grant

A novel paradigm of sensitization of the tumor microenvironment with image-guided ultrasound cavitation and mechanotherapeutics for targeted HCC treatment

Organization UNIVERSITY OF WASHINGTONLocation SEATTLE, UNITED STATESPosted 15 Aug 2022Deadline 31 May 2027
NIHUS FederalResearch GrantFY202514-HydroxydaunomycinAblationAbscissionAcademiaAcuteAdriamycineAngiotensin ReceptorAnimalsAnti-Hypertensive AgentsAnti-Hypertensive DrugsAnti-HypertensivesArteriesBAY 54-9085BioavailabilityBiological AvailabilityBiomedical EngineeringBiophysical ProcessBlood VesselsCancer CauseCancer EtiologyCancersCessation of lifeChemoembolizationChemotherapy EmbolizationClinicalClinical ResearchClinical StudyClinical TrialsCollaborationsDeathDevelopmentDiagnosisDisciplineDiseaseDisorderDoseDoxorubicinDoxorubicinaDrug DeliveryDrug Delivery SystemsDrug TargetingDrug TherapyDrugsEffectivenessEligibilityEligibility DeterminationExcisionExtirpationFutureGenetic EngineeringGenetic Engineering BiotechnologyGenetic Engineering Molecular BiologyGoalsHepatocarcinomaHepatocarcinoma modelHepatocellular CarcinomaHepatocellular cancerHepatomaHepatotoxic effectHepatotoxicityHydroxyl DaunorubicinHydroxyldaunorubicinHypotensive AgentHypotensive DrugsIndustryInvestigatorsKO miceKnock-out MiceKnockout MiceLiverLiver Cells CarcinomaLiver ToxicityLosartanMalignant CellMalignant NeoplasmsMalignant TumorMechanicsMediatingMedicationMicrobubblesModelingMonitorNatureNull MouseOncologyOncology CancerOperative ProceduresOperative Surgical ProceduresOutcomePatientsPharmaceutical PreparationsPharmacological TreatmentPharmacotherapyPhysiologic AvailabilityPrimary carcinoma of the liver cellsProceduresPropertyProtocol ScreeningPublic HealthRecombinant DNA TechnologyRemovalResearchResearch PersonnelResearchersResistanceRiskSYS-TXScientistSorafenibSurgicalSurgical InterventionsSurgical ProcedureSurgical RemovalSystemic TherapyTechniquesTestingTherapeuticTherapeutic InterventionTimeToxic effectToxic effect on liver cellsToxicitiesTransplantationTreatment EfficacyTreatment outcomeWorkadvanced diseaseadvanced illnessanti-hypertensionbio-engineeredbio-engineersbioengineeringbiological engineeringbiophysical mechanismcancer cellcancer microenvironmentcancer typechemotherapeutic agentchemotherapeutic compoundschemotherapeutic drugschemotherapeutic medicationschemotherapycurative interventioncurative therapeuticcurative therapycurative treatmentsdevelopmentaldrug interventiondrug treatmentdrug/agentgenetically engineeredhepatic body systemhepatic organ systemhepatic toxicityhepatocellular carcinoma cancer modelhepatocellular carcinoma modelhepatoxicityhuman modelimage guidanceimage guidedimprovedin vivo Modelinnovateinnovationinnovativeinterestintervention efficacyintervention therapyliver cancer modelliver carcinomalozartanmalignancymechanicmechanicalmechanical propertiesmodel of humanmouse modelmurine modelneoplasm/cancernew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapy approachesnew treatment approachnew treatment strategynovelnovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapy approachpharmaceutical interventionpharmacological interventionpharmacological therapypharmacology interventionpharmacology treatmentpharmacotherapeuticspre-clinical efficacypre-clinical studyprecision medicineprecision-based medicinepreclinical efficacypreclinical studypressureresectionresistantresponsesubcutaneoussubdermalsuper high resolutionsuperresolutionsurgerysynergismsystemic toxicitytherapeutic efficacytherapeutic outcometherapy efficacytherapy outcometransplanttumortumor microenvironmentultra high resolutionultrasounduptakevascular
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Full Description

ABSTRACT
The purpose of this project is to develop a novel image-guided approach for modulating the tumor

microenvironment (TME) of HCC with combined mechanotherapeutic drugs (MechTx) and ultrasound cavitation

treatment (USCTx), and evaluate its therapeutic efficacy. We plan to implement USCTx and the targeting and

monitoring of the combined (with MechTx) treatment on a clinical scanner in order to make it widely available for

future preclinical and clinical studies. Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related

deaths worldwide with an estimated 750,000 new cases per year. Most patients with HCC who are not candidates

for surgical removal or ablation are treated with either transarterial chemoembolization or systemic

chemotherapy. Yet these treatments result in only limited improvements in patient survival at the expense of

considerable toxicities. Our main hypothesis is that the combined USCTx and MechTx will lead to tumor

pressure, stiffness and vascular changes that promote increased local tumor uptake of systemic or transarterial

chemotherapeutics, and will result in better therapy outcomes. While the discovery of new chemotherapeutic

agents and interventional procedures will continue to evolve, our approach to modulate the TME with combined

MechTx and USCTx aims to dramatically improve chemotherapy outcomes with both the existing and future

chemotherapy agents. A strong interdisciplinary team (bioengineers, scientists, clinicians) from academia and

industry will collaborate in the following aims: (Aim 1) Evaluate the ability of MechTx to modulate the tumor

microenvironment and enhance drug delivery; (Aim 2) Evaluate the ability of USCTx to modulate the tumor

microenvironment and enhance drug delivery; (Aim 3) Evaluate the ability of combined MechTx and USCTx to

modulate the tumor microenvironment and enhance drug delivery; and (Aim 4) Demonstrate the preclinical

efficacy of chemotherapeutics when combined with MechTx and USCTx in survival studies using two in vivo

models of HCC. The innovation of the project is in: (a) the use of MechTx as a novel therapeutic strategy to

modulate tumor pressure, microvascular flow, and stiffness of the TME; (b) implementing image-guided USCTx

on a clinical ultrasound scanner leading to translatable precision medicine for HCC; (c) utilizing the synergy of

MechTx and USCTx as a novel and innovative approach for modulating the TME to maximize chemotherapy

outcomes; and (d) combining super resolution and nonlinear Doppler processing to spatially and temporarily

super-resolve the vasculature of tumors undergoing treatments that target the TME. The proposed project will

take advantage of the distinct, yet synergistic mechanisms of MechTx and USCTx as a novel paradigm of

sensitization of the TME to chemotherapeutics, leading to better treatment outcomes and overall survival for

HCC patients initially and patients of other malignancies and diseases in the future.

Grant Number: 5R01EB032655-04
NIH Institute/Center: NIH

Principal Investigator: MICHALAKIS AVERKIOU

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