{"title":"Long-term prediction of radiation-induced optic neuropathy: A mixed-effects analysis of visual field kinetics following proton therapy","authors":"Thao-Nguyen Pham , Thibaud Mathis , Nathan Azemar , Anthony Vela , Jean-Claude Quintyn , Juliette Thariat","doi":"10.1016/j.radonc.2025.111205","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Radiation-induced optic neuropathy (RION) is a rare but serious complication of radiotherapy, leading to progressive vision loss. The temporal dynamics of RION are poorly understood, limiting effective monitoring and intervention. We developed a predictive mixed-effects model of visual field deterioration, a sensitive surrogate marker for clinically-reported RION, by integrating longitudinal clinical and dosimetric data, to anticipate long-term visual outcomes.</div></div><div><h3>Methods</h3><div>Out of a prospective database of 238 patients, 179 eyes from 105 patients treated with pencil beam scanning proton therapy were included. All selected eyes had no significant visual field deficit at baseline, defined as a mean visual sensitivity loss better than −6 dB. Baseline clinical characteristics, detailed dosimetric data, and longitudinal visual field assessments were collected. Temporal changes in mean visual sensitivity were analyzed using feature selection through random forest models and linear regression. A nonlinear mixed-effects model was then developed to predict the trajectory of visual field deterioration over time.</div></div><div><h3>Results</h3><div>Visual field deterioration progressed significantly over time, with a quadratic model best capturing the kinetics. Mean sensitivity loss accelerated with increasing age and clinical target volume. Incorporating the full dose-volume histogram, the volume of the optic chiasma received at least 40 Gy (V<sub>40</sub>/chiasma), improved model performance. Simulation based on this model showed that the probability of RION increased sharply over time: 4.6 % at 2 years, and 28.3 % at 5 years.</div></div><div><h3>Conclusion</h3><div>This model confirms and expands upon prior work by showing that clinical factors can outweigh dosimetric ones in predicting RION progression. Our model was capable of predicting long-term visual outcomes even in patients with limited follow-up.</div></div>","PeriodicalId":21041,"journal":{"name":"Radiotherapy and Oncology","volume":"213 ","pages":"Article 111205"},"PeriodicalIF":5.3000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiotherapy and Oncology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167814025052090","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction
Radiation-induced optic neuropathy (RION) is a rare but serious complication of radiotherapy, leading to progressive vision loss. The temporal dynamics of RION are poorly understood, limiting effective monitoring and intervention. We developed a predictive mixed-effects model of visual field deterioration, a sensitive surrogate marker for clinically-reported RION, by integrating longitudinal clinical and dosimetric data, to anticipate long-term visual outcomes.
Methods
Out of a prospective database of 238 patients, 179 eyes from 105 patients treated with pencil beam scanning proton therapy were included. All selected eyes had no significant visual field deficit at baseline, defined as a mean visual sensitivity loss better than −6 dB. Baseline clinical characteristics, detailed dosimetric data, and longitudinal visual field assessments were collected. Temporal changes in mean visual sensitivity were analyzed using feature selection through random forest models and linear regression. A nonlinear mixed-effects model was then developed to predict the trajectory of visual field deterioration over time.
Results
Visual field deterioration progressed significantly over time, with a quadratic model best capturing the kinetics. Mean sensitivity loss accelerated with increasing age and clinical target volume. Incorporating the full dose-volume histogram, the volume of the optic chiasma received at least 40 Gy (V40/chiasma), improved model performance. Simulation based on this model showed that the probability of RION increased sharply over time: 4.6 % at 2 years, and 28.3 % at 5 years.
Conclusion
This model confirms and expands upon prior work by showing that clinical factors can outweigh dosimetric ones in predicting RION progression. Our model was capable of predicting long-term visual outcomes even in patients with limited follow-up.
期刊介绍:
Radiotherapy and Oncology publishes papers describing original research as well as review articles. It covers areas of interest relating to radiation oncology. This includes: clinical radiotherapy, combined modality treatment, translational studies, epidemiological outcomes, imaging, dosimetry, and radiation therapy planning, experimental work in radiobiology, chemobiology, hyperthermia and tumour biology, as well as data science in radiation oncology and physics aspects relevant to oncology.Papers on more general aspects of interest to the radiation oncologist including chemotherapy, surgery and immunology are also published.