Development and validation of a CT-based radiomics signature for identifying high-risk neuroblastomas under the revised Children's Oncology Group classification system.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
05 2023
Historique:
revised: 09 02 2023
received: 07 12 2022
accepted: 13 02 2023
pubmed: 8 3 2023
medline: 25 3 2023
entrez: 7 3 2023
Statut: ppublish

Résumé

To develop and validate a radiomics signature based on computed tomography (CT) for identifying high-risk neuroblastomas. This retrospective study included 339 patients with neuroblastomas, who were classified into high-risk and non-high-risk groups according to the revised Children's Oncology Group classification system. These patients were then randomly divided into a training set (n = 237) and a testing set (n = 102). Pretherapy CT images of the arterial phase were segmented by two radiologists. Pyradiomics package and FeAture Explorer software were used to extract and process radiomics features. Radiomics models based on linear discriminant analysis (LDA), logistic regression (LR), and support vector machine (SVM) were constructed, and the area under the curve (AUC), 95% confidence interval (CI), and accuracy were calculated. The optimal LDA, LR, and SVM models had 11, 12, and 14 radiomics features, respectively. The AUC of the LDA model in the training and testing sets were 0.877 (95% CI: 0.833-0.921) and 0.867 (95% CI: 0.797-0.937), with an accuracy of 0.823 and 0.804, respectively. The AUC of the LR model in the training and testing sets were 0.881 (95% CI: 0.839-0.924) and 0.855 (95% CI: 0.781-0.930), with an accuracy of 0.823 and 0.804, respectively. The AUC of the SVM model in the training and testing sets were 0.879 (95% CI: 0.836-0.923) and 0.862 (95% CI: 0.791-0.934), with an accuracy of 0.827 and 0.804, respectively. CT-based radiomics is able to identify high-risk neuroblastomas and may provide additional image biomarkers for the identification of high-risk neuroblastomas.

Sections du résumé

BACKGROUND
To develop and validate a radiomics signature based on computed tomography (CT) for identifying high-risk neuroblastomas.
PROCEDURE
This retrospective study included 339 patients with neuroblastomas, who were classified into high-risk and non-high-risk groups according to the revised Children's Oncology Group classification system. These patients were then randomly divided into a training set (n = 237) and a testing set (n = 102). Pretherapy CT images of the arterial phase were segmented by two radiologists. Pyradiomics package and FeAture Explorer software were used to extract and process radiomics features. Radiomics models based on linear discriminant analysis (LDA), logistic regression (LR), and support vector machine (SVM) were constructed, and the area under the curve (AUC), 95% confidence interval (CI), and accuracy were calculated.
RESULTS
The optimal LDA, LR, and SVM models had 11, 12, and 14 radiomics features, respectively. The AUC of the LDA model in the training and testing sets were 0.877 (95% CI: 0.833-0.921) and 0.867 (95% CI: 0.797-0.937), with an accuracy of 0.823 and 0.804, respectively. The AUC of the LR model in the training and testing sets were 0.881 (95% CI: 0.839-0.924) and 0.855 (95% CI: 0.781-0.930), with an accuracy of 0.823 and 0.804, respectively. The AUC of the SVM model in the training and testing sets were 0.879 (95% CI: 0.836-0.923) and 0.862 (95% CI: 0.791-0.934), with an accuracy of 0.827 and 0.804, respectively.
CONCLUSIONS
CT-based radiomics is able to identify high-risk neuroblastomas and may provide additional image biomarkers for the identification of high-risk neuroblastomas.

Identifiants

pubmed: 36881504
doi: 10.1002/pbc.30280
doi:

Substances chimiques

Biomarkers 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e30280

Informations de copyright

© 2023 Wiley Periodicals LLC.

Références

Lundberg KI, Treis D, Johnsen JI. Neuroblastoma heterogeneity, plasticity, and emerging therapies. Curr Oncol Rep. 2022;24:1053-1062.
Shawraba F, Hammoud H, Mrad Y, et al. Biomarkers in neuroblastoma: an insight into their potential diagnostic and prognostic utilities. Curr Treat Options Oncol. 2021;22:102.
Ponzoni M, Bachetti T, Corrias MV, et al. Recent advances in the developmental origin of neuroblastoma: an overview. J Exp Clin Cancer Res. 2022;41:92.
Irwin MS, Naranjo A, Zhang FF, et al. Revised neuroblastoma risk classification system: a report from the Children's Oncology Group. J Clin Oncol. 2021;39:3229-3241.
Schmelz K, Toedling J, Huska M, et al. Spatial and temporal intratumour heterogeneity has potential consequences for single biopsy-based neuroblastoma treatment decisions. Nat Commun. 2021;12:6804.
Lambin P, Rios-Velazquez E, Leijenaar R, et al. Radiomics: extracting more information from medical images using advanced feature analysis. Eur J Cancer. 2012;48:441-446.
Wang X, Pennello G, deSouza NM, et al. Multiparametric data-driven imaging markers: guidelines for development, application and reporting of model outputs in radiomics. Acad Radiol. 2023;30:215-229.
Rogers W, Thulasi Seetha S, Refaee TAG, et al. Radiomics: from qualitative to quantitative imaging. Br J Radiol. 2020;93(1108):20190948.
Di Giannatale A, Di Paolo PL, Curione D, et al. Radiogenomics prediction for MYCN amplification in neuroblastoma: a hypothesis generating study. Pediatr Blood Cancer. 2021;68:e29110.
Wang H, Chen X, Liu H, et al. Computed tomography-based radiomics for differential of retroperitoneal neuroblastoma and ganglioneuroblastoma in children. Nan Fang Yi Ke Da Xue Xue Bao. 2021;41:1569-1576.
Liu G, Poon M, Zapala MA, et al. Incorporating radiomics into machine learning models to predict outcomes of neuroblastoma. J Digit Imaging. 2022;35:605-612.
Wang H, Qin J, Chen X, et al. Contrast-enhanced computed tomography radiomics in predicting primary site response to neoadjuvant chemotherapy in high-risk neuroblastoma. Abdom Radiol (NY). 2023;48(3):976-986. doi:10.1007/s00261-022-03774-0
Yushkevich PA, Piven J, Hazlett HC, et al. User-guided 3D active contour segmentation of anatomical structures: significantly improved efficiency and reliability. Neuroimage. 2006;31:1116-1128.
van Griethuysen JJM, Fedorov A, Parmar C, et al. Computational radiomics system to decode the radiographic phenotype. Cancer Res. 2017;77:e104-e107.
Zwanenburg A, Vallières M, Abdalah MA, et al. The image biomarker standardization initiative: standardized quantitative radiomics for high-throughput image-based phenotyping. Radiology. 2020;295:328-338.
Chawla NV, Bowyer KW, Hall LO, et al. SMOTE: synthetic minority over-sampling technique. J Artif Intell Res. 2002;16:321-357. doi:10.48550/arXiv.1106.1813
Wu H, Wu C, Zheng H, et al. Radiogenomics of neuroblastoma in pediatric patients: CT-based radiomics signature in predicting MYCN amplification. Eur Radiol. 2021;31:3080-3089.
Karami G, Giuseppe Orlando M, Delli Pizzi A, et al. Predicting overall survival time in glioblastoma patients using gradient boosting machines algorithm and recursive feature elimination technique. Cancers (Basel). 2021;13:4976.
Chen Y, Yang Y. The one standard error rule for model selection: does it work? Stats. 2021;4:868-892.
Song Y, Zhang J, Zhang YD, et al. FeAture Explorer (FAE): a tool for developing and comparing radiomics models. PLoS One. 2020;15:e0237587.
Tolbert VP, Matthay KK. Neuroblastoma: clinical and biological approach to risk stratification and treatment. Cell Tissue Res. 2018;372:195-209.
Swift CC, Eklund MJ, Kraveka JM, et al. Updates in diagnosis, management, and treatment of neuroblastoma. Radiographics. 2018;38:566-580.
Bar-Sever Z, Biassoni L, Shulkin B, et al. Guidelines on nuclear medicine imaging in neuroblastoma. Eur J Nucl Med Mol Imaging. 2018;45:2009-2024.
Schriegel F, Taschner-Mandl S, Bernkopf M, et al. Comparison of three different methods to detect bone marrow involvement in patients with neuroblastoma. J Cancer Res Clin Oncol. 2022;148:2581-2588.
Qian L, Yang S, Zhang S, et al. Prediction of MYCN amplification, 1p and 11q aberrations in pediatric neuroblastoma via pre-therapy 18F-FDG PET/CT radiomics. Front Med (Lausanne). 2022;9:840777.
Feng L, Lu X, Yang X, et al. An 18F-FDG PET/CT radiomics nomogram for differentiation of high-risk and non-high-risk patients of the International Neuroblastoma Risk Group Staging System. Eur J Radiol. 2022;154:110444.
Callahan MJ, MacDougall RD, Bixby SD, et al. Ionizing radiation from computed tomography versus anesthesia for magnetic resonance imaging in infants and children: patient safety considerations. Pediatr Radiol. 2018;48:21-30.
Burnand K, Barone G, McHugh K, et al. Preoperative computed tomography scanning for abdominal neuroblastomas is superior to magnetic resonance imaging for safe surgical planning. Pediatr Blood Cancer. 2019;66:e27955.
Chen X, Wang H, Huang K, et al. CT-based radiomics signature with machine learning predicts MYCN amplification in pediatric abdominal neuroblastoma. Front Oncol. 2021;11:687884.
Ahn H, Song GJ, Jang SH, et al. Relationship of FDG PET/CT Textural Features with the Tumor Microenvironment and Recurrence Risks in Patients with Advanced Gastric Cancers. Cancers (Basel). 2022;14:3936.
Lee HK, Kim CH, Bhattacharjee S, et al. A paradigm shift in nuclear chromatin interpretation: from qualitative intuitive recognition to quantitative texture analysis of breast cancer cell nuclei. Cytometry A. 2021;99:698-706.
Fan X, Xue N, Han Z, et al. Wavelet transform artificial intelligence algorithm-based data mining technology for norovirus monitoring and early warning. J Healthc Eng. 2021;2021:6128260.

Auteurs

Haoru Wang (H)

Department of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Mingye Xie (M)

Department of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Xin Chen (X)

Department of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Jin Zhu (J)

Department of Pathology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Hao Ding (H)

Department of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Li Zhang (L)

Department of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Zhengxia Pan (Z)

Department of Cardiothoracic Surgery, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Ling He (L)

Department of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH