grant

Deploying Histotripsy Based Tumor Ablation Strategies to Treat Pancreatic Cancer

Organization VIRGINIA POLYTECHNIC INST AND ST UNIVLocation BLACKSBURG, UNITED STATESPosted 1 May 2022Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2026AblationAcousticsAfter CareAfter-TreatmentAftercareAnatomic SitesAnatomic structuresAnatomyAnimal ModelAnimal Models and Related StudiesAntitumor ResponseBlood VesselsBody TissuesCancer cell lineCancersCessation of lifeChemotherapy and RadiationChemotherapy and/or radiationClinicalClinical TrialsComplicationDataDeathDevelopmentDiagnosisDiameterDiseaseDisorderDoseDuctDuct (organ) structureElectroporationFamily suidaeFeedbackFocused Ultrasound AblationFocused Ultrasound TherapyFocused Ultrasound TreatmentFutureHigh Power Focused UltrasoundHigh-intensity focused ultrasoundHumanImmune responseImmunocompetentImmunocompromisedImmunocompromised HostImmunocompromised PatientImmunosuppressed HostIn SituInjuryIntestinalIntestinesLocationMalignant NeoplasmsMalignant Pancreatic NeoplasmMalignant TumorMalignant neoplasm of pancreasMechanicsMethodsMiceMice MammalsModalityModelingModern ManMurineMusNodulePDX modelPancreasPancreas CancerPancreas NeoplasmsPancreas TumorPancreaticPancreatic CancerPancreatic TumorPancreatic ductPancreatitisPathological ConstrictionPatient derived xenograftPatientsPhysiologicPhysiologicalPigsPre-Clinical ModelPreclinical ModelsPrognosisPulse PressureRecurrenceRecurrentResearchRiskRuptureSafetyShapesSiteStenosisStructureSuidaeSurvival RateSwineTechniquesTestingTherapeuticTimeTissuesTransducersTreatment ProtocolsTreatment RegimenTreatment ScheduleUnited StatesUnresectableWirsung canalWorkanti-tumor immune responseanti-tumor responsebile ductbile ductulebowelcancer progressionchemo/radiation therapychemotherapy and radiotherapyclinical relevanceclinical translationclinically relevantclinically translatabledevelopmentaleffective therapyeffective treatmentelectroporative deliveryfightinggene electrotransferhost responseimage guidanceimage guidedimmune competentimmune system responseimmunoresponseimmunosuppressed patientimprovedin vivoinjuriesinstrumentionizationmalignancymechanicmechanicalmillimetermodel of animalmouse modelmurine modelneoplasm progressionneoplasm/cancerneoplastic progressionnew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapy approachesnew treatment approachnew treatment strategynovelnovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapy approachpancreatic cancer cellspancreatic cancer modelpancreatic cancer patientspancreatic malignancypancreatic neoplasiapancreatic neoplasmpancreatic tumor cellspancreatic tumor modelpatient derived xenograft modelpatients with pancreatic cancerphysical propertypig modelpiglet modelporcineporcine modelpost treatmentpre-clinicalpreclinicalpreservationpreventpreventingradiation or chemotherapyreal-time imagesrealtime imageresponsesuidswine modeltranslation to humanstreatment strategytumortumor ablationtumor progressiontumor xenograftvascular
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Full Description

PROJECT SUMMARY: Pancreatic cancer accounts for approximately 3% of all cancers in the United States
and approximately 7% of all cancer related deaths. New treatment paradigms are direly needed. Emerging tumor

ablation techniques have shown significant promise in both clinical and pre-clinical cancer studies. This proposal

will focus on histotripsy, which is the first non-invasive, non-ionizing, non-thermal, image-guided tumor ablation

modality that destroys tumors through the precise control of acoustic cavitation and is capable of overcoming

many of the limitations of the other tumor ablation modalities currently under development for this malignancy.

Recently, our research team completed proof-of-concept studies demonstrating that histotripsy is effective at

targeting the pancreas and produces consistent, fast, and complete ablations, even in proximity to critical

structures. Intriguingly, work by our team and others has also shown that histotripsy is effective in inducing

systemic anti-tumor responses, resulting in post-treatment tumor regression both locally and at metastatic sites.

However, the exact mechanism and level of control of this phenomenon is still unclear. The objective of this

proposal is to utilize our pre-clinical mouse and novel pig animal models to expand upon the preliminary data

presented in this proposal to generate critical mechanistic, safety, and efficacy data necessary to support future

clinical trials in pancreatic cancer patients. Our overarching hypothesis is that histotripsy can achieve safe and

selective focal ablation of pancreatic tumors and improve systemic anti-tumor immune responses. SPECIFIC

AIM 1: Determine histotripsy treatment parameters for precise and complete pancreatic tumor ablation.

Our preliminary data demonstrates the general feasibility of histotripsy ablation in the pancreas. This Aim will

test the hypothesis that histotripsy can achieve precise, efficient, and complete ablation of pancreatic tumors

without injuring critical structures, such as major blood vessels, bile ducts, and intestines. SPECIFIC AIM 2:

Establish histotripsy treatment strategies for pancreatic cancer that optimize tumor ablation and

systemic anti-tumor immune responses. This Aim will test the hypothesis that histotripsy is an effective

treatment modality for precise and complete pancreatic tumor ablation in vivo. We also postulate that due to the

unique features of histotripsy, focal tumor ablation results in predictable and tunable systemic anti-tumor host

immune responses reducing metastatic burden and preventing recurrence. SPECIFIC AIM 3: Define histotripsy

treatment parameters and determine its safety profile utilizing physiologically and clinically relevant

porcine models of pancreatic cancer. Pigs better mimic human patients in terms of anatomy, size, and

instrument scale. This Aim will test the hypothesis that histotripsy parameters can be established to effectively

ablate orthotopic pancreatic tumors under physiologically and clinically relevant in situ conditions.

SIGNIFICANCE: The studies outlined in this proposal will demonstrate the safety and efficacy of histotripsy for

pancreatic cancer ablation and will provide critical data necessary for clinical translation to human patients.

Grant Number: 5R01CA269811-05
NIH Institute/Center: NIH

Principal Investigator: Irving Allen

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