ArticleFrontiers in oncology2024
Development and validation of a lung biological equivalent dose-based multiregional radiomic model for predicting symptomatic radiation pneumonitis after SBRT in lung cancer patients.
Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.
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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.
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Who cites it
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
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Authors and funding
9 authors.
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Abstract
Background: This study aimed to develop and validate a multiregional radiomic-based composite model to predict symptomatic radiation pneumonitis (SRP) in non-small cell lung cancer (NSCLC) patients treated with stereotactic body radiation therapy (SBRT). Materials and methods: 189 patients from two institutions were allocated into training, internal validation and external testing cohorts. The associations between the SRP and clinic-dosimetric factors were analyzed using univariate and multivariate regression. Radiomics features were extracted from seven discrete and three composite regions of interest (ROIs), including anatomical, physical dosimetry, and biologically equivalent dose (BED) dimensions. Correlation filters and Lasso regularization were applied for feature selection and five machine learning algorithms were utilized to construct radiomic models. Multiregional radiomic models integrating features from various regions were developed and undergone performance test in comparison with single-region models. Ultimately, three models-a radiomic model, a dosimetric model, and a combined model-were developed and evaluated using receiver operating characteristic (ROC) curve, model calibration, and decision curve analysis. Results: V Conclusions: The combined model improves SRP prediction across various SBRT fractionation schemes, which warrants further validation and optimization using larger-scale retrospective data and in prospective trials.
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