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Is It Safe to Switch from a Standard Anterior to Retzius-Sparing Approach in Robot-Assisted Radical Prostatectomy?
Lambert, Edward; Allaeys, Charlotte; Berquin, Camille; De Visschere, Pieter; Verbeke, Sofie; Vanneste, Ben; Fonteyne, Valerie; Van Praet, Charles; Lumen, Nicolaas.
Afiliação
  • Lambert E; ERN eUROGEN Accredited Centre, Department of Urology, Ghent University Hospital, 9000 Ghent, Belgium.
  • Allaeys C; Junior ERUS/YAU Working Group on Robot-Assisted Surgery of the European Association of Urology, 6803 AA Arnhem, The Netherlands.
  • Berquin C; ERN eUROGEN Accredited Centre, Department of Urology, Ghent University Hospital, 9000 Ghent, Belgium.
  • De Visschere P; ERN eUROGEN Accredited Centre, Department of Urology, Ghent University Hospital, 9000 Ghent, Belgium.
  • Verbeke S; Department of Radiology and Nuclear Medicine, Ghent University Hospital, 9000 Ghent, Belgium.
  • Vanneste B; Department of Pathology, Ghent University Hospital, 9000 Ghent, Belgium.
  • Fonteyne V; Department of Radiation Oncology, Ghent University Hospital, 9000 Ghent, Belgium.
  • Van Praet C; Department of Radiation Oncology (MAASTRO), GROW-School for Oncology and Developmental Biology, Maastricht UMC, 6229 HX Maastricht, The Netherlands.
  • Lumen N; Department of Radiation Oncology, Ghent University Hospital, 9000 Ghent, Belgium.
Curr Oncol ; 30(3): 3447-3460, 2023 03 17.
Article em En | MEDLINE | ID: mdl-36975474
ABSTRACT

BACKGROUND:

Retzius-sparing robot-assisted radical prostatectomy (RS-RARP) has been shown to lead to better outcomes regarding early continence compared to standard anterior RARP (SA-RARP). The goal of this study was to assess the feasibility and safety of implementing RS-RARP in a tertiary center with experience in SA-RARP.

METHODS:

From February 2020, all newly diagnosed non-metastatic prostate cancer patients for whom RARP was indicated were evaluated for RS-RARP. Data from the first 100 RS-RARP patients were prospectively collected and compared with data from the last 100 SA-RARP patients. Patients were evaluated for Clavien Dindo grade ≥3a complications, urinary continence after 2 and 6 weeks, 3, 6 and 12 months, erectile function, positive surgical margins (PSMs) and biochemical recurrence (BCR).

RESULTS:

There was no significant difference in postoperative complications at Clavien-Dindo grade ≥3a (SA-RARP 6, RS-RARP 4; p = 0.292). At all time points, significantly higher proportions of RS-RARP patients were continent (p < 0.001). No significant differences in postoperative potency were observed (52% vs. 59%, respectively, p = 0.608). PSMs were more frequent in the RS-RARP group (43% vs. 29%, p = 0.034), especially in locally advanced tumors (pT3 64.6% vs. 43.8%, p = 0.041-pT2 23.5% vs. 15.4%, p = 0.329). The one-year BCR-free survival was 82.6% vs. 81.6% in the SA-RARP and RS-RARP groups, respectively (p = 0.567). The median follow-up was 22 [18-27] vs. 24.5 [17-35] months in the RS-RARP and SA-RARP groups, respectively (p = 0.008).

CONCLUSIONS:

The transition from SA-RARP to RS-RARP can be safely performed by surgeons proficient in SA-RARP. Continence results after RS-RARP were significantly better at any time point. A higher proportion of PSMs was observed, although it did not result in a worse BCR-free survival.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Robótica / Procedimentos Cirúrgicos Robóticos Limite: Humans / Male Idioma: En Revista: Curr Oncol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Robótica / Procedimentos Cirúrgicos Robóticos Limite: Humans / Male Idioma: En Revista: Curr Oncol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica