Investigation of High Frequency Irreversible Electroporation for Canine Spontaneous Primary Lung Tumor Ablation

dc.contributor.authorHay, Alayna N.en
dc.contributor.authorAycock, Kenneth N.en
dc.contributor.authorLorenzo, Melvin F.en
dc.contributor.authorDavid, Kaileeen
dc.contributor.authorCoutermarsh-Ott, Sherylen
dc.contributor.authorSalameh, Zaiden
dc.contributor.authorCampelo, Sabrina N.en
dc.contributor.authorArroyo, Julio P.en
dc.contributor.authorCiepluch, Brittanyen
dc.contributor.authorDaniel, Gregoryen
dc.contributor.authorDavalos, Rafael V.en
dc.contributor.authorTuohy, Joanneen
dc.date.accessioned2024-10-01T12:53:48Zen
dc.date.available2024-10-01T12:53:48Zen
dc.date.issued2024-09-07en
dc.date.updated2024-09-27T13:18:23Zen
dc.description.abstractIn this study, the feasibility of treating canine primary lung tumors with high-frequency irreversible electroporation (H-FIRE) was investigated as a novel lung cancer treatment option. H-FIRE is a minimally invasive tissue ablation modality that delivers bipolar pulsed electric fields to targeted cells, generating nanopores in cell membranes and rendering targeted cells nonviable. In the current study, canine patients (<i>n</i> = 5) with primary lung tumors underwent H-FIRE treatment with an applied voltage of 2250 V using a 2-5-2 &micro;s H-FIRE waveform to achieve partial tumor ablation prior to the surgical resection of the primary tumor. Surgically resected tumor samples were evaluated histologically for tumor ablation, and with immunohistochemical (IHC) staining to identify cell death (activated caspase-3) and macrophages (IBA-1, CD206, and iNOS). Changes in immunity and inflammatory gene signatures were also evaluated in tumor samples. H-FIRE ablation was evident by the microscopic observation of discrete foci of acute hemorrhage and necrosis, and in a subset of tumors (<i>n</i> = 2), we observed a greater intensity of cleaved caspase-3 staining in tumor cells within treated tumor regions compared to adjacent untreated tumor tissue. At the study evaluation timepoint of 2 h post H-FIRE, we observed differential gene expression changes in the genes <i>IDO1</i>, <i>IL6</i>, <i>TNF</i>, <i>CD209</i>, and <i>FOXP3</i> in treated tumor regions relative to paired untreated tumor regions. Additionally, we preliminarily evaluated the technical feasibility of delivering H-FIRE percutaneously under CT guidance to canine lung tumor patients (<i>n</i> = 2). Overall, H-FIRE treatment was well tolerated with no adverse clinical events, and our results suggest H-FIRE potentially altered the tumor immune microenvironment.en
dc.description.versionPublished versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationHay, A.N.; Aycock, K.N.; Lorenzo, M.F.; David, K.; Coutermarsh-Ott, S.; Salameh, Z.; Campelo, S.N.; Arroyo, J.P.; Ciepluch, B.; Daniel, G.; Davalos, R.V.; Tuohy, J. Investigation of High Frequency Irreversible Electroporation for Canine Spontaneous Primary Lung Tumor Ablation. Biomedicines 2024, 12, 2038.en
dc.identifier.doihttps://doi.org/10.3390/biomedicines12092038en
dc.identifier.urihttps://hdl.handle.net/10919/121236en
dc.language.isoenen
dc.publisherMDPIen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjecttumor ablationen
dc.subjectlung canceren
dc.subjectcomparative oncologyen
dc.subjectcanine oncologyen
dc.titleInvestigation of High Frequency Irreversible Electroporation for Canine Spontaneous Primary Lung Tumor Ablationen
dc.title.serialBiomedicinesen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten

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