EUS-guided radiofrequency ablation for pancreatic adenocarcinoma
- PMID: 38729313
- DOI: 10.1016/j.gie.2024.04.2926
EUS-guided radiofrequency ablation for pancreatic adenocarcinoma
Abstract
Background and aims: Emerging data suggest neoadjuvant chemotherapy (NAC) for resectable pancreatic ductal adenocarcinoma (PDAC) is associated with improved survival. However, less than 40% of patients demonstrate a meaningful radiographic response to NAC. EUS-guided radiofrequency ablation (EUS-RFA) has emerged as a new modality to treat PDAC. We hypothesize that NAC plus EUS-RFA can be used in the management of resectable PDAC.
Methods: This was a prospective review of PDAC patients meeting the criteria of resectable tumor anatomy who underwent NAC chemotherapy plus EUS-RFA followed by pancreatic resection. Radiographic imaging and perioperative and short-term outcomes were recorded. Surgical pathology specimens were analyzed for treatment response.
Results: Three eligible patients with resectable PDAC received 4 months of NAC plus EUS-RFA. One month after completing NAC and EUS-RFA, all 3 patients underwent standard pancreaticoduodenectomy without adverse events. After a 6-week recovery, all patients completed 2 months of postoperative adjuvant chemotherapy.
Conclusions: In our institutional experience, this treatment protocol appears to be safe as patients tolerated the combination of chemotherapy and ablation. Patients underwent pancreatic resection with uneventful recovery. This novel neoadjuvant approach may provide a more effective alternative to chemotherapy alone.
Copyright © 2024 American Society for Gastrointestinal Endoscopy. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Disclosure The following author received research support for this study from Atilla Ertan MD Endowment funding: N. Thosani. In addition, the following authors disclosed financial relationships: P. Cen: Speaker for Merck and Pfizer; consultant for Astella, Eisai, and Taiho Oncology; advisory board for Merck and Pfizer. J. H. Rowe: Research support from Aveo Pharmaceuticals. J. M. Bailey: Research support from the National Institutes of Health. N. Thosani: Research support from Emcision; royalties from UpToDate; consultant for Boston Scientific and Pentax America; speaker for Abbvie; creatorship rights from RoseAId Inc. All other authors disclosed no financial relationships. Research support for this study was provided by Carolyn Frost Keenan and Charlie Gaines Research Endowment Funds to the Center for Interventional Gastroenterology at UTHealth.
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