Histotripsy Methods for Pancreatic Cancer
| dc.contributor.author | Gannon, Jessica Mae | en |
| dc.contributor.committeechair | Vlaisavljevich, Eli | en |
| dc.contributor.committeemember | Brown, Jeremy | en |
| dc.contributor.committeemember | Allen, Irving Coy | en |
| dc.contributor.committeemember | Maxwell, Adam Douglas | en |
| dc.contributor.committeemember | Han, Aiguo | en |
| dc.contributor.department | Department of Biomedical Engineering and Mechanics | en |
| dc.date.accessioned | 2026-06-05T08:01:45Z | en |
| dc.date.available | 2026-06-05T08:01:45Z | en |
| dc.date.issued | 2026-06-04 | en |
| dc.description.abstract | Histotripsy is a focused ultrasound ablation modality that uses nanometer-sized endogenous gas nuclei to form a cloud of microbubbles to mechanically disintegrate tissue. The key features of histotripsy are that it is non-invasive, non-thermal, and non-ionizing. By applying microsecond-length, high pressure (> 15 MPa) pulses, these nuclei can rapidly expand and collapse, inducing high stress and strain on the surrounding tissue leading to cell rupture. The cavitation "bubble cloud" has millimeter precision to achieve clear boundaries between treated and untreated tissue. Histotripsy treatments can be monitored in real-time with B-mode ultrasound (US) imaging, where the bubble cloud appears as a bright hyperechoic region due to the strong scattering of acoustic energy by the bubbles. Previous work has shown that histotripsy can be tissue-selective with stiffer tissues being more resistant to the therapy due to their mechanical properties leading to preservation of critical structures like vessels and ducts. The feasibility and safety of histotripsy has been well-established for the treatment of liver cancer, both pre-clinically and clinically, but has yet to be developed for pancreatic cancer. The majority of pancreatic cancer patients are diagnosed late-stage, presenting with locally advanced or metastatic disease, leading to a select few that are candidates for surgery. Chemotherapy, radiation therapy, or a combination of the two have been used as front-line treatment options for patients albeit limited. While current ablative strategies have improved mortality rates, the overall survival for patients is still dismal. The main limitations of these ablative strategies are a lack of targeting precision and real-time treatment feedback as well as risk of damage to critical structures and inducing pancreatitis, along with other adverse events, given the sensitive nature of the pancreas. This dissertation investigates the safety and feasibility of using ultrasound-guided histotripsy to ablate pancreatic tissue with non-invasive and endo-surgical approaches. The research described herein 1) explores the feasibility of applying histotripsy trans-abdominally to healthy porcine pancreas, 2) evaluates histotripsy's safety profile in the pancreas of a large porcine model in vivo, and 3) establishes the feasibility of endoscopic histotripsy transducers for surgical and trans-gastric pancreas ablation. Future work will build on these studies to optimize histotripsy treatments for pancreatic tumors and further develop alternative endo-surgical histotripsy devices for improved targeting of these and other tumor types in anatomically challenging locations. | en |
| dc.description.abstractgeneral | Pancreatic cancer is a deadly disease with an extremely low 5-year relative survival rate of only 13%. The majority of patients present with tumors located near critical vasculature and metastasis to organs beyond the pancreas, making them ineligible for surgery. Chemotherapy, radiation therapy, or a combination of the two have been used as front-line treatment options for patients but with limited efficacy. Other strategies have investigated ablative therapies which apply extreme forms of energy such as heat, cold, or electrical pulses to tumors. While current ablative strategies have improved mortality rates, the overall survival for patients is still dismal. The main limitations of these ablative strategies are a lack of targeting precision and real-time treatment feedback as well as risk of damage to critical structures and inducing pancreatitis, along with other adverse events, given the sensitive nature of the pancreas. There is an urgent need for alternative treatment strategies for patients. Histotripsy is a focused ultrasound ablation modality that is non-invasive, non-thermal, and non-ionizing. High- pressure (> 15 MPa) sound waves are focused to a singular point to generate cavitation, which is referred to as the histotripsy "bubble cloud." The cloud contains microbubbles that rapidly expand and violently collapse to produce sufficient stresses and strains capable of mechanically destroying the targeted tissue. Histotripsy can achieve millimeter precision with clear boundaries between treated and untreated tissue. Treatments can be monitored in real-time with B-mode ultrasound (US) imaging, where the bubble cloud appears as a bright white region due to the strong scattering of acoustic energy by the bubbles. Previous work has shown that histotripsy can be tissue-selective with stiffer tissues being more resistant to the therapy due to their mechanical properties leading to preservation of critical structures like vessels and ducts. The feasibility and safety of histotripsy have been well-established for the treatment of liver cancer, both pre-clinically and clinically, but have yet to be developed for pancreatic cancer. This dissertation investigates the safety and feasibility of using ultrasound-guided histotripsy to ablate pancreatic tissue with non-invasive and endoscopic/surgical approaches. The research described herein 1) explores the feasibility of applying histotripsy trans-abdominally to healthy porcine pancreas, 2) evaluates histotripsy's safety profile in the pancreas of a large porcine model in vivo, and 3) establishes the feasibility of high-frequency histotripsy transducers for precise handheld surgical treatments and endoscopic therapy delivery through the stomach wall for trans-gastric pancreas ablation. Future work will build on these studies to optimize histotripsy treatments for pancreatic tumors and further develop alternative endo-surgical histotripsy devices for improved targeting of these and other tumor types in anatomically challenging locations. | en |
| dc.description.degree | Doctor of Philosophy | en |
| dc.format.medium | ETD | en |
| dc.identifier.other | vt_gsexam:46913 | en |
| dc.identifier.uri | https://hdl.handle.net/10919/143263 | en |
| dc.language.iso | en | en |
| dc.publisher | Virginia Tech | en |
| dc.rights | In Copyright | en |
| dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
| dc.subject | histotripsy | en |
| dc.subject | focused ultrasound | en |
| dc.subject | pancreas | en |
| dc.subject | non-invasive | en |
| dc.subject | endoscopic | en |
| dc.title | Histotripsy Methods for Pancreatic Cancer | en |
| dc.type | Dissertation | en |
| thesis.degree.discipline | Biomedical Engineering | en |
| thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
| thesis.degree.level | doctoral | en |
| thesis.degree.name | Doctor of Philosophy | en |
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