AI Article Synopsis

  • Prostate cancer recurrences post-initial non-surgical treatment are mainly treated with androgen-deprivation therapy (ADT), but salvage radical prostatectomy (sRP) poses higher risks, prompting exploration of alternative treatments like salvage irreversible electroporation (sIRE).
  • A pilot study (SAFE) evaluated the safety and effectiveness of sIRE in 20 patients with localized recurrent prostate cancer after prior treatments, using advanced imaging and patient evaluations.
  • Initial findings suggest sIRE could be a viable and safer curative option for recurrent prostate cancer, with fewer side effects compared to traditional sRP approaches.

Article Abstract

Introduction: Currently, the majority of prostate cancer (PCa) recurrences after non-surgical first-line treatment are managed with androgen-deprivation therapy (ADT). Salvage radical prostatectomy (sRP) is a curative alternative to ADT but yields significant morbidity. Preliminary evidence from focal salvage treatments shows similar oncological control but lower morbidity compared to sRP. Among available ablative focal energies, irreversible electroporation (IRE) is a treatment modality that proved promising, especially in treating apical lesions, where PCa most often recurs. Our aim is to test the safety of salvage IRE for recurrent PCa.

Methods: We performed a single-arm pilot feasibility study (IDEAL stage 2a): SAFE, SAlvage Focal irreversible Electroporation for recurrent localized PCa. Twenty patients with biopsy-proven PCa recurrence after primary non-surgical (radiation or ablation) treatment were included. All men will undergo mpMRI ± targeted biopsies, pre-operative PSMA-PET staging before inclusion and sIRE. Outcomes will be evaluated through internationally validated questionnaires and morbidity scales. All men will undergo a control biopsy at one year.

Results: Primary objectives were the evaluation of the safety of sIRE (and patients' quality of life) after treatment. Secondary objectives were the evaluation of functional outcomes, namely, continence and erectile function changes and evaluation of short-term oncological efficacy.

Conclusions: SAFE is the second pilot study to evaluate sIRE and the first one performed according to the most recent diagnostic and staging imaging standards. sIRE may provide a curative option for recurrent PCa together with lower comorbidities compared to sRP.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9209638PMC
http://dx.doi.org/10.3389/fsurg.2022.900528DOI Listing

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