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The SAFE Pilot Trial-SAlvage Focal Irreversible Electroporation-For Recurrent Localized Prostate Cancer: Rationale and Study Protocol.
Marra, Giancarlo; Shah, Taimur T; D'Agate, Daniele; Marquis, Alessandro; Calleris, Giorgio; Lunelli, Luca; Filippini, Claudia; Oderda, Marco; Gatti, Marco; Valerio, Massimo; Sanchez-Salas, Rafael; Bossi, Alberto; Gomez-Rivas, Juan; Conte, Francesca; Deandreis, Desiree; Cussenot, Olivier; Ricardi, Umberto; Gontero, Paolo.
  • Marra G; Department of Surgical Sciences and Urology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Shah TT; Department of Urology and Clinical Research Group on Predictive Onco-Urology, APHP, Sorbonne University Paris, Paris, France.
  • D'Agate D; Department of Urology, Imperial College, London, United Kingdom.
  • Marquis A; Department of Surgical Sciences and Urology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Calleris G; Department of Surgical Sciences and Urology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Lunelli L; Department of Surgical Sciences and Urology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Filippini C; Department of Urology and Clinical Research Group on Predictive Onco-Urology, APHP, Sorbonne University Paris, Paris, France.
  • Oderda M; Department of Surgical Sciences and Urology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Gatti M; Department of Surgical Sciences and Urology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Valerio M; Department of Surgical Sciences and Radiology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Sanchez-Salas R; Department of Urology, Centre Hospitalier-Universitaire Vaudois, CHUV, Lausanne, Switzerland.
  • Bossi A; Department of Urology, McGill University, Montreal, Canada.
  • Gomez-Rivas J; Department of Radiotherapy, Institut Gustave Roussy, Villejuif, France.
  • Conte F; Department of Urology, Hospital Clínico San Carlos, Madrid, Spain.
  • Deandreis D; Department of Surgical Sciences and Urology Clinic, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Cussenot O; Department of Nuclear Medicine, University of Turin and Città della Salute e della Scienza, Turin, Italy.
  • Ricardi U; Department of Urology and Clinical Research Group on Predictive Onco-Urology, APHP, Sorbonne University Paris, Paris, France.
  • Gontero P; Division of Radiotherapy and Department of Oncology, University of Turin and Città della Salute e della Scienza, Turin, Italy.
Front Surg ; 9: 900528, 2022.
Article en En | MEDLINE | ID: mdl-35747441
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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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Año: 2022 Tipo del documento: Article