Pocket Phantom Tool in Improving Accuracy of Quantitative PET/CT Imaging of Patients With Solid Tumors



Status:Recruiting
Healthy:No
Age Range:21 - Any
Updated:11/14/2018
Start Date:August 24, 2016
End Date:August 2019

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Calibrated Methods for Quantitative PET/CT Imaging Phase II

This pilot study tests the pocket phantom tool in improving the accuracy of quantitative
positron emission tomography/computed tomography (PET/CT) imaging of patients with solid
tumors. The pocket phantom tool may help test the accuracy of the PET/CT scanner and indicate
whether adjustments need to be made to get consistent information.

PRIMARY OBJECTIVES:

I. Optimize the pocket phantom source design and the bias estimation algorithm: determine the
tolerances and variations in the source sphere geometry and radioactive filing process;
evaluate the need for higher-activity sources in the presence of increased attenuation (i.e.
thicker patients); optimize CT contrast levels for source boundary detection and localization
from CT images; evaluate the robustness for use with different scanner parameters (e.g. CT
slice thicknesses); modify bias estimation algorithm as needed to take into account changes.

II. Develop automated and robust ID pocket phantom processing and web-based software as a
service (SAS) analysis tools: automate initial identification of approximate location of the
pocket phantom; add automated DICOM analysis for web-based SAS analysis tools for imaging
sites.

III. Conduct phantom studies at multiple imaging centers to evaluate the performance with
different imaging protocols, scanners, and reconstruction methods. Also test at multiple time
points over 6-9 months to assess longitudinal stability.

IV. Conduct a comparative study with patients (at University of Washington [UW]) at multiple
time points over 6-12 months to evaluate the performance of the pocket phantom in oncology
patient imaging compared with current clinical practice.

OUTLINE:

Patients undergo a PET/CT scan as part of their standard clinical care. While still
positioned for the clinical scan, patients undergo additional research PET/CT scans in a
smaller region over 10 minutes with the pocket phantom placed nearby and a low-dose single
bed position CT scan for attenuation correction (CTAC).

Inclusion Criteria:

- Patient receiving clinically indicated PET/CT scan

- Patient has a known solid tumor

- Patient provides consent

- Patient can tolerate additional time in scanner (i.e. not claustrophobic)

Exclusion Criteria:

- Patient is pregnant

- Patient cannot or does not provide consent
We found this trial at
1
site
Seattle, Washington 98109
Principal Investigator: Paul Kinahan
Phone: 206-543-0236
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from
Seattle, WA
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