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Sensitivity analysis of dose-response model parameters for the bladder in prostate cancer radiotherapy

  • Tanuj Puri*
  • , Tiziana Rancati
  • , Petra Seibold
  • , Adam Webb
  • , Eliana Vasquez osorio
  • , David Azria
  • , Marie-Pierre Farcy-Jacquet
  • , Jenny Chang-Claude
  • , Alison Dunning
  • , Maarten Lambrecht
  • , Barbara Avuzzi
  • , Dirk de Ruysscher
  • , Elena Sperk
  • , Ana Vega
  • , Liv Veldeman
  • , Barry Rosenstein
  • , Sarah Kerns
  • , Christopher Talbot
  • , Alan McWilliam
  • , Peter Hoskin
  • Ananya Choudhury, Catharine West, Marcel van Herk
*Corresponding author for this work
  • University of Manchester
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • German Cancer Research Center
  • University of Leicester
  • Centre régional de lutte du cancer Val d'Aurelle
  • CHU de Nîmes
  • University of Cambridge
  • KU Leuven
  • Maastricht University
  • Heidelberg University 
  • Instituto de Investigación Sanitaria de Santiago de Compostela
  • Fundación Pública Galega de Medicina Xenómica
  • Ghent University
  • Icahn School of Medicine at Mount Sinai
  • Medical College of Wisconsin

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Introduction: This study evaluates how model parameter values affect dose–response maps (DRMs) in identifying high-risk bladder subregions associated with late urinary toxicities in prostate cancer patients post-radiotherapy. Methods: Data from 1808 patients were analyzed for five late bladder toxicities. Baseline scores were subtracted from maximum toxicity at 12 and 24 months and dichotomized into grades ≥ 1 and ≥ 2. Bladders were segmented on computed tomography scans, and dose-surface maps (DSMs) were created on 91 × 90 voxel grids using spherical and cylindrical coordinates. Voxel doses were converted to equivalent dose in 2 Gy fractions (EQD2, α/β 1–3 Gy). Welch's t and Mann–Whitney U equations were applied at each voxel location. Multiple comparisons were corrected via permutation testing (10–10000 iterations), and statistically significant voxels were identified using the 90th and 95th percentiles of Tmax/Umax. Sensitivity of parameters was assessed by varying one parameter at a time, with changes > 400 voxels (∼5% of 8190) classified as large and ≤ 400 as small. Results: Urinary tract obstruction was the only toxicity significantly associated with bladder DSMs, focusing results on this outcome. After baseline adjustment and dichotomization, event/nonevent counts were 62/701 (grade≥1) and 21/742 (grade≥2; N = 763). DRM results showed large effects of toxicity grade threshold, coordinate system, statistical test equation, and Tmax/Umax thresholding. EQD2 α/β showed variable effects, large for cylindrical and small for spherical coordinates, while the number of permutations had only a small effect. Conclusions: Parameter selection significantly influences high-risk subregion identification in DRMs, emphasizing the need for standardized parameter reporting for meaningful external comparisons.
Original languageEnglish
Article number105178
JournalPhysica medica
Volume139
DOIs
Publication statusPublished - 1 Nov 2025

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

  • Bladder
  • IBDM
  • Image-based data mining
  • Imaging biomarker
  • Multicenter clinical trial
  • OAR
  • Organ-at-risk
  • Prediction model
  • Predictive modeling
  • Prostate cancer
  • Radiotherapy
  • Standardization
  • Toxicity
  • VBA
  • Voxel-based dose–response analysis

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