A multi-center, multi-organ, multi-omic prediction model for treatment-induced severe oral mucositis in nasopharyngeal carcinoma

被引:0
|
作者
Nicol, Alexander James [1 ]
Lam, Sai-Kit [2 ]
Ching, Jerry Chi Fung [1 ]
Tam, Victor Chi Wing [1 ]
Teng, Xinzhi [1 ]
Zhang, Jiang [1 ]
Lee, Francis Kar Ho [3 ]
Wong, Kenneth C. W. [4 ]
Cai, Jing [1 ,5 ]
Lee, Shara Wee Yee [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Hlth Technol & Informat, Hung Hom, Room Y910,9-F,Block Y,Lee Shau Kee Bldg, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Dept Biomed Engn, Hung Hom, Hong Kong, Peoples R China
[3] Queen Elizabeth Hosp, Dept Clin Oncol, Yau Ma Tei, Hong Kong, Peoples R China
[4] Prince Wales Hosp, Dept Clin Oncol, Sha Tin, Hong Kong, Peoples R China
[5] Hong Kong Polytech Univ, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
来源
RADIOLOGIA MEDICA | 2025年 / 130卷 / 02期
关键词
Radiomics; Dosiomics; Oral mucositis; Toxicity; Nasopharyngeal carcinoma; SPATIAL DOSE METRICS; NECK-CANCER PATIENTS; NTCP MODELS; HEAD; RADIOTHERAPY; CHEMOTHERAPY; RISK; THERAPY; DAHANCA; EORTC;
D O I
10.1007/s11547-024-01901-z
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
PurposeOral 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.MethodsFour 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.ResultsThe 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.ConclusionA 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.
引用
收藏
页码:161 / 178
页数:18
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