Logo Logo
Switch Language to German

Fossati, Nicola; Suardi, Nazareno; Gandaglia, Giorgio; Bravi, Carlo A.; Soligo, Matteo; Karnes, R. Jeffrey; Shariat, Shahrokh; Battaglia, Antonino; Everaerts, Wouter; Joniau, Steven; van Poppel, Hendrik; Rajarubendra, Nieroshan; Gill, Inderbir S.; Larcher, Alessandro; Mottrie, Alexander; Schmautz, Maximilian; Heidenreich, Axel; Kalz, Almut; Osmonov, Daniar; Juenemann, Klaus-Peter; Herlemann, Annika; Gratzke, Christian; Stief, Christian; Montorsi, Francesco and Briganti, Alberto (2019): Identifying the Optimal Candidate for Salvage Lymph Node Dissection for Nodal Recurrence of Prostate Cancer: Results from a Large, Multi-institutional Analysis. In: European Urology, Vol. 75, No. 1: pp. 176-183

Full text not available from 'Open Access LMU'.


Background: Salvage lymph node dissection (SLND) represents a possible treatment option for prostate cancer patients affected by nodal recurrence after local treatment. However, SLND may be associated with intra-and postoperative complications, and the oncological benefit may be limited to specific groups of patients. Objective: To identify the optimal candidates for SLND based on preoperative characteristics. Design, setting, and participants: The study included 654 patients who experienced prostate-specific antigen (PSA) rise and nodal recurrence after radical prostatectomy (RP) and underwent SLND at nine tertiary referral centers. Lymph node recurrence was documented by positron emission tomography/computed tomography (PET/CT) scan using either C-11-choline or Ga-68-labeled prostate-specific membrane antigen ligand. Intervention: SLND. Outcome measurements and statistical analysis: The study outcome was early clinical recurrence (eCR) developed within 1 yr after SLND. Multivariable Cox regression analysis was used to develop a predictive model. Multivariable-derived coefficients were used to develop a novel risk calculator. Decision-curve analysis was used to evaluate the net benefit of the predictive model. Results and limitations: Median follow-up was 30 (interquartile range, 16-50) mo among patients without clinical recurrence (CR), and 334 patients developed CR after SLND. In particular, eCR at 1 yr after SLND was observed in 150 patients, with a Kaplan-Meier probability of eCR equal to 25%. The development of eCR was significantly associated with an increased risk of cancer-specific mortality at 3 yr, being 20% versus 1.4% in patients with and without eCR, respectively (p < 0.0001). At multivariable analysis, Gleason grade group 5 (hazard ratio [HR]: 2.04;p < 0.0001), time from RP to PSA rising (HR: 0.99;p = 0.025), hormonal therapy administration at PSA rising after RP (HR: 1.47;p = 0.0005), retroperitoneal uptake at PET/CT scan (HR: 1.24;p = 0.038), three or more positive spots at PET/CT scan (HR: 1.26;p = 0.019), and PSA level at SLND (HR: 1.05;p < 0.0001) were significant predictors of CR after SLND. The coefficients of the predictive model were used to develop a risk calculator for eCR at 1 yr after SLND. The discrimination of the model (Harrel's C index) was 0.75. At decision-curve analysis, the net benefit of the model was higher than the "treat-all" option at all the threshold probabilities. Conclusions: We reported the largest available series of patients treated with SLND. Roughly 25% of men developed eCR after surgery. We developed the first risk stratification tool to identify the optimal candidate to SLND based on routinely available preoperative characteristics. This tool can be useful to avoid use of SLND in men more likely to progress despite any imaging-guided approach. Patient summary: The risk of early recurrence after salvage lymph node dissection (SLND) was approximately 25%. In this study, we developed a novel tool to predict the risk of early failure after SLND. This tool will be useful to identify patients who would benefit the most from SLND from other patients who should be spared from surgery. (C) 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Actions (login required)

View Item View Item