Madeline I Foo, Cynthia Uzoukwu, Robert Morhard, Katrina L Falk, Bradford J Wood, Gregory Frey, Timothy J Ziemlewicz, Eli Vlaisavljevich, Beau B Toskich, Alissa Hendricks-Wenger
{"title":"Understanding histotripsy ablation safety: a systematic review of pre-clinical and clinical adverse events.","authors":"Madeline I Foo, Cynthia Uzoukwu, Robert Morhard, Katrina L Falk, Bradford J Wood, Gregory Frey, Timothy J Ziemlewicz, Eli Vlaisavljevich, Beau B Toskich, Alissa Hendricks-Wenger","doi":"10.1007/s44343-026-00062-2","DOIUrl":null,"url":null,"abstract":"<p><p>Histotripsy is the first cavitation-based ablation modality. Given limited clinical experience, synthesis of pre-clinical and early clinical data is essential to guide safe adoption. A PubMed and SCOPUS search was performed focused on pre-clinical and clinical adverse events (AEs) from Histotripsy ablation of parenchymal tissues in vivo (<i>n</i> = 141 total studies, <i>n</i> = 27 clinical reports). Early data suggest an acceptable acute safety profile in select settings; however, reports of serious AEs including pre-clinical bowel perforations, clinical acute kidney injuries, clinical vascular injuries and thromboses, and a clinical case report of hyperprogression raise caution. These highlight the need for proper technique, understanding of mechanism nuances, and longer-term follow-up to assess effects. Recognition of mechanism-specific AEs provides a framework to guide future assessments and safer adoption of Histotripsy. <b>Level of Evidence</b> No level of evidence (review).</p>","PeriodicalId":521157,"journal":{"name":"CVIR oncology","volume":"2 1","pages":"33"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13658349/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CVIR oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s44343-026-00062-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/12 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Histotripsy is the first cavitation-based ablation modality. Given limited clinical experience, synthesis of pre-clinical and early clinical data is essential to guide safe adoption. A PubMed and SCOPUS search was performed focused on pre-clinical and clinical adverse events (AEs) from Histotripsy ablation of parenchymal tissues in vivo (n = 141 total studies, n = 27 clinical reports). Early data suggest an acceptable acute safety profile in select settings; however, reports of serious AEs including pre-clinical bowel perforations, clinical acute kidney injuries, clinical vascular injuries and thromboses, and a clinical case report of hyperprogression raise caution. These highlight the need for proper technique, understanding of mechanism nuances, and longer-term follow-up to assess effects. Recognition of mechanism-specific AEs provides a framework to guide future assessments and safer adoption of Histotripsy. Level of Evidence No level of evidence (review).