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临床试验/NCT01542177
NCT01542177已完成不适用

The Evaluation of Hypoxia Imaging in Patients With Pancreatic Cancer Using Positron Emission Tomography (PET) With 18F-Fluoroazomycin Arabinoside (18F-FAZA)

University Health Network, Toronto1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2012年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
48
试验地点
1
主要终点
Measure the hypoxia level in Patients with Pancreatic Cancer using Positron Emission Tomography (PET) with 18F-Fluoroazomycin Arabinoside (18F-FAZA).

研究概览

简要总结

This is a diagnostic study to look for low levels of oxygen (hypoxia) in pancreatic cancer using an imaging test called positron emission tomography (PET). Hypoxia can influence how pancreatic cancer grows and responds to treatments such as chemotherapy and radiotherapy. The use of PET scans to measure hypoxia may be better and simpler than the approaches used previously. This study will assess whether or not PET scans using a tracer called 18F-FAZA (18F-Fluoroazomycin Arabinoside) can provide useful information about hypoxia in pancreatic cancer. Also as part of the study, a blood sample will be taken to study biomarkers (substances in the body that may be important indicators of hypoxia and/or pancreatic cancer) that may be useful in studying pancreatic cancer and hypoxia.

详细描述

This is a single centre, single arm hypoxia study of pancreatic cancer with PET FAZA imaging.

PET-CT imaging of tumor hypoxia with FAZA will be done prior to the start of standard treatment for pancreatic cancer with chemotherapy. The FAZA PET-CT imaging session will last approximately 2.5 hours and include an initial dynamic scan to completely characterize the initial rapid phase of FAZA uptake, followed by a later static scan.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • •Minimum age of 18 years old
  • •Histologic diagnosis of pancreatic adenocarcinoma
  • •TNM (7th edition) cT1-4, N0-1, M0-1
  • •No cytotoxic anti-cancer therapy for advanced / metastatic pancreatic cancer prior to study entry
  • •Ability to provide written informed consent to participate in the study
  • •ECOG performance status 0, 1 or
  • •Patient should have the following blood counts at baseline: ANC equal or greater to 1.5 x 109/L; Platelets equal or greater to 100 x 109/L; Hgb equal or greater to 9g/Dl
  • •Patient should have the following blood chemistry levels at baseline: AST (SGOT), ALT (SGPT) equal or less than 5 x upper limit of normal range (ULN) is allowed
  • •Patient has an identifiable tumor (pancreatic tumor and/or metastasis) by imaging (CT scan and/or MR)
  • •Patient must agree to use contraception considered adequate and appropriate by the investigator and if the patient is female of child-bearing potential, as evidenced by regular menstrual periods, she must have a negative serum pregnancy test (B-hCG)

排除标准

  • •Inability to lie supine for more than 30 minutes
  • •Any other type of primary cancer
  • •Life expectancy of less than 12 weeks
  • •Patient has known brain metastases unless previously treated and well controlled for at least 3 months (defined as stable clinically, no edema, no steroids and stable in two scans at least 4 weeks apart)
  • •Patient has serious medical risk factors involving any of the major organ systems

研究组 & 干预措施

Pancreatic cancer

结局指标

主要结局

Measure the hypoxia level in Patients with Pancreatic Cancer using Positron Emission Tomography (PET) with 18F-Fluoroazomycin Arabinoside (18F-FAZA).

时间窗: 2 years

次要结局

  • Determine the feasibility of using dynamic and static PET imaging of FAZA uptake in patients with pancreatic cancer.(2 years)
  • Correlate FAZA PET uptake in pancreatic cancer with CA 19-9 levels.(2 years)
  • Compare the pattern of FAZA uptake in different tumor sites (eg., lymph node metastases and liver metastasis).(2 years)
  • Correlate FAZA PET uptake in pancreatic cancer with the extension of the disease.(2 years)
  • Correlate FAZA PET uptake in pancreatic cancer with tumor response.(2 years)
  • Correlate FAZA PET uptake in pancreatic cancer with patient disease-free survival (DFS).(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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