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Intermediate clinical endpoints as surrogates for overall survival after salvage prostatectomy

  • Navid Roessler*
  • , Zuzanna Nowicka
  • , Marcin Miszczyk
  • , Giorgio Calleris
  • , Alessandro Dematteis
  • , Malte W. Vetterlein
  • , Simone Albisinni
  • , Henk G. van der Poel
  • , Paul Cathcart
  • , Giovanni E. Cacciamani
  • , Inderbir S. Gill
  • , Raj A. Persad
  • , Steven Joniau
  • , Rafael Sanchez-Salas
  • , Joseph A. Smith
  • , Robert Jeffrey Karnes
  • , Mohamed E. Ahmed
  • , Pawel Rajwa
  • , Derya Tilki
  • , the Young Academic Urologists Prostate Cancer Working Party
  • *Corresponding author for this work
  • Medical University of Vienna
  • University of Hamburg
  • Medical University of Łódź
  • WSB University
  • University of Turin
  • Université libre de Bruxelles
  • Antoni van Leeuwenhoek Hospital
  • Guy's and St Thomas' NHS Foundation Trust
  • University of Southern California
  • Bristol Urological Institute
  • KU Leuven
  • Institut mutualiste Montsouris
  • Vanderbilt University
  • Mayo Clinic Rochester, MN
  • Medical University of Silesia in Katowice
  • Koc University
  • Cornell University
  • University of Texas Southwestern Medical Center
  • Charles University
  • Al Ahliyya Amman University
  • Karl Landsteiner Institute of Urology and Andrology

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

Objectives: To evaluate biochemical recurrence-free survival (BRFS) and metastasis-free survival (MFS) as potential intermediate clinical endpoints (ICEs) for overall survival (OS) in patients undergoing salvage radical prostatectomy (sRP). Patients and Methods: Evaluable patients were selected from a retrospective dataset, resulting in a cohort of 879 patients with recurrent, non-metastatic, hormone-sensitive prostate cancer treated with sRP at 13 centres. ICE surrogacy was evaluated using a two-stage approach: (i) at the individual-patient level by fitting Clayton copula models and estimating Kendall's (Formula presented.) ((Formula presented.) >0.7 indicating a strong association) and (ii) at the centre level, by fitting weighted linear regression of 5-year OS on 3-year BRFS and MFS. Results: The two-step analysis included 759 patients for BRFS (366 events) and 476 for MFS (137 events), with median follow-up of 37 months (95% confidence interval [CI] 36–42 months) and 34 months (95% CI 31–37 months), respectively. At the individual-patient level, MFS showed a strong association with OS (Kendall's (Formula presented.) 0.85, 95% CI 0.82–0.88), which was not observed for BRFS (Kendall's (Formula presented.) 0.63, 95% CI 0.56–0.69). At the centre level, neither 3-year BRFS (R2 = 0.15; slope = 0.34, P = 0.2) nor 3-year MFS (R2 = 0.21; slope = 0.26, P = 0.14) predicted 5-year OS with sufficient explanatory power. Limitations include the fact that centre-level analysis was based on single-arm associations rather than on treatment-effect surrogacy across arms, and retrospective data collection. Conclusions: The BRFS should not be used as a surrogate endpoint in the sRP setting. MFS requires further validation in future prospective studies to confirm its association with OS. Patient-reported outcomes, such as quality-of-life and treatment-related toxicity, should be considered in parallel with OS.
Original languageEnglish
Pages (from-to)430-437
Number of pages8
JournalBJU international
Volume138
Issue number3
Early online date2026
DOIs
Publication statusPublished - Sept 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • biochemical recurrence-free survival
  • intermediate clinical endpoint
  • metastasis-free survival
  • salvage radical prostatectomy
  • surrogate endpoints

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