Irreversible electroporation ablation against subcutaneously implanted VX2 tumors in rabbits: findings of shearwave

Rui Chen1, Sheng Li2, Limei Wu3

  • 1Attending Doctor, Department of Ultrasound, the Second Affiliated Hospital of Guangzhou Medical University, China.

Scottish Medical Journal
|February 5, 2021
PubMed
Abstract

Insights

Irreversible electroporation (IRE) in VX2 tumors causes a temporary increase in stiffness, measured by shearwave ultrasound elastography (SWE), before returning to normal levels. This non-invasive method tracks stiffness changes during IRE ablation.

Area of Science:

  • Oncology
  • Medical Imaging
  • Biophysics

Background:

  • VX2 tumors are a common model for studying tumor ablation.
  • Irreversible electroporation (IRE) is an effective tumor ablation technique.
  • Shearwave ultrasound elastography (SWE) non-invasively measures tissue stiffness.

Purpose of the Study:

  • To evaluate changes in VX2 tumor stiffness before and after irreversible electroporation (IRE) ablation.
  • To assess the utility of shearwave ultrasound elastography (SWE) in monitoring IRE treatment.
  • To characterize the temporal changes in tumor stiffness following IRE.

Main Methods:

  • VX2 tumors were implanted subcutaneously in rabbits.
  • IRE was performed on 20 VX2 tumors.
  • Tumor stiffness was measured using SWE at baseline, 120 minutes, 7 days, and 14 days post-IRE.

Main Results:

  • Mean tumor stiffness (Emean) increased significantly from 10.45 ± 1.07 KPa before IRE to 70.53 ± 9.87 KPa at 120 minutes post-IRE.
  • Tumor stiffness decreased to 40.22 ± 9.01 KPa at 7 days and 15.17 ± 1.00 KPa at 14 days post-IRE.
  • Pathological examination revealed a clear boundary between the ablated area and normal tissue.

Conclusions:

  • Tumor stiffness following IRE exhibits an initial rise and subsequent normalization.
  • SWE is a valuable non-invasive tool for assessing tissue stiffness during different stages of IRE ablation.
  • These findings contribute to understanding the biophysical changes induced by IRE in tumors.

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