Evidence map›Paper›PMID 40690180›Full record

ArticlePhysical and engineering sciences in medicine2025

Evaluating Monaco 6.2.2 in complex radiotherapy across matched LINACs: improved MLC modelling and dose accuracy with virtual source model 2.0.

Luis Muñoz, Peter McLoone, Peter Metcalfe, Anatoly B Rosenfeld, Giordano Biasi

Abstract readEvaluation Study
In one paragraph

Article in Physical and engineering sciences in medicine, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Luis MuñozGenesiscare Flinders Private Hospital, Bedford Park, SA, Australia. luis.munoz@genesiscare.com.ORCID http://orcid.org/0000-0003-3605-3457
Peter McLooneSouth Western Sydney Local Health District, Liverpool, NSW, Australia.
Peter MetcalfeCentre for Medical Radiation Physics, University of Wollongong, Wollongong, NSW, Australia.
Anatoly B RosenfeldCentre for Medical Radiation Physics, University of Wollongong, Wollongong, NSW, Australia.
Giordano BiasiCentre for Medical Radiation Physics, University of Wollongong, Wollongong, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study assesses the updated Monaco TPS virtual source model (VSM) 2.0, which removes multileaf collimator (MLC) and jaw characterization as editable factors from the MLC geometry section within Monaco. The focus is on the impact of changes to stereotactic radiotherapy (SRT) cases for spinal and intracranial treatments for two beam matched linear accelerators. A validated custom VSM 1.6 model optimized for SRT was compared with the Elekta Accelerated Go Live 6 MV flattening filter-free (FFF) and VSM 2.0. Evaluations included measured MLC characteristics with a high-resolution detector, measured output factors (OPF), ion chamber fields in the thorax phantom, and recalculations of clinically relevant SRT cases. VSM 2.0 improves MLC modelling. Ion chamber measurements for IAEA TD1583 measurements were found to be within expected tolerances. Gamma pass rates for two matched LINACs evidenced improvement at 1%, 1 mm and 10% threshold for single and multi-SRS brain and SABR Spine treatments. VSM 2.0 represents a meaningful advancement in beam modelling within a Monte Carlo-based TPS environment, offering improved dosimetric performance and operational simplicity. Commercially available detectors were used to demonstrate that VSM 2.0 enhances agility MLC modelling, supporting more precise SRT and SABR delivery for matched LINACs. Removing configurable dependencies from the beam model will result in more consistent high quality beam models, an improves workflows for commissioning of the Monaco TPS.

Indexed as

Radiotherapy Planning, Computer-AssistedHumansMonte Carlo MethodParticle AcceleratorsCharacterisationMLCModellingSIMTSpineSRT

Identifiers

PMID40690180
PMCPMC12738645

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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.