Irreversible Electroporation and Beta-Glucan-Induced Trained Innate Immunity for Treatment of Pancreatic Ductal Adenocarcinoma: A Phase II Study.

Xiaoling Hu, Kelly M McMasters, Robert Cg Martin, Min Tan, Jun Yan, Hong Li, Yan Li, Emily A Shore, Danial A Malik, Traci Hayat

Journal: Journal of the American College of Surgeons 2025;240(4):351-361

PMID: 39840846

Abstract

BACKGROUND

Irreversible electroporation (IRE) has augmented the effects of certain immunotherapies in pancreatic ductal adenocarcinoma (PDA). Yeast-derived particulate beta-glucan induces trained innate immunity and successfully reduced murine pancreatic cancer burden. This is a phase II study to test the hypothesis that IRE may augment beta-glucan-induced trained immunity in patients with PDA.

STUDY DESIGN

In this phase II clinical trial (NCT03080974), surgical ablative IRE was performed on clinical stage III PDA followed by oral beta-glucan administration for 12 months or until disease recurrence. Peripheral blood was taken preoperative, 14 days, and every 3 months and was evaluated by mass cytometry and compared with patients who received IRE alone.

RESULTS

Thirty consecutive patients with preoperative clinical stage III PDA were treated with IRE and then initiated on oral beta-glucan postoperatively were compared with 20 patients treated with IRE alone. There were no dose-limiting toxicities with oral beta-glucan, and compliance with therapy was 96% in all patients. Seven patients (23%) developed grade 3 or 4 treatment-related adverse events at 90 days; none required a dose modification of oral beta-glucan. A median disease-free interval (DFI) was 18 months (range 6 to 48 months), with a median overall survival (OS) of 32.5 months (range 4 to 53 months). At 12 months post-IRE, immunophenotyping was demonstrated a significant effect with improvement in the IRE-beta-glucan-treated group. This also resulted in a significant decrease on naive CD4 and CD8 T cells with increased CD4 and CD8 terminal effector cells in the IRE-beta-glucan-treated group, which correlated with a significant improvement in DFI and OS (p = 0.001).

CONCLUSIONS

Combined beta-glucan with IRE-ablated PDA tumor cells elicited a potent trained response and augmented antitumor functionality at 12 months post-IRE, which translated into an improved DFI and OS.

Copyright © 2025 by the American College of Surgeons. Published by Wolters Kluwer Health, Inc. All rights reserved.

Address: From the Divisions of Surgical Oncology (Martin, Y Li, Shore, Malik, Hayat, Tan, McMasters), The Hiram C Polk Jr, MD, Department of Surgery, University of Louisville School of Medicine, Louisville, KY.; Functional Immunomics Core (H Li), Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY.; Immunotherapy (Hu, Yan), The Hiram C Polk Jr, MD, Department of Surgery, University of Louisville School of Medicine, Louisville, KY.; Immuno-Oncology Program (Hu, Yan), Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY.; Immunotherapy (Hu, Yan), The Hiram C Polk Jr, MD, Department of Surgery, University of Louisville School of Medicine, Louisville, KY.; Immuno-Oncology Program (Hu, Yan), Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY.; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY (Yan).
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