYC amplification determined from analysis of circulating tumor DNA.

Secondary Objectives:

I. To determine the accuracy rate, sensitivity, specificity of gallium citrate PET in the detection of metastatic lesions as compared to standard staging scans including cross-sectional imaging of the abdomen/pelvis and whole body bone scan.

II. To determine the optimal dose of gallium-68 citrate and timing of scan post-injection to maximize tumor-to-background signal.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Male participants with histologically confirmed prostate cancer
  • Participants must have castrate levels of testosterone (< 50 ng/dL) on Luteinizing hormone-releasing hormone (LHRH) analogue or have had prior bilateral orchiectomy, with evidence of castration-resistant disease by Prostate Cancer Clinical Trials Working Group 2 (PCWG2) criteria
  • Age 18 years or older at the time of study entry
  • Minimum of at least three discrete metastatic lesions in the bone and/or soft tissue amenable to whole body Positron Emission Tomography (PET) imaging per the judgment of study radiologist
  • For participants who undergo optional metastatic tumor biopsy following completion of gallium citrate PET:
  • Presence of one or more metastases by standard radiographic scans that is safely accessible to tumor biopsy in the judgment of treating clinician and/or Interventional Radiology

排除标准

  • Contra-indications to MRI, including permanent pacemaker, implantable device, aneurysm clip, or severe claustrophobia (for participants planning to be imaged on PET/ Magnetic resonance imaging(MRI) scanner)
  • Active infection within 14 days of study enrollment
  • For participants who undergo optional metastatic tumor biopsy following completion of gallium citrate PET:
  • History of radiation therapy to the target metastatic lesion selected for tumor biopsy
  • Contra-indication to biopsy including uncontrolled bleeding diathesis.
  • Platelets >75,000/μl and prothrombin time (PT) or international normalized ratio (INR) and a partial prothrombin time (PTT) < 1.5 times the institutional upper limit of normal (ULN) within 14 days prior to biopsy.

研究组 & 干预措施

Gallium-68 citrate, PET

Experimental

Participants will receive a single scan obtained on a single day, followed by optional tumor biopsy within 6 weeks of scan. There will be optional follow up gallium-68 citrate PET scan to assess response to treatment received outside this study that will be completed within 12 weeks of baseline scan.

干预措施: Gallium-68 citrate (Drug)

Gallium-68 citrate, PET

Experimental

Participants will receive a single scan obtained on a single day, followed by optional tumor biopsy within 6 weeks of scan. There will be optional follow up gallium-68 citrate PET scan to assess response to treatment received outside this study that will be completed within 12 weeks of baseline scan.

干预措施: Positron Emission Tomography (PET) (Procedure)

结局指标

主要结局

Mean maximum Standardized Uptake Value (SUVmax)

时间窗: Day of imaging (1 day)

The mean and standard deviation of SUVmax of gallium-68 citrate (across all metastatic lesions per participant) will be reported.

Mean maximum Standardized Uptake Value (SUVmax-ave)

时间窗: Day of imaging (1 day)

The mean and standard deviation of SUVmax-ave of gallium-68 citrate across all participants in the study cohort will be descriptively reported.

次要结局

  • Correlation between SUVmax and MYC gene expression(Day of imaging (1 day))
  • Correlation between SUVmax and transferrin receptor gene expression(Day of imaging (1 day))
  • Mean SUVmax-ave percent change from baseline(Up to 12 weeks)
  • Sensitivity of gallium-68 PET(Day of imaging (1 day))
  • Specificity of gallium-68 PET(Day of imaging (1 day))
  • Positive predictive value (PPV) of gallium-68 PET(Day of imaging (1 day))
  • Number of participants with reported treatment-emergent adverse events(Up to 12 weeks)

研究者

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

Rahul Aggarwal

Assistant Clinical Professor

University of California, San Francisco

研究点 (1)

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