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Submitted
Abstract
Abstract Title
Oncological and functional outcome of repeat irreversible electroporation for recurrent prostate cancer after primary electroporation
Presentation Type
Podium Abstract
Manuscript Type
Clinical Research
Abstract Category *
Oncology: Prostate
Author's Information
Number of Authors (including submitting/presenting author) *
5
No more than 10 authors can be listed (as per the Good Publication Practice (GPP) Guidelines).
Please ensure the authors are listed in the right order.
Country
Australia
Co-author 1
Daniel Feng d.feng1996@gmail.com St. Vincent's Prostate Cancer Research Centre Sydney Australia *
Co-author 2
Matthijs Scheltema d.feng1996@gmail.com St. Vincent's Prostate Cancer Research Centre Sydney Australia -
Co-author 3
Bart Geboers d.feng1996@gmail.com St. Vincent's Prostate Cancer Research Centre Sydney Australia -
Co-author 4
Shikha Agrawal d.feng1996@gmail.com St. Vincent's Prostate Cancer Research Centre Sydney Australia -
Co-author 5
Phillip Stricker d.feng1996@gmail.com St. Vincent's Prostate Cancer Research Centre Sydney Australia -
Co-author 6
Co-author 7
Co-author 8
Co-author 9
Co-author 10
Co-author 11
Co-author 12
Co-author 13
Co-author 14
Co-author 15
Co-author 16
Co-author 17
Co-author 18
Co-author 19
Co-author 20
Abstract Content
Introduction
As focal therapy becomes more common for localised prostate cancer, the question arises: how do we treat recurrences following focal therapy failure? One option is to deliver a second treatment if the recurrence is localised. This study aims to evaluate the success of a second irreversible electroporation treatment after failure of primary irreversible electroporation.
Materials and Methods
All patients that underwent redo IRE in the period between February 2013 and February 2024 with a minimum 12 months of follow-up were analysed. Follow-up included 6-month magnetic resonance imaging (MRI) and standardised transperineal saturation template ± targeted biopsies at 12 months, and further biopsies in the case of clinical suspicion on serial imaging and/or prostate-specific antigen (PSA) levels. Failure-free survival (FFS) was defined as no progression to radical treatment.
Results
A total of 36 patients were analysed. 44.4% (16/36) had a clinically significant recurrence (ISUP 2 or greater). Of those patients 8.3% (3/36) were suitable for active surveillance, 5.6% had a third IRE treatment (2/36), 16.7% (6/36) underwent salvage radical prostatectomy, and 13.9% (5/36) underwent salvage radiotherapy. Overall, 63.9% achieved good local control after 2 IRE treatments (defined as not needing salvage radical treatment or >2 IRE treatments). Data on functional outcomes including continence and erectile function are currently being analysed.
Conclusions
For patients who have prostate cancer recurrence after primary IRE treatment, a second IRE treatment achieve good control in the majority of cases and is safe. This is particularly significant for those patients who are not surgical candidates, who have had previous pelvic radiotherapy for other malignancies, or who are strongly focused on maintaining their erectile function and continence.
Keywords
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Character Count
1817
Vimeo Link
Presentation Details
Session
Free Paper Podium(25): Oncology Prostate (F)
Date
Aug. 17 (Sun.)
Time
14:06 -14:12
Presentation Order
7