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
相关论文
共 50 条
  • [21] Defibrotide (DF) for the treatment of severe veno-occlusive disease (sVOD) and multi-organ failure (MOF) post SCT: Final results of a multi-center, randomized, dose-finding trial.
    Richardson, Paul
    Soiffer, R. J.
    Antin, J. H.
    Jin, Z.
    Kurtzberg, J.
    Martin, P. L.
    Steinbach, G.
    Murray, K. F.
    Vogelsang, G. B.
    Chen, A.
    Krishnan, A.
    Kernan, N. A.
    Avigan, D.
    Spitzer, T. R.
    Warren, D.
    Revta, C.
    Wei, L. J.
    Iacobelli, M.
    McDonald, G. B.
    Guinan, E. C.
    BLOOD, 2006, 108 (11) : 17A - 18A
  • [22] Improvement in the prediction power of an astrocyte genome-scale metabolic model using multi-omic data
    Angarita-Rodriguez, Andrea
    Mendoza-Mejia, Nicolas
    Gonzalez, Janneth
    Papin, Jason
    Aristizabal, Andres Felipe
    Pinzon, Andres
    FRONTIERS IN SYSTEMS BIOLOGY, 2025, 4
  • [23] Multi-omic analyses reveal aberrant DNA methylation patterns and the associated biomarkers of nasopharyngeal carcinoma and its cancer stem cells
    Jiang, Yike
    Yang, Hongtian
    Ye, Zilu
    Huang, Yunchuanxiang
    Li, Ping
    Jiang, Ziyi
    Han, Sanyang
    Ma, Lan
    SCIENTIFIC REPORTS, 2025, 15 (01):
  • [24] An integrative model of multi-organ drug-induced toxicity prediction using gene-expression data
    Jinwoo Kim
    Miyoung Shin
    BMC Bioinformatics, 15
  • [25] An integrative model of multi-organ drug-induced toxicity prediction using gene-expression data
    Kim, Jinwoo
    Shin, Miyoung
    BMC BIOINFORMATICS, 2014, 15
  • [26] A multi-label learning model for predicting drug-induced pathology in multi-organ based on toxicogenomics data
    Su, Ran
    Yang, Haitang
    Wei, Leyi
    Chen, Siqi
    Zou, Quan
    PLOS COMPUTATIONAL BIOLOGY, 2022, 18 (09)
  • [27] A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation (vol 19, 255, 2023)
    Monte, Andrew A.
    Vest, Alexis
    Reisz, Julie A.
    Berninzoni, Danielle
    Hart, Claire
    Dylla, Layne
    D'Alessandro, Angelo
    Heard, Kennon J.
    Wood, Cheyret
    Pattee, Jack
    JOURNAL OF MEDICAL TOXICOLOGY, 2023, 19 (04) : 416 - 416
  • [28] multi-modality prediction of radiation induced hypothyroidism for nasopharyngeal carcinoma patients
    Wu, Jiaming
    Zhang, Jiang
    Teng, Xinzhi
    Zhang, Xinyu
    Sun, Jiachen
    Cheung, Ka Man
    Lui, C. F. Jeffrey
    Yip, W. Y. Celia
    Lee, K. H. Francis
    Chow, C. H. James
    Cai, Jing
    RADIOTHERAPY AND ONCOLOGY, 2024, 194 : S5057 - S5058
  • [29] INTEGRATED MULTI-OMIC AND CLINICOPATHOLOGICAL ANALYSIS OF VULVAR SQUAMOUS CELL CARCINOMA: IDENTIFICATION OF PREDICTIVE BIOMARKERS FOR PERSONALIZED TREATMENT
    Zwimpfer, Tibor A.
    Lombardo, Flavio
    Rimmer, Natalie
    Gotze, Sandra
    Singer, Franziska
    Bertolini, Anne
    Montavon, Celine
    Kurzeder, Christian
    Jacob, Francis
    Heinzelmann-Schwarz, Viola
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2023, 33 : A364 - A364
  • [30] Multi-organ procurement and successful multi-center allocation using rapid en bloc technique from a controlled non-heart-beating donor
    Moon, JI
    Nishida, S
    Butt, F
    Schwartz, CB
    Ganz, S
    Levi, DM
    Burke, GW
    Tzakis, AG
    TRANSPLANTATION, 2004, 77 (09) : 1476 - 1477