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Article: Next-generation AI framework for comprehensive oral leukoplakia evaluation and management.

TitleNext-generation AI framework for comprehensive oral leukoplakia evaluation and management.
Authors
Issue Date10-Aug-2025
PublisherNature Research
Citation
npj Digital Medicine, 2025, v. 8, n. 1 How to Cite?
AbstractOral potentially malignant disorder poses a significant risk of malignant transformation, particularly in cases with epithelial dysplasia (OED). Current OED assessment methods are invasive and lack reliable decision-support tools for cancer risk evaluation and follow-up optimization. This study developed and validated OMMT-PredNet, a fully automated multimodal deep learning framework requiring no manual ROI annotation, for non-invasive OED identification and time-dependent cancer risk prediction. Utilizing data from 649 histopathologically confirmed leukoplakia cases across multiple institutions (2003-2024), including 598 cases in the primary cohort and 51 in the external validation set, the model integrated paired high-resolution clinical images and medical records. OMMT-PredNet achieved an AUC of 0.9592 (95% CI: 0.9491-0.9693) for cancer risk prediction and 0.9219 (95% CI: 0.9088-0.9349) for OED identification, with high specificity (MT: 0.9490; OED: 0.9182) and precision (MT: 0.9442; OED: 0.9303). Calibration and decision curve analyses confirmed clinical applicability, while external validation demonstrated robustness. This multidimensional model effectively predicts OED and cancer risk, highlighting its global applicability in enhancing oral cancer screening and improving patient outcomes.
Persistent Identifierhttp://hdl.handle.net/10722/366494
ISSN
2023 Impact Factor: 12.4
2023 SCImago Journal Rankings: 4.273

 

DC FieldValueLanguage
dc.contributor.authorLi, JingWen-
dc.contributor.authorZhou, YaFang-
dc.contributor.authorZhang, MengJing-
dc.contributor.authorAdeoye, John-
dc.contributor.authorPu, Jane JingYa-
dc.contributor.authorZhou, MiMi-
dc.contributor.authorLiu, ChuanXia-
dc.contributor.authorFan, LiJie-
dc.contributor.authorMcGrath, Colman-
dc.contributor.authorZhang, Dian-
dc.contributor.authorZheng, LiWu-
dc.date.accessioned2025-11-25T04:19:43Z-
dc.date.available2025-11-25T04:19:43Z-
dc.date.issued2025-08-10-
dc.identifier.citationnpj Digital Medicine, 2025, v. 8, n. 1-
dc.identifier.issn2398-6352-
dc.identifier.urihttp://hdl.handle.net/10722/366494-
dc.description.abstractOral potentially malignant disorder poses a significant risk of malignant transformation, particularly in cases with epithelial dysplasia (OED). Current OED assessment methods are invasive and lack reliable decision-support tools for cancer risk evaluation and follow-up optimization. This study developed and validated OMMT-PredNet, a fully automated multimodal deep learning framework requiring no manual ROI annotation, for non-invasive OED identification and time-dependent cancer risk prediction. Utilizing data from 649 histopathologically confirmed leukoplakia cases across multiple institutions (2003-2024), including 598 cases in the primary cohort and 51 in the external validation set, the model integrated paired high-resolution clinical images and medical records. OMMT-PredNet achieved an AUC of 0.9592 (95% CI: 0.9491-0.9693) for cancer risk prediction and 0.9219 (95% CI: 0.9088-0.9349) for OED identification, with high specificity (MT: 0.9490; OED: 0.9182) and precision (MT: 0.9442; OED: 0.9303). Calibration and decision curve analyses confirmed clinical applicability, while external validation demonstrated robustness. This multidimensional model effectively predicts OED and cancer risk, highlighting its global applicability in enhancing oral cancer screening and improving patient outcomes.-
dc.languageeng-
dc.publisherNature Research-
dc.relation.ispartofnpj Digital Medicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleNext-generation AI framework for comprehensive oral leukoplakia evaluation and management.-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41746-025-01885-8-
dc.identifier.pmid40784991-
dc.identifier.volume8-
dc.identifier.issue1-
dc.identifier.eissn2398-6352-
dc.identifier.issnl2398-6352-

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