ArticlePhysical and engineering sciences in medicine2026
Predicting VMAT patient-specific quality assurance outcome using a machine learning workflow.
Article in Physical and engineering sciences in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
- Erratum issued
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
To develop a machine learning (ML)-based workflow for virtual patient-specific quality assurance (PSQA) to predict local gamma passing rates (GPRs) and QA pass/fail outcomes for Volumetric Modulated Arc Therapy (VMAT) plans. Treatment plan files from 156 double-arc VMAT cases were used, resulting in 312 beam-specific datasets. A total of 48 plan complexity metrics (PCMs), derived from DICOM RT plan files based on the UCoMX framework, were calculated for each arc. Feature selection was performed using a blended ensemble of Random Forest (RF), Gradient Boosting Decision Tree (GBDT), eXtreme Gradient Boost (XGBoost), and linear Support Vector Machine (SVM) models, yielding 15 key predictive features. Regression models using RF, GBDT, XGBoost, SVR, and an averaging ensemble were trained to predict local GPR values. Patient-level grouped train-test splitting and grouped 5-fold cross-validation were employed to prevent data leakage. Classification models were developed using a 90% GPR threshold to predict QA pass/fail outcomes. Model performance was evaluated using Mean Absolute Error (MAE), Root Mean Square Error (RMSE), ROC-AUC, sensitivity, specificity, Positive Predictive Value (PPV), and Negative Predictive Value (NPV). Among the regression models, GBDT achieved the best overall performance with an MAE of 1.85% points and an RMSE of 2.35% points, followed closely by the averaging ensemble model. Grouped 5-fold cross-validation demonstrated stable regression performance across all models. For classification analysis, grouped 5-fold cross-validation ROC-AUC values ranged from 0.721 to 0.772, with SVM achieving the highest mean cross-validation ROC-AUC. On the independent test dataset, SVM achieved the highest ROC-AUC (0.725) and specificity (0.829), while the averaging ensemble model demonstrated balanced classification performance with improved specificity and PPV. An ML-based workflow for predicting VMAT PSQA outcomes from plan complexity metrics derived from DICOM RT plans has been developed. The results demonstrate the feasibility of predicting QA outcomes with moderate accuracy and provide a framework for further development of ML-assisted PSQA. Future studies incorporating additional plan, delivery, and machine-related features, together with larger multi-institutional datasets, may further improve predictive performance and clinical applicability.
Indexed as
Identifiers
42658407What OpenQuestion holds
Registered trials
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.