The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Irreversible Electroporation: Implications for Prostate Ablation
Open accessAbstract
Percutaneous prostate cryo-ablation has become an accepted treatment for primary prostate cancer. Thermal tissue ablation based on cold, however, does have some distinct limitations. These include, variable damage at the cryo lesions margin, injury to adjacent structures such as rectum, urethra and NVB (neurovascular bundle), and long procedure time due to the need for multiple freeze thaw cycles, that have limited the acceptance of this modality. Irreversible electroporation IRE, is a new non-thermal ablation modality that uses short pulses of DC electric current to create irreversible pore in the cell membrane, thus, causing cell death. This method theoretically should have significant advantages in ablating prostate tissue. Six males dogs had their prostates treated using IRE. Pulses were applied using a DC generator that delivered pulses in the microsecond range of duration, with a variable pulse interval and voltage range. IRE probes were placed percutaneously or trans-rectally using trans-rectal ultrasound guidance. In one of the dogs, the lesions were made purposely to include the rectum, urethra, and neurovascular bundle (NVB). Subjects were followed for 1 to 14 days before sacrifice. IRE lesions in the prostate had unique characteristics compared to thermal lesions. The margins of the IRE lesions was very distinct with a narrow zone of transition from normal to complete necrosis, there was complete destruction within the IRE lesion, and rapid resolution of the lesions with marked shrinkage within two weeks. Structures such as urethra, vessels, nerves, and rectum were unaffected by the IRE application. IRE lesions have characteristics that are distinctly different than thermal lesions. The differences could be very advantageous in a clinical setting, improving the results and acceptance of prostate ablation.
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Citations
Cites
Gene transfer into mouse lyoma cells by electroporation in high electric fields.
Neumann, E., Schaefer-Ridder, M., Wang, Y., & Hofschneider, P. H. (1982) · The EMBO Journal · doi:10.1002/j.1460-2075.1982.tb01257.x · Cited by 2,502
Tissue Ablation with Irreversible Electroporation
Davalos, R. V., Mir, L. M., & Rubinsky, B. (2005) · Annals of Biomedical Engineering · doi:10.1007/s10439-005-8981-8 · Cited by 1,293
Self-citationIrreversible Electroporation: A New Ablation Modality — Clinical Implications
Rubinsky, B., Onik, G., & Mikus, P. (2007) · Technology in Cancer Research & Treatment · doi:10.1177/153303460700600106 · Cited by 781
Self-citationFrom the Health Care Financing Administration
Wilensky, G. R. (1991) · JAMA: The Journal of the American Medical Association · doi:10.1001/jama.1991.03470200020007 · Cited by 635
Cancer Cells Ablation with Irreversible Electroporation
Miller, L., Leor, J., & Rubinsky, B. (2005) · Technology in Cancer Research & Treatment · doi:10.1177/153303460500400615 · Cited by 298
Self-citation[Electrochemotherapy, a new antitumor treatment: first clinical trial].
Mir, L. M., Belehradek, M., Domenge, C., Orlowski, S., Poddevin, B., Belehradek, J., Schwaab, G., Luboinski, B., & Paoletti, C. (1991) · PubMed · Cited by 272
Cited by
Principles of and Advances in Percutaneous Ablation
Ahmed, M., Brace, C. L., Lee, F. T., & Goldberg, S. N. (2011) · Radiology · doi:10.1148/radiol.10081634 · Cited by 916
A Review of Basic to Clinical Studies of Irreversible Electroporation Therapy
Jiang, C., Davalos, R. V., & Bischof, J. C. (2015) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2014.2367543 · Cited by 332
Mechanisms of cryoablation: Clinical consequences on malignant tumors
Baust, J. G., Gage, A. A., Bjerklund Johansen, T. E., & Baust, J. M. (2014) · Cryobiology · doi:10.1016/j.cryobiol.2013.11.001 · Cited by 239
Irreversible electroporation (NanoKnife) in cancer treatment
Jourabchi, N., Beroukhim, K., Tafti, B. A., Kee, S. T., & Lee, E. W. (2014) · Gastrointestinal Intervention · doi:10.1016/j.gii.2014.02.002 · Cited by 99
Metadata
- Authors
- Onik, G., Mikus, P., & Rubinsky, B.
- Venue
- Technology in Cancer Research & Treatment
- Publisher
- SAGE Publications
- Published
- 2007-08
- Volume
- 6
- Issue
- 4
- Pages
- 295-300
- ISSN
- 1533-0338 (ISSN-L)
- 1533-0346
- OpenAlex
- W2112143708
- Cited by
- 375
- References
- 6
- FWCI
- 13.04
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.