Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/111678
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Health Technology and Informatics | en_US |
| dc.contributor | Department of Biomedical Engineering | en_US |
| dc.contributor | Mainland Development Office | en_US |
| dc.creator | Nicol, AJ | en_US |
| dc.creator | Lam, SK | en_US |
| dc.creator | Ching, JCF | en_US |
| dc.creator | Tam, VCW | en_US |
| dc.creator | Teng, X | en_US |
| dc.creator | Zhang, J | en_US |
| dc.creator | Lee, FKH | en_US |
| dc.creator | Wong, KCW | en_US |
| dc.creator | Cai, J | en_US |
| dc.creator | Lee, SWY | en_US |
| dc.date.accessioned | 2025-03-13T02:21:21Z | - |
| dc.date.available | 2025-03-13T02:21:21Z | - |
| dc.identifier.issn | 0033-8362 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/111678 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Springer Milano | en_US |
| dc.rights | © The Author(s) 2024 | en_US |
| dc.rights | This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. | en_US |
| dc.rights | The following publication Nicol, A.J., Lam, SK., Ching, J.C.F. et al. A multi-center, multi-organ, multi-omic prediction model for treatment-induced severe oral mucositis in nasopharyngeal carcinoma. Radiol med 130, 161–178 (2025) is available at https://dx.doi.org/10.1007/s11547-024-01901-z. | en_US |
| dc.subject | Dosiomics | en_US |
| dc.subject | Nasopharyngeal carcinoma | en_US |
| dc.subject | Oral mucositis | en_US |
| dc.subject | Radiomics | en_US |
| dc.subject | Toxicity | en_US |
| dc.title | A multi-center, multi-organ, multi-omic prediction model for treatment-induced severe oral mucositis in nasopharyngeal carcinoma | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 161 | en_US |
| dc.identifier.epage | 178 | en_US |
| dc.identifier.volume | 130 | en_US |
| dc.identifier.doi | 10.1007/s11547-024-01901-z | en_US |
| dcterms.abstract | Purpose: Oral mucositis (OM) is one of the most prevalent and crippling treatment-related toxicities experienced by nasopharyngeal carcinoma (NPC) patients receiving radiotherapy (RT), posing a tremendous adverse impact on quality of life. This multi-center study aimed to develop and externally validate a multi-omic prediction model for severe OM. | en_US |
| dcterms.abstract | Methods: Four hundred and sixty-four histologically confirmed NPC patients were retrospectively recruited from two public hospitals in Hong Kong. Model development was conducted on one institution (n = 363), and the other was reserved for external validation (n = 101). Severe OM was defined as the occurrence of CTCAE grade 3 or higher OM during RT. Two predictive models were constructed: 1) conventional clinical and DVH features and 2) a multi-omic approach including clinical, radiomic and dosiomic features. | en_US |
| dcterms.abstract | Results: The multi-omic model, consisting of chemotherapy status and radiomic and dosiomic features, outperformed the conventional model in internal and external validation, achieving AUC scores of 0.67 [95% CI: (0.61, 0.73)] and 0.65 [95% CI: (0.53, 0.77)], respectively, compared to the conventional model with 0.63 [95% CI: (0.56, 0.69)] and 0.56 [95% CI: (0.44, 0.67)], respectively. In multivariate analysis, only the multi-omic model signature was significantly correlated with severe OM in external validation (p = 0.017), demonstrating the independent predictive value of the multi-omic approach. | en_US |
| dcterms.abstract | Conclusion: A multi-omic model with combined clinical, radiomic and dosiomic features achieved superior pre-treatment prediction of severe OM. Further exploration is warranted to facilitate improved clinical decision-making and enable more effective and personalized care for the prevention and management of OM in NPC patients. | en_US |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | La Radiologia Medica, Feb. 2025, v. 130, p. 161-178 | en_US |
| dcterms.isPartOf | La Radiologia Medica | en_US |
| dcterms.issued | 2025-02 | - |
| dc.identifier.scopus | 2-s2.0-85209738598 | - |
| dc.identifier.eissn | 1826-6983 | en_US |
| dc.description.validate | 202503 bchy | en_US |
| dc.description.oa | Version of Record | en_US |
| dc.identifier.FolderNumber | OA_TA | - |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | Hong Kong Polytechnic University: Project of Strategic Importance and Projects of RISA | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.description.TA | Springer Nature (2024) | en_US |
| dc.description.oaCategory | TA | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| s11547-024-01901-z.pdf | 1.89 MB | Adobe PDF | View/Open |
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