Using machine learning to predict treatment delivery accuracy in brain stereotactic radiosurgery.

L Lian Duan (Key Lab of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry) M Mallory C. Glenn (The University of Texas MD Anderson Cancer Center, Houston, TX) P Paige Taylor (The University of Texas MD Anderson Cancer Center, Houston, TX) C Clifton Dave Fuller (The University of Texas MD Anderson Cancer Center, Houston, TX) V Vanessa Panettieri (Peter MacCallum Cancer Centre, Melbourne, Australia) C Christine Peterson H Hunter S. Mehrens (The University of Texas MD Anderson Cancer Center, Houston, TX) M Michael Yang (The University of Texas MD Anderson Cancer Center, Houston, TX) D Derek M. Garcia (The University of Texas MD Anderson Cancer Center, Houston, TX) S Stephen F. Kry (The University of Texas MD Anderson Cancer Center, Houston, TX)

Abstract

e14007 Background: Accurate dose delivery in SRS is critical when treating small intracranial targets near critical structures. Suboptimal delivery can impact patient outcomes and have the potential to compromise clinical trial results. The SRS Head Phantom, issued by the Radiation Quality Assurance Lab (IROC) is a standardized patient surrogate used as a mandatory credentialing tool for institutions participating in NCI-sponsored clinical trials involving SRS. This study aims to develop ML models capable of predicting SRS delivery accuracy across various platforms and clinical settings. This approach can help identify key factors associated with suboptimal performance and could supplement the physical process to streamline clinical trial credentialing. Methods: We analyzed 930 SRS audit results from 673 institutions participating in the RQALab/IROC program between 2013 and 2023. The phantom contains a 1.9 cm spherical target with embedded detectors. Each test evaluated delivered versus intended dose at the treatment target, requiring agreement within ±5%3mm. We collected 60 features encompassing treatment and planning parameters, plan quality indices, and measures of plan complexity and used these to predict delivery accuracy. Random Forest models were trained to predict dose delivery deviation and pass/fail status. The dataset was divided into seven subgroups based on machine type and treatment planning system. Within each group, models were trained using a 25x4-fold cross-validation approach. SHAP (SHapley Additive exPlanations) values were utilized to identify the top contributing features and ensure model interpretability. Results: Machine-learning models predicted the delivered target dose with a mean absolute error of 2% in the largest practice cohort (N=320). For predicting unacceptable deliveries, the models exhibited high sensitivity (98%) and accuracy (0.93). For dedicated Gamma Knife platforms (N=77), the models achieved 99% prediction accuracy. Interpretability analyses revealed that plan quality metrics were the dominant predictors of suboptimal delivery accuracy; specifically, poor plan quality correlated with larger deviations between planned and delivered doses. Conformity and dose gradient were identified as top contributors across most cohorts. The specific ranking and predictive weight of these features varied by modality; for instance, complexity metrics contributed significantly to modulated plans, whereas target volume metrics played a larger role in deliveries using dedicated SRS treatment machines. Conclusions: Machine learning can effectively identify SRS deliveries at risk of failure through models tailored to specific delivery modalities. By integrating explainable AI methods, this approach highlights actionable strategies to improve precision, standardize performance across institutions, and enhance patient safety.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

L

Lian Duan

Key Lab of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry

M

Mallory C. Glenn

The University of Texas MD Anderson Cancer Center, Houston, TX

P

Paige Taylor

The University of Texas MD Anderson Cancer Center, Houston, TX

C

Clifton Dave Fuller

The University of Texas MD Anderson Cancer Center, Houston, TX

V

Vanessa Panettieri

Peter MacCallum Cancer Centre, Melbourne, Australia

C

Christine Peterson

H

Hunter S. Mehrens

The University of Texas MD Anderson Cancer Center, Houston, TX

M

Michael Yang

The University of Texas MD Anderson Cancer Center, Houston, TX

D

Derek M. Garcia

The University of Texas MD Anderson Cancer Center, Houston, TX

S

Stephen F. Kry

The University of Texas MD Anderson Cancer Center, Houston, TX