Evidence map›Paper›PMID 41746195›Full record

ArticleMedical physics2026

A prescription-free, radiobiology-based framework for automated VMAT planning: A feasibility study in primary prostate cancer radiotherapy.

Dejan Kuhn, Simon K B Spohn, Constantinos Zamboglou, Anca-Ligia Grosu, Dimos Baltas, Ilias Sachpazidis

Abstract read
In one paragraph

Article in Medical physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Dejan KuhnDivision of Medical Physics, Department of Radiation Oncology, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Simon K B SpohnDepartment of Radiation Oncology, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Constantinos ZamboglouDepartment of Radiation Oncology, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Anca-Ligia GrosuDepartment of Radiation Oncology, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Dimos BaltasDivision of Medical Physics, Department of Radiation Oncology, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Ilias SachpazidisDivision of Medical Physics, Department of Radiation Oncology, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.

Funding

Varian Medical Systems, a Siemens Healthineers Company 1353
6 · The paper itself

Abstract

backgroundCurrent VMAT planning workflows for prostate cancer primarily depend on conventional dose-volume criteria specified at discrete dose or volume points. These point-based objectives, however, do not necessarily lead to globally optimal, patient-specific treatment plans. While radiobiological models such as Tumor Control Probability (TCP) and Normal Tissue Complication Probability (NTCP) can provide more meaningful, individualized targets, previous implementations have either employed these for plan evaluation or integrated biological objectives without providing a comprehensive set of deliverable trade-off plans. To date, no prescription-free, automated VMAT planning method has been introduced that generates clinically deliverable, patient-specific Pareto fronts that are biologically interpretable and useful for radiobiological trade-off analysis. PURPOSE: The purpose of this study was to develop and clinically evaluate a fully automated, prescription-free VMAT planning framework for primary prostate cancer that generates Pareto-optimal, clinically deliverable treatment plans in radiobiological objective space, constrained by predefined TCP and NTCP levels.

methodsThe proposed framework was implemented within a commercial treatment planning system (TPS). 17 patients with unfavorable intermediate-risk prostate cancer were retrospectively selected for evaluation. For each patient, TCP and NTCP levels were predefined for three target volumes and seven organs at risk (OARs), restricting the optimization to clinically meaningful regions of the solution space. Plan optimization was performed using Particle Swarm Optimization (PSO) to iteratively adjust VMAT parameters, with the complication-free tumor control probability (P

resultsThe proposed prescription-independent planning approach successfully generated individualized pseudo-Pareto fronts for all 17 patients in the radiobiological space of P

conclusionThis study demonstrated the feasibility of a fully automated, prescription-free VMAT planning framework for primary prostate cancer, indicating its potential for future clinical implementation. The proposed framework directly optimized treatment plans in radiobiological objective space, producing Pareto-optimal, clinically deliverable solutions using predefined TCP and NTCP levels. It enables patient-specific trade-off analysis taking into account tumor control and normal tissue complication risk. The work provides a foundation for further development, including the incorporation of geometric uncertainties, acceleration through parallel or GPU-based computation, and application to additional tumor sites.

Indexed as

Prostatic NeoplasmsRadiobiologyRadiotherapy, Intensity-ModulatedRadiotherapy Planning, Computer-AssistedAutomationFeasibility StudiesHumansMaleOrgans at RiskProbabilityRadiotherapy Dosageautomatic treatment planningbiologically interpreted Pareto analysisnormal tissue complication probability (NTCP)particle swarm optimizaiton (PSO)prescription‐free treatment planningprostate cancer radiotherapyradiobiologically guided treatment planningtumor control probability (TCP)volumetric modulated arc therapy (VMAT)

Identifiers

PMID41746195
PMCPMC12940459

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.