Evidence map›Paper›PMID 42638300›Full record

ArticleJournal of applied clinical medical physics2026

A rule-based, feedback-driven framework for fully automated prostate VMAT planning.

Joel Sangster, Megan Taylor, David Jolly, Jerome Gastaldo, Friedlieb Lorenz

Abstract read
In one paragraph

Article in Journal of applied clinical 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Joel SangsterDepartment of Radiation Oncology, St George's Cancer Care Centre, Christchurch, Canterbury, New Zealand.
Megan TaylorDepartment of Radiation Oncology, St George's Cancer Care Centre, Christchurch, Canterbury, New Zealand.
David JollyDepartment of Radiation Oncology, St George's Cancer Care Centre, Christchurch, Canterbury, New Zealand.
Jerome GastaldoDepartment of Radiation Oncology, St George's Cancer Care Centre, Christchurch, Canterbury, New Zealand.
Friedlieb LorenzDepartment of Radiation Oncology, St George's Cancer Care Centre, Christchurch, Canterbury, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundManual prostate volumetric modulated arc therapy (VMAT) planning in Elekta Monaco is complex, time-intensive, and prone to planner variability. Existing automation methods, such as knowledge-based planning (KBP) and cloud-based solutions often rely on external models rather than Monaco's native optimization. A treatment planning system (TPS)-integrated, feedback-driven approach could improve consistency and transparency while maintaining clinical quality. PURPOSE: To develop and validate a fully automated planning algorithm (APA) that actively interacts with Monaco via its application programming interface (API), mimicking expert user behavior during optimization to deliver consistent, high-quality plans.

methodsThe APA was developed as a rule-based, fully deterministic workflow within the Monaco TPS, leveraging its native constrained and multicriterial optimization framework to enable end-to-end automated VMAT prostate plan generation. A retrospective, paired dosimetric study was conducted on localized prostate cancer cases. For each patient, the clinically approved manual plan was compared to an automated plan generated by the APA. The workflow reads target and organ-at-risk (OAR) objectives from the plan, monitors Monaco's optimization feedback-including dose-volume histogram (DVH) metrics and cost-function weights-and iteratively adjusts objectives. Endpoints included target coverage, OAR dose metrics, complexity, conformity, and planning time.

resultsAutomated plans achieved non-inferior target coverage with a median difference in PTV V57 Gy of -0.275% (p = 0.116) between automated and manual plans. Automated plans produced statistically significant reductions in intermediate and low rectal doses including V40 Gy (1.62%, p = 0.003), V32 Gy (4.28%, p < 0.001), and V24 Gy (8.19%, p < 0.001), while high rectal doses (48-60 Gy) showed no statistically significant differences (p > 0.05). Similarly for the bladder, automated plans significantly reduced V48 Gy (4.07%, p < 0.001) and V40 Gy (2.91%, p < 0.001), with a modest increase in high dose bladder volume (V60 Gy +1.33%, p < 0.001). Mean execution time for automated plans was 38.7 ± 14.7 min per case, compared to an informally estimated manual planning time of 2 h at our institution. All automated plans met institutional clinical acceptability criteria.

conclusionsA TPS-native, feedback-driven automation using the Monaco Scripting API can replicate clinical planning strategies without human intervention, eliminating user variability and improving consistency. This approach offers a practical pathway for high-quality prostate VMAT planning in routine clinical practice.

Indexed as

AlgorithmsOrgans at RiskProstatic NeoplasmsRadiotherapy, Intensity-ModulatedRadiotherapy Planning, Computer-AssistedAutomationFeedbackHumansMaleRadiotherapy DosageRetrospective Studiesautomationmonacoprostate

Identifiers

PMID42638300
PMCPMC13504152

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