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      Molecular diagnostic tools for the World Health Organization (WHO) 2021 classification of gliomas, glioneuronal and neuronal tumors; an EANO guideline

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          Abstract

          In the 5th edition of the WHO CNS tumor classification (CNS5, 2021), multiple molecular characteristics became essential diagnostic criteria for many additional CNS tumor types. For those tumors, an integrated, “histomolecular” diagnosis is required. A variety of approaches exists for determining the status of the underlying molecular markers. The present guideline focuses on the methods that can be used for assessment of the currently most informative diagnostic and prognostic molecular markers for the diagnosis of gliomas, glioneuronal and neuronal tumors. The main characteristics of the molecular methods are systematically discussed, followed by recommendations and information on available evidence levels for diagnostic measures. The recommendations cover DNA and RNA next-generation-sequencing, methylome profiling, and select assays for single/limited target analyses, including immunohistochemistry. Additionally, because of its importance as a predictive marker in IDH-wildtype glioblastomas, tools for the analysis of MGMT promoter methylation status are covered. A structured overview of the different assays with their characteristics, especially their advantages and limitations, is provided, and requirements for input material and reporting of results are clarified. General aspects of molecular diagnostic testing regarding clinical relevance, accessibility, cost, implementation, regulatory, and ethical aspects are discussed as well. Finally, we provide an outlook on new developments in the landscape of molecular testing technologies in neuro-oncology.

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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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            MGMT gene silencing and benefit from temozolomide in glioblastoma.

            Epigenetic silencing of the MGMT (O6-methylguanine-DNA methyltransferase) DNA-repair gene by promoter methylation compromises DNA repair and has been associated with longer survival in patients with glioblastoma who receive alkylating agents. We tested the relationship between MGMT silencing in the tumor and the survival of patients who were enrolled in a randomized trial comparing radiotherapy alone with radiotherapy combined with concomitant and adjuvant treatment with temozolomide. The methylation status of the MGMT promoter was determined by methylation-specific polymerase-chain-reaction analysis. The MGMT promoter was methylated in 45 percent of 206 assessable cases. Irrespective of treatment, MGMT promoter methylation was an independent favorable prognostic factor (P<0.001 by the log-rank test; hazard ratio, 0.45; 95 percent confidence interval, 0.32 to 0.61). Among patients whose tumor contained a methylated MGMT promoter, a survival benefit was observed in patients treated with temozolomide and radiotherapy; their median survival was 21.7 months (95 percent confidence interval, 17.4 to 30.4), as compared with 15.3 months (95 percent confidence interval, 13.0 to 20.9) among those who were assigned to only radiotherapy (P=0.007 by the log-rank test). In the absence of methylation of the MGMT promoter, there was a smaller and statistically insignificant difference in survival between the treatment groups. Patients with glioblastoma containing a methylated MGMT promoter benefited from temozolomide, whereas those who did not have a methylated MGMT promoter did not have such a benefit. Copyright 2005 Massachusetts Medical Society.
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              DNA sequencing with chain-terminating inhibitors

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                Author and article information

                Contributors
                Journal
                Neuro Oncol
                Neuro Oncol
                neuonc
                Neuro-Oncology
                Oxford University Press (US )
                1522-8517
                1523-5866
                October 2023
                02 June 2023
                02 June 2023
                : 25
                : 10
                : 1731-1749
                Affiliations
                Department of Neuropathology, University Hospital Heidelberg , Heidelberg, Germany
                CCU Neuropathology, German Concortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ) , Heidelberg, Germany
                Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology and Division of Neuropathology, The National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Foundation Trust , London, UK
                Pathology Unit, Department of Medical Sciences, University of Turin , Turin, Italy
                Department of Neuropathology, Charité, Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin , Berlin, Germany
                German Cancer Consortium (DKTK), Partner Site Berlin, German Cancer Research Center (DKFZ) , Heidelberg, Germany
                Department of Neurology, Brain Tumor Center at Erasmus MC Cancer Center , 3015 GD Rotterdam, The Netherlands
                Aix-Marseille University, APHM, CNRS, INP, Institute Neurophysiopathol, CHU Timone, Service d’Anatomie Pathologique et de Neuropathologie , Marseille, France
                Department of Radiological, Oncological and Anatomo-Pathological Sciences, University Sapienza of Rome , Rome, Italy
                Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna , Austria
                Neuroscience Research Center and Neurosurgery, Lausanne University Hospital and University of Lausanne , Switzerland
                Department of Clinical Medicine and Biotech Research and Innovation Center (BRIC), University of Copenhagen , Denmark
                Department of Pathology, The Bartholin Institute, Rigshospitalet, Copenhagen University Hospital , Copenhagen, Denmark
                Brain Tumour Research Centre, University of Bristol , UK
                Division of Oncology, Department of Medicine I, Medical University of Vienna , Austria
                Princess Máxima Center for Pediatric Oncology , Utrecht, The Netherlands
                The Brain Tumor Center at Erasmus MC Cancer Institute , Rotterdam, The Netherlands
                Department of Neurology and Neurooncology Program, National Center for Tumor Diseases, Heidelberg University Hospital
                Clinical Cooperation Unit Neurooncology, German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ) , Heidelberg, Germany
                Institute of Neuropathology, Heinrich Heine University, Medical Faculty, and University Hospital Düsseldorf, and German Cancer Consortium (DKTK), Partner Site Essen/Düsseldorf , Düsseldorf, Germany
                Department of Pathology, Amsterdam University Medical Centers , Amsterdam, The Netherlands
                Princess Máxima Center for Pediatric Oncology , Utrecht, The Netherlands (P.W.)
                Author notes
                Corresponding Authors: Felix Sahm, MD, Department of Neuropathology, University Hospital Heidelberg, and CCU Neuropathology, German Concortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany ( felix.sahm@ 123456med.uni-heidelberg.de )
                Pieter Wesseling, MD, PhD, Department of Pathology, Amsterdam University Medical Centers, Amsterdam, The Netherlands, and Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands ( p.wesseling@ 123456amsterdamumc.nl ).

                Deceased; see paragraph ’Dedication’ at the end of the article

                Author information
                https://orcid.org/0000-0001-5441-1962
                https://orcid.org/0000-0002-9821-0342
                https://orcid.org/0000-0001-9887-7668
                https://orcid.org/0000-0003-1945-497X
                https://orcid.org/0000-0002-0668-9529
                https://orcid.org/0000-0002-3604-887X
                https://orcid.org/0000-0003-1016-0545
                https://orcid.org/0000-0003-0855-6495
                https://orcid.org/0000-0002-6352-0826
                https://orcid.org/0000-0001-8161-1302
                https://orcid.org/0000-0003-3541-2315
                https://orcid.org/0000-0002-1699-8210
                https://orcid.org/0000-0001-5710-5127
                https://orcid.org/0000-0002-6171-634X
                https://orcid.org/0000-0001-5453-5201
                Article
                noad100
                10.1093/neuonc/noad100
                10547522
                37279174
                00a60665-a647-4a2c-adb1-d73b038632a2
                © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 19 July 2023
                Page count
                Pages: 19
                Categories
                Guidelines
                Editor's Choice
                AcademicSubjects/MED00300
                AcademicSubjects/MED00310

                Oncology & Radiotherapy
                glioma,glioneuronal tumors,molecular classification,molecular diagnostics,neuronal tumors,who classification

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