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IEEE Transactions on Biomedical Engineering

Authors :
Lauren Ruger
Ester Yang
Jessica Gannon
Hannah Sheppard
Sheryl Coutermarsh-Ott
Timothy J. Ziemlewicz
Nikolaos Dervisis
Irving C. Allen
Gregory B. Daniel
Joanne Tuohy
Eli Vlaisavljevich
Shawna Klahn
Source :
IEEE Trans Biomed Eng
Publication Year :
2022
Publisher :
Institute of Electrical and Electronics Engineers (IEEE), 2022.

Abstract

Introduction: Histotripsy is a non-invasive focused ultrasound therapy that uses controlled acoustic cavitation to mechanically disintegrate tissue. To date, there are no reports investigating histotripsy for the treatment of soft tissue sarcoma (STS). Objective: This study aimed to investigate the in vivo feasibility of ablating STS with histotripsy and to characterize the impact of partial histotripsy ablation on the acute immunologic response in canine patients with spontaneous STS. Methods: A custom 500 kHz histotripsy system was used to treat ten dogs with naturally occurring STS. Four to six days after histotripsy, tumors were surgically resected. Safety was determined by monitoring vital signs during treatment and post-treatment physical examinations, routine lab work, and owners’ reports. Ablation was characterized using radiologic and histopathologic analyses. Systemic immunological impact was evaluated by measuring changes in cytokine concentrations, and tumor microenvironment changes were evaluated by characterizing changes in infiltration with tumor-associated macrophages (TAMs) and tumor-infiltrating lymphocytes (TILs) using multiplex immunohistochemistry and differential gene expression. Results: Results showed histotripsy ablation was achievable and well-tolerated in all ten dogs. Immunological results showed histotripsy induced pro-inflammatory changes in the tumor microenvironment. Conclusion & Significance: Overall, this study demonstrates histotripsy's potential as a precise, non-invasive treatment for STS. Published version

Details

Database :
OpenAIRE
Journal :
IEEE Trans Biomed Eng
Accession number :
edsair.doi.dedup.....5663fadc0fa1072525c0e8a76e69efd9