grant

Scintillation Photon Counting Detectors for 100 ps Time-of-Flight PET Imaging

Organization UNIVERSITY OF CALIF-LAWRENC BERKELEY LABLocation BERKELEY, UNITED STATESPosted 30 Sept 2022Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY20253-D3-Dimensional3DAddressAreaBiteCell Communication and SignalingCell SignalingClinicalCollectionCommunitiesCoupledDataDetectionDevelopment and ResearchDoseElectronicsElementsEventFrequenciesFutureGoalsHot SpotImageImage EnhancementImaging PhantomsIntracellular Communication and SignalingLesionLightMeasurementNoiseOpticsPETPET ScanPET imagingPETSCANPETTPathway interactionsPatientsPerformancePhotonsPhotoradiationPhysiologic pulsePositionPositioning AttributePositron Emission Tomography Medical ImagingPositron Emission Tomography ScanPositron-Emission TomographyPulseR & DR&DRad.-PETRadiation DoseRadiation Dose UnitRecoveryResolutionRoleScanningSignal TransductionSignal Transduction SystemsSignalingStarvationStreamSystemTechniquesTechnologyTimeTracerTranslatingVariantVariationVisualizationWidthWorkadvanced systemanalogattenuationbiological signal transductionclinical imagingcomputerized data processingcostdata processingdesigndesigningdetectorelectronicelectronic deviceimage constructionimage generationimage reconstructionimagingimaging capabilitiesimaging studyimprovedinstrumentationmulti-photonnovelopticalpathwayphoton detectionphoton-counting detectorpositron emission tomographic (PET) imagingpositron emission tomographic imagingpositron emitting tomographypreservationprototyperesearch and developmentresolutionsresponsesingle photon detectorsocial rolespatial and temporalspatial temporalspatiotemporalthree dimensionaltomographyuptake
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Full Description

Project Summary
Clinical time-of-flight positron emission tomography (TOF-PET) systems capable of excellent coincidence time

resolution (CTR) promise to drastically enhance effective 511 keV photon sensitivity. The ability to more precisely

localize annihilation origins along system response lines constrains event data, providing improved signal-to-

noise ratio (SNR) and reconstructed image quality by associating 511 keV photons more closely to their true

origin. This SNR enhancement increases as CTR is improved, and a major goal of ongoing PET instrumentation

research and development is to push system CTR ≤100 ps full-width-at-half-maximum (FWHM). At this level of

performance, events are constrained ≤1.5 cm, providing more than a five-fold increase in SNR relative to a

system with no TOF capability. Advanced systems capable of ≤100 ps FWHM CTR would effectively more than

double or quadruple the effective 511 keV system sensitivity, in comparison to state-of-the-art, clinical TOF-PET

systems (250-400 ps FWHM CTR). Thus, advancing CTR is also a pathway for greatly improved system

sensitivity without increasing detection volume and system cost. Standard PET detectors comprising segmented

arrays of high-aspect-ratio scintillation crystal elements cannot achieve this level of performance and are

ultimately limited by poor light collection efficiency and depth-dependent scintillation photon transit time jitter

seen by the photodetector. To address this, we propose to develop a new detector readout concept which allows

scintillation photons to be counted and a unique timestamp to be assigned for the first arriving photon at each

photosensor pixel. We will leverage this new advancement in scalable PET detector readout and produce PET

detector modules capable of high resolution, three-dimensional positioning capabilities and 100 ps FWHM CTR

in a design that also makes no sacrifices on 511 keV photon detection efficiency. The new detector design will

be integrated into large area detector modules that span the full axial extent (>20 cm) of a clinical PET system,

including front-end signal and back-end data processing. We will construct a prototype tomographic imaging

setup and quantify relevant system performance metrics and the imaging performance of future clinical systems

made from this new detector. The proposed PET detector technologies can have a significant impact on

quantitative PET imaging. The image SNR enabled by the significant boost in effective sensitivity can be

employed to substantially reduce tracer dose and shorten scan time/increase patient throughput, or to better

visualize and quantify smaller lesions/features in the presence of significant background, which are important

features that can make PET more practical and accurate, as well as help to expand its roles in patient

management.

Grant Number: 5R01EB033402-04
NIH Institute/Center: NIH

Principal Investigator: Joshua Cates

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