Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117505
PIRA download icon_1.1View/Download Full Text
DC FieldValueLanguage
dc.contributorDepartment of Health Technology and Informatics-
dc.creatorNi, Y-
dc.creatorLee, HFV-
dc.creatorChiang, CL-
dc.creatorCheung, LYA-
dc.creatorHuang, Z-
dc.creatorTeng, X-
dc.creatorZhang, J-
dc.creatorRen, G-
dc.creatorCai, J-
dc.creatorLi, T-
dc.date.accessioned2026-02-26T03:46:23Z-
dc.date.available2026-02-26T03:46:23Z-
dc.identifier.urihttp://hdl.handle.net/10397/117505-
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.rights© 2025 The Author(s). Published by Elsevier Inc. on behalf of American Society for Radiation Oncology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Ni, Y., Lee, H.-F. V., Chiang, C.-l., Cheung, L.-Y. A., Huang, Z., Teng, X., Zhang, J., Ren, G., Cai, J., & Li, T. (2025). Functional Dose-Volume Analysis Based on a Novel Image Biomarker Derived From Dynamic Contrast-Enhanced Magnetic Resonance Imaging for Predicting Poststereotactic Body Radiation Therapy Liver Function Preservation in Patients With Hepatocellular Carcinoma. Advances in Radiation Oncology, 10(11), 101883 is available at https://doi.org/10.1016/j.adro.2025.101883.en_US
dc.titleFunctional dose-volume analysis based on a novel image biomarker derived from dynamic contrast-enhanced magnetic resonance imaging for predicting poststereotactic body radiation therapy liver function preservation in patients with hepatocellular carcinomaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume10-
dc.identifier.issue11-
dc.identifier.doi10.1016/j.adro.2025.101883-
dcterms.abstractPurpose: The purpose of this study is to identify functional dose-volume parameters based on image biomarker derived from dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) for predicting poststereotactic body radiation therapy (SBRT) liver function deterioration (LFD) in patients with hepatocellular carcinoma.-
dcterms.abstractMethods and Materials: Forty-eight patients treated with SBRT were retrospectively included. All patients underwent gadoxetate-enhanced DCE-MRI before treatment. Equivalent uniform dose, absolute dose-volume parameters including Dxcc and VxGy(cc) were calculated in 3 liver volumes: the anatomic volume (AV), the high-functional volumes (HFV) defined based on DCE-MRI derived function map, and the low-functional volume (LFV = AV – HFV). The primary endpoint of this study was the LFD as indicated by ∆albumin-bilirubin ≥ 0.5 at 1-month post-SBRT. Dose-volume parameters in patients with and without LFD were compared. Univariate logistic regression models were built to assess the ability of dose-volume parameters to distinguish between LFD and non-LFD cases.-
dcterms.abstractResults: Of the 48 patients, 12 (25%) had LFD (∆albumin-bilirubin ≥ 0.5). The dose-volume parameters in the AV and LFV were not statistically different in patients with and without LFD (P > .005), while D300cc, D400cc, and V10Gy(cc) of the HFV were significantly higher in patients with LFD than in the non-LFD group (P < .005). For distinguishing LFD and non-LFD cases, the mean area under curves (AUCs) for D300cc of AV, LFV, and HFV are 0.60, 0.50, and 0.78, respectively. The mean AUCs for D400cc of AV, LFV, and HFV are 0.62, 0.50, and 0.78, respectively. The mean AUCs for V10Gy of AV, LFV, and HFV are 0.63, 0.48, and 0.77, respectively.-
dcterms.abstractConclusions: The dose-volume parameters derived from HFV were linked to the risk of post-SBRT LFD. These functional parameters derived based on DCE-MRI could be useful to guide more personalized SBRT planning to protect liver function.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOphthalmology science, Nov. 2025, v. 10, no. 11, 101883-
dcterms.isPartOfOphthalmology science-
dcterms.issued2025-11-
dc.identifier.scopus2-s2.0-105018331015-
dc.identifier.eissn2666-9145-
dc.identifier.artn101883-
dc.description.validate202602 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis research was supported by the National Natural Science Foundation of China Young Scientist Fund (NSFC-YSF 82202941), the Innovation and Technology Support Programme (ITS/049/22FP), the research grants of General Research Fund (GRF 15104822, GRF 15102219), Health and Medical Research Fund (HMRF 10211606, HMRF 06173276), and the Research Project Grant of the National Institutes of Health (NIH R01 CA226899).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
Appears in Collections:Journal/Magazine Article
Files in This Item:
File Description SizeFormat 
1-s2.0-S2452109425001708-main.pdf1.87 MBAdobe PDFView/Open
Open Access Information
Status open access
File Version Version of Record
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.