Deep Learning Reconstruction for Improved TOF PET Using Histo-Image Partitioning
Project Number5R01EB031806-04
Contact PI/Project LeaderMATEJ, SAMUEL
Awardee OrganizationUNIVERSITY OF PENNSYLVANIA
Description
Abstract Text
Project Summary
Clinical and research applications of the PET imaging are rapidly expanding from ever improving diagnostic
and treatment assessment applications to guidance of personalized treatments, ultra-low dose imaging, and
even interventional imaging procedures. Supporting these developments, reconstruction tools that are able to
reliably handle both typical and (ultra-)low count situations, imperfect data, and data from specialized imaging
geometries, with fast (near real-time) reconstruction performance are of crucial importance. The overall goal of
this project is to develop and investigate robust and efficacious Deep Learning (DL) reconstruction approaches
addressing these needs. A unique and innovative feature of the proposed approaches (compared to alternative
DL applications) is the utilization of list-mode data histogrammed into a very efficient histo-image format. TOF
data partitioned into the histo-image format are characterized by strong local properties, thus perfectly fitting
convolutional neural network formalism and making DL training and reconstruction directly from realistic clinical
data (in size and character) highly feasible and practical.
The clinical utility of PET systems has significantly improved over the years thanks to advances in
instrumentation, data corrections, and reconstruction approaches. Nevertheless, full utilization of their potential
through robust and fast quantitative reconstruction remains a challenge especially for the cases of very low count
data, such as in low-count temporal (motion and dynamic) frames, delayed studies, longitudinal low-dose
studies, and studies using new isotopes with long half-life and low positron fraction rates (e.g. in 89Zr-labeled
CAR-T cell imaging), as well as in specialized PET systems with partial angular coverage, for which exact,
artifact-free, reconstruction does not exist. These are the situations for which the developed DL approaches
promise great potential due to the demonstrated success of the DL networks to be trained for imperfect and very
low count data without reliance on accurate data models. Furthermore, pre-trained networks can provide ultra-
fast, near real-time, performance in practical use.
Specific Aim 1 will develop tools for DL PET reconstruction using histo-image partitioning along with
procedures for training of the proposed DL approaches, including novel approaches advancing the state-of-the-
art of DL reconstruction directly from acquired PET data. Specific Aim 2 is directed towards study and evaluation
of the performance of the investigated DL approaches for whole-body and long axial FOV scanner data for the
wide range of counts from applications such as typical FDG, low dose, delayed, low activity isotope scans, and
ultra-short frames in motion correction and dynamic studies. Specific Aim 3 will develop and apply motion
correction protocols involving the proposed DL reconstruction tools and test and study their efficacy for clinically
realistic situations involving non-rigid lung and heart motions. And finally, Specific Aim 4 is dedicated to an
application and study of the developed DL approaches to specialized PET systems with partial angular coverage.
1
Public Health Relevance Statement
Project Narrative
The major goal of this project is to improve the diagnostic, treatment guidance, and research utility of
quantitative positron emission tomography (PET) imaging, through the development of robust, near real-time,
deep-learning based reconstruction approaches allowing efficacious use of standard, low dose, and novel low
activity imaging molecular bio-tracers. The proposed work is relevant to public health, since an improvement in
the reconstructed images will lead to more accurate diagnosis of diseases and more accurate treatment
guidance and monitoring of the response to therapy, while allowing for decreased patient radiation dose. It will
also facilitate quantitatively reliable tools for research investigations with new radiotracers for PET tailored to
specific diseases.
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National Institute of Biomedical Imaging and Bioengineering
CFDA Code
286
DUNS Number
042250712
UEI
GM1XX56LEP58
Project Start Date
01-July-2021
Project End Date
31-March-2026
Budget Start Date
01-April-2024
Budget End Date
31-March-2026
Project Funding Information for 2024
Total Funding
$586,495
Direct Costs
$360,920
Indirect Costs
$225,575
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Biomedical Imaging and Bioengineering
$586,495
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01EB031806-04
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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News and More
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History
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