Evidence map›Paper›PMID 42588651›Full record

ArticleCancers2026

Safe and Effective Histotripsy Ablation of Human Liver Tumors in a Genetically Modified Porcine Model.

Tamalika Paul, Jessica Gannon, Manali Powar, Cora Youngs, Cassandra S Poole, Carley M Elliott, Mackenzie K Woolls, Khan Imran Mohammad, Sherrie Clark-Deener, Christopher Byron and 7 more

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Tamalika PaulDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.ORCID 0000-0002-4888-5915
Jessica GannonDepartment of Biomedical Engineering and Mechanics, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Manali PowarGraduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Roanoke, VA 24016, USA.ORCID 0009-0001-4611-1342
Cora YoungsCollege of Science, Virginia Tech, Blacksburg, VA 24061, USA.
Cassandra S PooleDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.ORCID 0009-0002-5992-9028
Carley M ElliottGraduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Roanoke, VA 24016, USA.ORCID 0009-0004-9685-6571
Mackenzie K WoollsGraduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Roanoke, VA 24016, USA.ORCID 0000-0003-0957-728X
Khan Imran MohammadGraduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Roanoke, VA 24016, USA.ORCID 0000-0003-0755-8499
Sherrie Clark-DeenerDepartment of Large Animal Clinical Sciences, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.ORCID 0000-0002-6620-0625
Christopher ByronDepartment of Large Animal Clinical Sciences, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.ORCID 0000-0003-1249-1364
Michael EdwardsDepartment of Small Animal Clinical Sciences, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.ORCID 0000-0003-3606-675X
Sheryl Coutermarsh-OttDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.ORCID 0000-0001-7385-3969
Kristin EdenDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.ORCID 0000-0001-5309-5830
Kiho LeeDivision of Animal Science, College of Agriculture Food and Natural Resources, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0003-1548-0513
Timothy J ZiemlewiczDepartment of Radiology, University of Wisconsin School of Medicine, Madison, WI 53705, USA.
Eli VlaisavljevichDepartment of Biomedical Engineering and Mechanics, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Irving C AllenDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA 24061, USA.

Funding

Developing Methods for Precise, Safe and Target-location Specific Histotripsy of Liver TumorsR01CA262474 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI ZIEMLEWICZ, TIMOTHY J · 2021 to 2025
$2.4M
Optimization of High Frequency Irreversible Electroporation (H-FIRE) for tumor ablation and immune system activation in pancreatic cancer applicationsR01CA274439 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI Irving C Allen · 2023 to 2026
$2.1M
Deploying Histotripsy Based Tumor Ablation Strategies to Treat Pancreatic CancerR01CA269811 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI Irving C Allen · 2022 to 2026
$2.0M
NCI NIH HHS R01 CA262474NCI NIH HHS R01 CA269811NCI NIH HHS R01 CA274439NIH HHS 1R01CA262474-04NIH HHS 1R01CA269811-05
6 · The paper itself

Abstract

backgroundLiver cancers are a major cause of morbidity and mortality in patients where effective, non-invasive treatment options remain limited.

objectiveHistotripsy is a non-invasive, non-thermal, image-guided focused ultrasound method of ablation that mechanically disrupts cells and offers a range of potential advantages over other ablation modalities. The lack of physiologically and anatomically relevant animal models of human liver cancer has significantly hindered biomedical device development, including histotripsy.

methodsTo address these limitations, we developed a clinically relevant large animal orthotopic, dual-tumor model of human liver cancer and utilized these unique animals to evaluate the safety and efficacy of histotripsy. Here, we utilized immunocompromised pigs with genetic modifications in their IL-2RG and RAG2 genes and orthotopically engrafted human hepatocellular carcinoma (HepG2/C3A) and pancreatic adenocarcinoma (Panc-1) cells within the liver. The models were designed to recapitulate primary and metastatic liver tumor phenotypes.

resultsHistotripsy enabled real-time visualization of the treatment by the formation of bubble clouds and accurate targeting of the lesions. Histological analysis confirmed the engraftment of tumor cells and the ablation of targeted tissue. Serum biomarkers demonstrated no significant differences in bilirubin, ALT, ALKP, or CK post-treatment, suggesting that histotripsy treatment was well tolerated with minimal hepatic dysfunction or hepatocellular injury.

conclusionsThese findings establish a novel, clinically relevant porcine model of primary and metastatic liver tumors and demonstrate the safety and feasibility of using this model for evaluating histotripsy as a noninvasive modality for precise tumor ablation.

Indexed as

cancerfocused ultrasoundhepatocellular carcinomapancreatic adenocarcinomapig

Identifiers

PMID42588651
PMCPMC13464800

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.