Show simple item record

dc.contributor.authorChen, K.
dc.contributor.authorHou, L.
dc.contributor.authorChen, M.
dc.contributor.authorLi, S.
dc.contributor.authorShi, Y.
dc.contributor.authorRaynor, W.Y.
dc.contributor.authorYang, H.
dc.date.accessioned2024-08-07T19:42:19Z
dc.date.available2024-08-07T19:42:19Z
dc.date.issued2023-03-27
dc.identifier.citationChen, K.; Hou, L.; Chen, M.; Li, S.; Shi, Y.; Raynor, W.Y.; Yang, H. Predicting the Efficacy of SBRT for Lung Cancer with 18F-FDG PET/CT Radiogenomics. Life 2023, 13, 884. https://doi.org/10.3390/life13040884
dc.identifier.issn2075-1729
dc.identifier.doi10.3390/life13040884
dc.identifier.urihttp://hdl.handle.net/10150/673935
dc.description.abstractPurpose: to develop a radiogenomic model on the basis of 18F-FDG PET/CT radiomics and clinical-parameter EGFR for predicting PFS stratification in lung-cancer patients after SBRT treatment. Methods: A total of 123 patients with lung cancer who had undergone 18F-FDG PET/CT examination before SBRT from September 2014 to December 2021 were retrospectively analyzed. All patients’ PET/CT images were manually segmented, and the radiomic features were extracted. LASSO regression was used to select radiomic features. Logistic regression analysis was used to screen clinical features to establish the clinical EGFR model, and a radiogenomic model was constructed by combining radiomics and clinical EGFR. We used the receiver operating characteristic curve and calibration curve to assess the efficacy of the models. The decision curve and influence curve analysis were used to evaluate the clinical value of the models. The bootstrap method was used to validate the radiogenomic model, and the mean AUC was calculated to assess the model. Results: A total of 2042 radiomics features were extracted. Five radiomic features were related to the PFS stratification of lung-cancer patients with SBRT. T-stage and overall stages (TNM) were independent factors for predicting PFS stratification. AUCs under the ROC curve of the radiomics, clinical EGFR, and radiogenomic models were 0.84, 0.67, and 0.86, respectively. The calibration curve shows that the predicted value of the radiogenomic model was in good agreement with the actual value. The decision and influence curve showed that the model had high clinical application values. After Bootstrap validation, the mean AUC of the radiogenomic model was 0.850(95%CI 0.849–0.851). Conclusions: The radiogenomic model based on 18F-FDG PET/CT radiomics and clinical EGFR has good application value in predicting the PFS stratification of lung-cancer patients after SBRT treatment. © 2023 by the authors.
dc.language.isoen
dc.publisherMDPI
dc.rights© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject<sup>18</sup>F-fluorodeoxyglucose positron emission tomography/computed tomography
dc.subjectepidermal growth factor receptor
dc.subjectlung cancer
dc.subjectradiogenomics
dc.subjectstereotactic body radiation therapy
dc.titlePredicting the Efficacy of SBRT for Lung Cancer with 18F-FDG PET/CT Radiogenomics
dc.typeArticle
dc.typetext
dc.contributor.departmentDepartment of Radiation Oncology, University of Arizona
dc.identifier.journalLife
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal Published Version
dc.source.journaltitleLife
refterms.dateFOA2024-08-07T19:42:19Z


Files in this item

Thumbnail
Name:
life-13-00884.pdf
Size:
3.211Mb
Format:
PDF
Description:
Final Published Version

This item appears in the following Collection(s)

Show simple item record

© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Except where otherwise noted, this item's license is described as © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.