Irreversible electroporation, as a nonthermal therapy of prostate cancer, has been used
in clinic for several years. The mechanism of irreversible electroporation ablation is
thermal independent; thus, the main structures (eg, rectum, urethra, and neurovascular
bundle) in prostate are spared during the treatment, which leads to the retention of
prostate function. However, various clinical trials have shown that muscle contractions
occur during this therapy, which warrants deep muscle anesthesia. Use of high-frequency
bipolar pulses has been proposed to reduce muscle contractions during treatment, which has
already triggered a multitude of studies at the cellular and animal scale. In this study,
we first investigated the efficacy and safety of high-frequency bipolar pulses in human
prostate cancer ablation. There are 40 male patients with prostate cancer aged between 51
and 85 years involved in this study. All patients received 250 high-frequency bipolar
pulse bursts with the repeat frequency of 1 Hz. Each burst comprised 20 individual pulses
of 5 microseconds, so one burst total energized time was 100 microseconds. The number of
the electrodes ranged 2 to 6, depending on tumor size. A small amount of muscle relaxant
was still needed, so there were no visible muscle contractions during the pulse delivery
process. Four weeks after treatment, it was found that the ablation margins were distinct
in magnetic resonance imaging scans, and the prostate capsule and urethra were retained.
Eight patients underwent radical prostatectomy for pathological analysis after treatment,
and the results of hematoxylin and eosin staining revealed that the urethra and major
vasculature in prostate have been preserved. By overlaying the electric field contour on
the ablation zone, the electric field lethality threshold is determined to be 522 ± 74
V/cm. This study is the first to validate the feasibility of tumor ablation by
high-frequency bipolar pulses and provide valuable experience of irreversible
electroporation in clinical applications.
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