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World Health Organization 2021 Classification of Central Nervous System Tumors and Implications for Therapy for
Tamar R Berger1,2, Patrick Y Wen1,2,3, Melanie Lang-Orsini4
1Division of Neuro-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Importance:
Previous histologic classifications of brain tumors have been limited by discrepancies in diagnoses reported by neuropathologists and variability in outcomes and response to therapies. Such diagnostic discrepancies have impaired clinicians' ability to select the most appropriate therapies for patients and have allowed heterogeneous populations of patients to be enrolled in clinical trials, hindering the development of more effective therapies. In adult-type diffuse gliomas, histologic classification has a particularly important effect on clinical care.
Observations:
In 2021, the World Health Organization published the fifth edition of the Classification of Tumors of the Central Nervous System. This classification incorporates advances in understanding the molecular pathogenesis of brain tumors with histopathology in order to group tumors into more biologically and molecularly defined entities. As such, tumor classification is significantly improved through better characterized natural histories. These changes have particularly important implications for gliomas. For the first time, adult- and pediatric-type gliomas are classified separately on the basis of differences in molecular pathogenesis and prognosis. Furthermore, the previous broad category of adult-type diffuse gliomas has been consolidated into 3 types: astrocytoma, isocitrate dehydrogenase (IDH) mutant; oligodendroglioma, IDH mutant and 1p/19q codeleted; and glioblastoma, IDH wild type. These major changes are driven by IDH mutation status and include the restriction of the diagnosis of glioblastoma to tumors that are IDH wild type; the reclassification of tumors previously diagnosed as IDH-mutated glioblastomas as astrocytomas IDH mutated, grade 4; and the requirement for the presence of IDH mutations to classify tumors as astrocytomas or oligodendrogliomas.
Conclusions And Relevance:
The 2021 World Health Organization central nervous system tumor classification is a major advance toward improving the diagnosis of brain tumors. It will provide clinicians with more accurate guidance on prognosis and optimal therapy for patients and ensure that more homogenous patient populations are enrolled in clinical trials, potentially facilitating the development of more effective therapies.
Insights
The 2021 World Health Organization CNS tumor classification refines brain tumor diagnosis by integrating molecular data. This improves glioma classification, impacting patient care and clinical trials.
Area of Science:
- Neuropathology
- Molecular Biology
- Oncology
Background:
- Previous brain tumor classifications faced diagnostic discrepancies and outcome variability.
- These issues hindered accurate patient therapy selection and clinical trial enrollment.
- Histologic classification significantly impacts adult-type diffuse glioma clinical care.
Approach:
- The 2021 World Health Organization Classification of Tumors of the Central Nervous System integrates histopathology with molecular pathogenesis.
- Tumors are grouped into more biologically and molecularly defined entities with better-characterized natural histories.
- Adult- and pediatric-type gliomas are now classified separately based on molecular differences and prognosis.
Key Points:
- Adult-type diffuse gliomas are consolidated into three types: astrocytoma (IDH mutant), oligodendroglioma (IDH mutant, 1p/19q codeleted), and glioblastoma (IDH wild type).
- Glioblastoma diagnosis is restricted to IDH wild-type tumors.
- IDH mutation status is critical for classifying astrocytomas and oligodendrogliomas.
Conclusions:
- The 2021 WHO CNS tumor classification represents a significant advancement in brain tumor diagnosis.
- It offers improved prognostic guidance and optimal therapy recommendations for patients.
- This classification will facilitate the enrollment of more homogenous patient populations in clinical trials, aiding the development of effective therapies.
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