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      Radiomic profiling for insular diffuse glioma stratification with distinct biologic pathway activities

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          Abstract

          Current literature emphasizes surgical complexities and customized resection for managing insular gliomas; however, radiogenomic investigations into prognostic radiomic traits remain limited. We aimed to develop and validate a radiomic model using multiparametric magnetic resonance imaging (MRI) for prognostic prediction and to reveal the underlying biological mechanisms. Radiomic features from preoperative MRI were utilized to develop and validate a radiomic risk signature (RRS) for insular gliomas, validated through paired MRI and RNA‐seq data ( N = 39), to identify core pathways underlying the RRS and individual prognostic radiomic features. An 18‐feature‐based RRS was established for overall survival (OS) prediction. Gene set enrichment analysis (GSEA) and weighted gene coexpression network analysis (WGCNA) were used to identify intersectional pathways. In total, 364 patients with insular gliomas (training set, N = 295; validation set, N = 69) were enrolled. RRS was significantly associated with insular glioma OS (log‐rank p = 0.00058; HR = 3.595, 95% CI:1.636–7.898) in the validation set. The radiomic‐pathological‐clinical model (R‐P‐CM) displayed enhanced reliability and accuracy in prognostic prediction. The radiogenomic analysis revealed 322 intersectional pathways through GSEA and WGCNA fusion; 13 prognostic radiomic features were significantly correlated with these intersectional pathways. The RRS demonstrated independent predictive value for insular glioma prognosis compared with established clinical and pathological profiles. The biological basis for prognostic radiomic indicators includes immune, proliferative, migratory, metabolic, and cellular biological function‐related pathways.

          Abstract

          We believe that our study makes a significant contribution to the literature because it introduced a prognostic radiomic risk signature (RRS), which allowed the noninvasive stratification of insular glioma patients and complemented the molecular diagnosis‐based glioma classification. Furthermore, it revealed the factors that influence prognostic radiomic traits, providing insights that offer strategies for targeted therapy and tailored management of insular gliomas.

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          Most cited references47

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          The 2021 WHO Classification of Tumors of the Central Nervous System: a summary

          The fifth edition of the WHO Classification of Tumors of the Central Nervous System (CNS), published in 2021, is the sixth version of the international standard for the classification of brain and spinal cord tumors. Building on the 2016 updated fourth edition and the work of the Consortium to Inform Molecular and Practical Approaches to CNS Tumor Taxonomy, the 2021 fifth edition introduces major changes that advance the role of molecular diagnostics in CNS tumor classification. At the same time, it remains wedded to other established approaches to tumor diagnosis such as histology and immunohistochemistry. In doing so, the fifth edition establishes some different approaches to both CNS tumor nomenclature and grading and it emphasizes the importance of integrated diagnoses and layered reports. New tumor types and subtypes are introduced, some based on novel diagnostic technologies such as DNA methylome profiling. The present review summarizes the major general changes in the 2021 fifth edition classification and the specific changes in each taxonomic category. It is hoped that this summary provides an overview to facilitate more in-depth exploration of the entire fifth edition of the WHO Classification of Tumors of the Central Nervous System.
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            The Image Biomarker Standardization Initiative: Standardized Quantitative Radiomics for High-Throughput Image-based Phenotyping

            Background Radiomic features may quantify characteristics present in medical imaging. However, the lack of standardized definitions and validated reference values have hampered clinical use. Purpose To standardize a set of 174 radiomic features. Materials and Methods Radiomic features were assessed in three phases. In phase I, 487 features were derived from the basic set of 174 features. Twenty-five research teams with unique radiomics software implementations computed feature values directly from a digital phantom, without any additional image processing. In phase II, 15 teams computed values for 1347 derived features using a CT image of a patient with lung cancer and predefined image processing configurations. In both phases, consensus among the teams on the validity of tentative reference values was measured through the frequency of the modal value and classified as follows: less than three matches, weak; three to five matches, moderate; six to nine matches, strong; 10 or more matches, very strong. In the final phase (phase III), a public data set of multimodality images (CT, fluorine 18 fluorodeoxyglucose PET, and T1-weighted MRI) from 51 patients with soft-tissue sarcoma was used to prospectively assess reproducibility of standardized features. Results Consensus on reference values was initially weak for 232 of 302 features (76.8%) at phase I and 703 of 1075 features (65.4%) at phase II. At the final iteration, weak consensus remained for only two of 487 features (0.4%) at phase I and 19 of 1347 features (1.4%) at phase II. Strong or better consensus was achieved for 463 of 487 features (95.1%) at phase I and 1220 of 1347 features (90.6%) at phase II. Overall, 169 of 174 features were standardized in the first two phases. In the final validation phase (phase III), most of the 169 standardized features could be excellently reproduced (166 with CT; 164 with PET; and 164 with MRI). Conclusion A set of 169 radiomics features was standardized, which enabled verification and calibration of different radiomics software. © RSNA, 2020 Online supplemental material is available for this article. See also the editorial by Kuhl and Truhn in this issue.
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              Immunotherapy for glioma: current management and future application

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                Author and article information

                Contributors
                xzliu06@126.com
                fcczhangzy1@zzu.edu.cn
                fccyanj@zzu.edu.cn
                Journal
                Cancer Sci
                Cancer Sci
                10.1111/(ISSN)1349-7006
                CAS
                Cancer Science
                John Wiley and Sons Inc. (Hoboken )
                1347-9032
                1349-7006
                26 January 2024
                April 2024
                : 115
                : 4 ( doiID: 10.1111/cas.v115.4 )
                : 1261-1272
                Affiliations
                [ 1 ] Department of Neurosurgery The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan China
                [ 2 ] Department of MRI The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan China
                Author notes
                [*] [* ] Correspondence

                Xianzhi Liu, Department of Neurosurgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province 450052, China.

                Email: xzliu06@ 123456126.com

                Zhenyu Zhang, Department of Neurosurgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province 450052, China.

                Email: fcczhangzy1@ 123456zzu.edu.cn

                Jing Yan, Department of MRI, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province 450052, China.

                Email: fccyanj@ 123456zzu.edu.cn

                Author information
                https://orcid.org/0000-0001-6245-7434
                Article
                CAS16089 CAS-OA-2082-2023.R1
                10.1111/cas.16089
                11007007
                38279197
                835b5a2e-3e6b-49db-8834-9c7956c07fce
                © 2024 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 31 December 2023
                : 04 September 2023
                : 05 January 2024
                Page count
                Figures: 6, Tables: 2, Pages: 12, Words: 6792
                Funding
                Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
                Award ID: 82102149
                Award ID: 82173090
                Award ID: 82273493
                Funded by: Health Commission of Henan Province , doi 10.13039/100018925;
                Award ID: YXKC2022061
                Award ID: BGJ202002062
                Funded by: Natural Science Foundation of Henan Province , doi 10.13039/501100006407;
                Award ID: 232300421057
                Funded by: Henan Provincial Science and Technology Research Project , doi 10.13039/501100017700;
                Award ID: 192102310390
                Award ID: 202102310136
                Award ID: 202102310454
                Award ID: 212102310113
                Categories
                Original Article
                ORIGINAL ARTICLES
                Clinical Research
                Custom metadata
                2.0
                April 2024
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.4.0 mode:remove_FC converted:11.04.2024

                Oncology & Radiotherapy
                biological pathway,insular glioma,machine learning,prognosis,radiomic features

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