Clinical implications of the 2021 edition of the WHO classification of central nervous system tumours
Abstract
A new edition of the WHO classification of tumours of the CNS was published in 2021. Although the previous edition of this classification was published just 5 years earlier, in 2016, rapid advances in our understanding of the molecular underpinnings of CNS tumours, including the diversity of clinically relevant molecular types and subtypes, necessitated a new classification system. Compared with the 2016 scheme, the new classification incorporates even more molecular alterations into the diagnosis of many tumours and reorganizes gliomas into adult-type diffuse gliomas, paediatric-type diffuse low-grade and high-grade gliomas, circumscribed astrocytic gliomas, and ependymal tumours. A number of new entities are incorporated into the 2021 classification, especially tumours that preferentially or exclusively arise in the paediatric population. Such a substantial revision of the WHO scheme will have major implications for the diagnosis and treatment of patients with CNS tumours. In this Perspective, we summarize the main changes in the classification of diffuse and circumscribed gliomas, ependymomas, embryonal tumours and meningiomas, and discuss how each change will influence post-surgical treatment, clinical trial enrolment and cooperative studies. Although the 2021 WHO classification of CNS tumours is a major conceptual advance, its implementation on a routine clinical basis presents some challenges that will require innovative solutions.
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Glioma is the most prevalent central nervous system tumor and is classified into four grades by the World Health Organization.
“Glioma is the most prevalent central nervous system tumor and is classified into four grades, grades I, II, III, and IV, by the World Health Organization [44].”
From 5-Aminolevulinic Acid as a Theranostic Agent for Tumor Fluorescence Imaging and Photodynamic Therapy (2023) · cites this paper as [44]
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Self-citationWhat do we know about IDH1/2 mutations so far, and how do we use it?
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Ependymoma: Evaluation and Management Updates
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Ultra high-risk PFA ependymoma is characterized by loss of chromosome 6q
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Self-citationMolecular characterization of histopathological ependymoma variants
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- Authors
- Horbinski, C., Berger, T., Packer, R. J., & Wen, P. Y.
- Affiliations
- Northwestern University (US)
- Brigham and Women's Hospital (US)
- Children's National (US)
- Corresponding author
- Horbinski, Craig
- Venue
- Nature Reviews Neurology
- Published
- 2022-06-21
- Volume
- 18
- Issue
- 9
- Pages
- 515-529
- ISSN
- 1759-4758 (ISSN-L)
- 1759-4766
- OpenAlex
- W4283213286
- Cited by
- 312
- References
- 125
- Citations by year
- 2026: 59 · 2025: 83 · 2024: 86 · 2023: 71 · 2022: 12
- FWCI
- 10.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature Reviews Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (P50CA221747, K12CA090354)
- National Institute of Neurological Disorders and Stroke (R01NS118039, R01NS102669, R01NS117104)
- Topics
- Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
- Health Sciences › Medicine › Physiology › Tuberous Sclerosis Complex Research
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- diffuse glioma, ependymoma, embryonal tumors, meningioma, pediatric brain tumors, inclusion and exclusion criteria, postoperative care
- MeSH terms
- Brain Neoplasms, Child, Glioma, Humans, Meningeal Neoplasms, Meningioma, World Health Organization, Central Nervous System Neoplasms
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