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临床试验/NCT03307460
NCT03307460Unknown2 期

Phase II Trial: uPAR-PET/MR in Patients With Newly Diagnosed Prostate Cancer; Non-invasive Characterization of Tumor Aggressiveness

Rigshospitalet, Denmark1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2017年11月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
52
试验地点
1
主要终点
Correlation with Gleason Score

研究概览

简要总结

Prospective study to evaluate the value of uPAR-targeted PET/MR scan using the tracer 68Ga-NOTA-AE105 in patients with newly diagnosed prostate cancer

详细描述

Prostate cancer is one of the most frequent types of cancer in men. The characteristics of the disease varies significantly among patients where some have an indolent type of cancer, from which they will never experience symptoms while others have highly aggressive malignant disease that requires prompt therapeutic action.

Treatment of localized prostate cancer is based on a risk stratification, where patients are either offered therapy with curative intent - surgery or radiotherapy - or in case of low-risk disease an "active surveillance" strategy can be advised. In active surveillance the disease is monitored by PSA measurement, repeated biopsies and digital rectal examination. Some patients progress during active surveillance to a higher risk classification, which may lead to selection of active therapy.

The aim of this study is to investigate positron emission tomography (PET) with the radiolabelled tracer 68Ga-NOTA-AE105, combined with magnetic resonance imaging (MRI) in patients with newly diagnosed prostate cancer. 68Ga-NOTA-AE105 targets the receptor urokinase-type plasminogen activator receptor (uPAR), which is a known marker for aggressive disease in prostate cancer.

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

  • Histologically verified prostate cancer
  • Capable of understanding written information and giving informed consent
  • Planned to enter active surveillance strategy or undergo therapy with curative intent (surgery or radiotherapy)

排除标准

  • Obesity (Body weight over 140 kg)
  • Known allergy to 68-Ga-NOTA-AE105
  • Metallic components in the body that contradicts MRI scan
  • Severe claustrophobia making the person unable to complete an MRI scan

研究组 & 干预措施

uPAR PET/MRI

Experimental

68Ga-NOTA-AE105 is injected once for performing a PET/MRI scan

干预措施: 68Ga-NOTA-AE105 (Drug)

结局指标

主要结局

Correlation with Gleason Score

时间窗: 3 months after PET/MRI

Correlate the uptake of 68Ga-NOTA-AE105 with Gleason Score obtained from biopsy material.

次要结局

  • Prognostic value(3 years from PET/MRI)
  • Diagnostic accuracy in staging lymph nodes(3 months from PET/MRI)

研究者

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

Marie Øbro Fosbøl

Medical doctor

Rigshospitalet, Denmark

研究点 (1)

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