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Review Article |

Irreversible Electroporation for the Ablation of Liver Tumors:  Are We There Yet?

Kevin P. Charpentier, MD
Arch Surg. 2012;147(11):1053-1061. doi:10.1001/2013.jamasurg.100.
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Published online

Objective  To explore irreversible electroporation (IRE) as a novel, nonthermal form of tissue ablation using high-voltage electrical current to induce pores in the lipid bilayer of cells, resulting in cell death.

Data Sources  PubMed searches were performed using the keywords electroporation, IRE, and ablation. The abstracts for the 2012 meetings of both the American Hepato-Pancreato-Biliary Association and the Society for Interventional Radiology were also searched. All articles and abstracts with any reference to electroporation were identified and reviewed.

Study Selection  All studies and abstracts pertaining to electroporation.

Data Extraction  All data pertaining to the safety and efficacy of IRE were extracted from preclinical and clinical studies. Preclinical data detailing the theory and design of IRE systems were also extracted.

Data Synthesis  Preclinical studies have suggested that IRE may have advantages over conventional forms of thermal tumor ablation including no heat sink effect and preservation of the acellular elements of tissue, resulting in less unwanted collateral damage. The early clinical experience with IRE demonstrates safety for the ablation of human liver tumors. Short-term data regarding oncologic outcome is now emerging and appears encouraging.

Conclusion  Irreversible electroporation is likely to fill a niche void for the ablation of small liver tumors abutting a major vascular structure and for ablation of tumors abutting a major portal pedicle where heat sink and collateral damage must be avoided for maximum efficacy and safety. Studies are still needed to define the short-term and long-term oncologic efficacy of IRE.

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Figures

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Figure 1. Local failure of thermal ablation owing to heat sink. A 67-year-old woman presented with left-sided colon cancer and synchronous, bilobar liver metastases. Following resection of the colon primary, she was treated with 8 cycles of leucovorin, fluorouracil, and oxaliplatin, as well as bevacizumab (Avastin). She was deemed unresectable owing to concerns about functional liver reserve and was treated by microwave ablation of tumors in segments 7 and 4a. A, The tumor in segment 4a (thick arrow) measuring 2.7 cm and abutting the left hepatic vein (thin arrow). B, Positron-emission tomographic scan image depicting increased fluorodeoxyglucose activity (thick arrow) in segment 4a, consistent with residual tumor adjacent to the left hepatic vein (thin arrow). Heat sink was implicated as a possible contributing cause of the residual disease. She is alive 3 years after initial diagnosis.

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Figure 2. Collateral damage following thermal ablation. A 76-year-old woman underwent laparoscopic microwave ablation for multifocal hepatocellular carcinoma. A, A hepatoma (thick arrow) abutting the segment 7 portal pedicle (thin arrow). B, Infarction of segment 7 as a result of collateral damage to the segment 7 portal pedicle during microwave ablation. The patient went on to a full recovery and is alive 28 months following initial ablation.

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Figure 3. Hemorrhagic necrosis following irreversible electroporation of the liver. Hematoxylin and eosin stain of liver tissue 48 hours after irreversible electroporation showing hemorrhagic necrosis of the hepatocytes with preservation of the portal vein (thick arrow) and bile ducts (thin arrows). Original magnification ×20.

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Figure 4. Absence of heat sink following irreversible electroporation of the liver. Liver tissue is shown following ablation by irreversible electroporation. A, The arrow highlights a hepatic vein in the center of the ablation zone, with hepatocyte cell death immediately adjacent to the vein. B, Hematoxylin and eosin staining confirms hemorrhagic necrosis of the hepatocytes immediately adjacent to the central vein without evidence of heat sink. Original magnification ×4.

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Figure 5. Irreversible electroporation of the liver hilum. A, Liver tissue following ablation with irreversible electroporation showing preservation of the bile duct (BD), hepatic artery (HA), and portal vein (PV) within the zone of ablation. B, Liver tissue stained with triphenyltetrazolium chloride following IRE ablation of the hilum including the portal pedicle. The viable tissue retains the red triphenyltetrazolium chloride dye, while the area of ablation does not. The arrow highlights a patent, preserved portal vein in the center of the ablation zone.

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Figure 6. Triphenyltetrazolium chloride staining following irreversible electroporation of the liver. Liver tissue explanted 2 hours after ablation with irreversible electroporation and stained with triphenyltetrazolium chloride. Viable hepatocytes retain the red dye. The zone of ablation does not retain the triphenyltetrazolium chloride stain.

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