grant

A Computational Framework Enabling Virtual Imaging Trials of 3D Quantitative Optoacoustic Tomography Breast Imaging

Organization UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGNLocation CHAMPAIGN, UNITED STATESPosted 1 Aug 2022Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY20253-D3-Dimensional3DAccelerationAcousticsAnatomic SitesAnatomic structuresAnatomyBloodBlood Reticuloendothelial SystemBody TissuesBreastBreast CancerBreast MRIBreast Magnetic Resonance ImagingBreast TissueBreast UltrasonographyCAT scanCT X RayCT XrayCT imagingCT scanCancersClinicClinicalClinical TrialsCommunitiesComputational toolkitComputed TomographyComputer ModelsComputerized ModelsComputing MethodologiesConsumptionCoupledDataDetectionDevelopmentEthicsFutureGenerationsGoalsHemoglobinHumanHypoxiaHypoxicImageIntermediary MetabolismInvestigatorsIonizing Electromagnetic RadiationIonizing radiationKnowledgeLesionLightMalignant Breast NeoplasmMalignant NeoplasmsMalignant TumorMammary Gland ParenchymaMammary Gland TissueMammary UltrasonographyMammogramMammographyMeasurementMeasuresMetabolicMetabolic ProcessesMetabolismMethodsModalityModelingModern ManO elementO2 elementOpticsOxygenOxygen DeficiencyPathologicPhotoradiationPhysicsPhysiologicPhysiologicalPlayProbabilityProcessPropertyRadiation-Ionizing TotalResearchResearch PersonnelResearchersResolutionRoentgen RaysRoleSystemTechniquesTechnologyTimeTissue imagingTissuesTomodensitometryTranslatingTranslationsUltrasonic MammographyUltrasound MammographyX-RadiationX-Ray CAT ScanX-Ray Computed TomographyX-Ray Computerized TomographyX-Ray RadiationX-rayXrayXray CAT scanXray Computed TomographyXray computerized tomographyaccurate diagnosisangiogenesisbreast cancer diagnosisbreast imagingbreast ultrasoundcancer imagingcancer progressioncatscanclinical developmentclinical imagingcomputational frameworkcomputational methodologycomputational methodscomputational modelingcomputational modelscomputational toolboxcomputational toolscomputational toolsetcomputed axial tomographycomputer based methodcomputer based modelscomputer frameworkcomputer methodscomputer tomographycomputerized axial tomographycomputerized modelingcomputerized tomographycomputerized toolscomputing methodcostcost efficientdata acquisitiondata acquisitionsdensitydesigndesigningdevelopmentaldiffuse optical tomographyethicalexperimentexperimental researchexperimental studyexperimentsimage constructionimage generationimage reconstructionimage-based methodimagerimagingimaging methodimaging modalityimaging studyin silicointerestionizing outputmalignancymalignant breast tumormammary imagingmammographic Imagingmammographic examinationsmammographic examsneoplasm progressionneoplasm/cancerneoplastic progressionnon-contrast CTnon-invasive imagingnoncontrast CTnoncontrast computed tomographynoninvasive imagingnoveloncologic imagingoncology imagingopen sourceopticaloptoacoustic tomographyphotoacoustic tomographypublic health relevancequantitative imagingreconstructionresolutionssimulationsocial rolethree dimensionaltooltranslationtumortumor growthtumor imagingtumor progressionvirtual imaging
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Full Description

ABSTRACT
Optoacoustic tomography (OAT), also known as photoacoustic computed tomography, is a non-invasive

imaging modality actively being developed for breast cancer imaging and other biomedical applications. A

unique feature of OAT is the ability to produce an image based on the endogenous optical contrast associated

with the concentration and oxygenation state of hemoglobin within tissue, without ionizing radiation and without

the loss of spatial resolution typically associated with purely optical techniques such as optical diffusion

tomography. Because aggressively growing malignant breast tumors tend to be under hypoxia and decreased

blood oxygen saturation due to substantially increased metabolic activity in comparison to healthy tissue, an

optimized and validated OAT system can be a powerful tool for the management of breast cancer by assessing

density of the tumor microvasculature and its blood oxygenation.

Currently, there is no validated OAT method that is sufficiently accurate for widespread clinical imaging of

the breast; important issues such as optimal hardware and image reconstruction designs, the ability to resolve

lesions at depth, and quantitative imaging remain unresolved. Due to the competing requirements of light

delivery and acoustic detection, a variety of different system designs for breast OAT have been proposed; this

is unlike in x-ray mammography, breast MRI and breast ultrasound, where very similar implementations are in

use per modality. Considering the large number of parameters involved, it is infeasible to systematically

optimize breast OAT through human trials due to time- and cost-constraints and ethical concerns. However,

virtual imaging trials (VITs), where an imaging study is conducted in silico by use of representative numerical

phantoms and imaging models, can offer a rapid and cost-efficient means of assessing and optimizing new

imaging concepts and technologies such as OAT. The ability to conduct VITs for 3D OAT is currently lacking.

The broad objective of this project is to develop, validate, and demonstrate computational tools for

performing VITs that can inform the development of clinically viable and effective 3D breast OAT technologies.

This will afford researchers an unprecedented level of control in modeling and validating quantitative OAT

imaging of the tumor and tissue oxygen saturation distributions necessary for assessing breast cancer. The

results will be the first of their kind evaluating the task-based merits and capabilities of OAT and the knowledge

attainable in these studies is critical for translating this technology to the clinic.

The Specific Aims of the project are: Aim 1. To develop multi-physics simulation tools for the in silico

simulation of realistic measurement data in 3D breast OAT; Aim 2. To systematically develop and refine

quantitative OAT image reconstruction methods; Aim 3. To conduct physical experiments that will be used to

validate the computational models; Aim 4. To conduct VITs to explore quantitative OAT system optimization.

Grant Number: 5R01EB031585-04
NIH Institute/Center: NIH

Principal Investigator: Mark Anastasio

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