A Study Using 18F-FAZA and PET Scans to Study Hypoxia in Pancreatic Cancer

Pancreatic Cancer Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01542177
• Other study ID #: FAZA-Pancreas
• Status: Completed
• Start date: February 2012
• Est. completion date: September 2019

Study information

• Verified date: May 2022
• Source: University Health Network, Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: September 2019
• Est. primary completion date: September 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 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 2.
• 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)

Exclusion Criteria:

• 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

Related Conditions & MeSH terms

• Hypoxia
• Pancreatic Cancer
• Pancreatic Neoplasms

Locations

Country	Name	City	State
Canada	Princess Margaret Hospital	Toronto	Ontario

Sponsors (2)

Lead Sponsor	Collaborator
University Health Network, Toronto	Canadian Cancer Society (CCS)

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Measure the hypoxia level in Patients with Pancreatic Cancer using Positron Emission Tomography (PET) with 18F-Fluoroazomycin Arabinoside (18F-FAZA).		2 years
Secondary	Correlate FAZA PET uptake in pancreatic cancer with the extension of the disease.	Standardized uptake statistics will be calculated for each volume of interest (VOI): Maximum standardized uptake value (SUVMax), mean standardized uptake value (SUVMean) and standard deviation of standardized uptake values (SUVSD).	2 years
Secondary	Correlate FAZA PET uptake in pancreatic cancer with CA 19-9 levels.	Standardized uptake statistics will be calculated for each volume of interest (VOI): Maximum standardized uptake value (SUVMax), mean standardized uptake value (SUVMean) and standard deviation of standardized uptake values (SUVSD). These parameters will be correlated with increasing or decreasing CA 19-9 levels (U/ml).	2 years
Secondary	Correlate FAZA PET uptake in pancreatic cancer with tumor response.	Standardized uptake statistics will be calculated for each volume of interest (VOI): Maximum standardized uptake value (SUVMax), mean standardized uptake value (SUVMean) and standard deviation of standardized uptake values (SUVSD). Tumor response is measured in millimeters. Complete response is a tumor reduction of <5 mm, partial response is at least a 30% reduction, progressive disease is a 20% increase, and stable disease is no increase in shrinkage and no increase in growth.	2 years
Secondary	Correlate FAZA PET uptake in pancreatic cancer with patient disease-free survival (DFS).	Kaplan-Meier actuarial method and/or the Cox proportional hazard model will be utilized.	2 years
Secondary	Compare the pattern of FAZA uptake in different tumor sites (eg., lymph node metastases and liver metastasis).	Standardized uptake statistics will be calculated for each volume of interest (VOI): Maximum standardized uptake value (SUVMax), mean standardized uptake value (SUVMean) and standard deviation of standardized uptake values (SUVSD).	2 years
Secondary	Determine the feasibility of using dynamic and static PET imaging of FAZA uptake in patients with pancreatic cancer.		2 years