Ultra-hypofractionated radiotherapy with focal boost for high-risk localized prostate cancer (HYPO-RT-PC-boost): in silico evaluation with histological reference
DOI:
https://doi.org/10.2340/1651-226X.2025.44211Keywords:
In silico, Radiotherapy, focal boosting, Prostate cancer, hypofractionationAbstract
Background and purpose: The study aims to evaluate dosimetric properties of hypofractionated treatment plans integrating focal boost, using registered whole-mount histopathology (WMHP) as reference standard.
Methods: Fifteen men from the PAMP trial (EudraCT: 2015-005046-55) were included. Participants had ≥ 1 ISUP Grade group ≥ 4 lesion and underwent [68Ga]prostate-specific membrane antigen (PSMA) positron emission tomography/multiparametric magnetic resonance imaging (PET/mpMRI) and [11C]Acetate-PET/computed tomography before radical prostatectomy. Four radiation oncologists delineated gross tumor volumes (GTVs) on PSMA-PET/mpMRI. Sixty treatment plans were optimized, one per GTV and patient. Prostate planning target volumes were prescribed 42.7 Gy in seven fractions, with a simultaneous GTV boost up to 49.0 Gy, prioritizing organs at risk (OARs). Digital WMHP provided Gleason grading and was co-registered with in-vivo imaging. Target coverage for GTVs and voxels sharing Gleason patterns (GPs) was assessed via dose-volume histogram (DVH) analysis. Interobserver agreement in GTV-delineations was quantified with Fleiss’ kappa.
Results: The median GTV dose per plan (D50) ranged from 48.3 to 49.1 Gy. For voxels with the highest GP, D50 was 42.9–49.2 Gy, exceeding 47.2 Gy in all except one plan. In lowest pattern voxels, D50 was 42.5–49.3 Gy, and below 43.4 Gy in over half the plans. Significant positive correlations between Fleiss’ kappa and DVH parameters appeared only for GP 5 regions, specifically for Fleiss’ kappa and D50 for two observers and the average D50 across observers.
Interpretation: The histologically confirmed tumor was only partially boosted. Regions with more aggressive disease received better coverage. These findings provide a rational for prioritizing OARs in treatment planning.
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Copyright (c) 2025 Erik Nilsson, Anneli Nilsson, Joakim Jonsson, Kristina Sandgren, Josefine Grefve, Jan Axelsson, Angsana K. Lindberg, Karin Söderkvist, Camilla T. Karlsson, Björn Zackrisson, Sara Strandberg, Katrine Riklund, Anders Bergh, Mathieu Moreau, Adalsteinn Gunnlaugsson, Lars E. Olsson, Tufve Nyholm

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