WHO classification of CNS tumors

The WHO classification of CNS tumours is the most widely accepted system for classifying CNS tumours, now into its 5^th edition, traditionally published in a blue cover (thus "blue book").

Although traditionally based on histological characteristics of the tumours, since the 2016 revised 4^th edition of the 'blue book' the classification increasingly relies on molecular parameters for classification and in some instances has elevated them above histological features ³.  

Main changes in the 5^th edition (2021)

The 5^th edition (2021) builds on the prior version by placing greater emphasis on molecular markers both in terms of classification and grading and incorporates most of the recommendations made in the cIMPACT-NOW publications ⁶. This approach, however, results in a fairly heterogeneous classification depending on the specific entity. Some tumours remain primarily assessed histologically while others are entirely on the basis of molecular parameters. 

This will be reflected in a "layered report structure" wherein histological features, grading and molecular information will be combined to form an integrated diagnosis.

• integrated diagnosis
• histopathological classification
• CNS WHO grade
• molecular information

Some important changes to terminology and specific entities are worth highlighting. 

Terminology

Type and subtype

• type replaces "entity"
• subtype replaces "variant" 

For example, meningiomas represent one "type" with numerous "subtypes" e.g. chordoid, rhabdoid, clear cell etc.

Grading

Grading within tumour types

Unlike otherOther WHO classification systems thatgenerally grade each tumour based on its own features (iindependently; i.e. the most low-grade version of a particular tumour is given grade 1 regardless of how aggressive it is) relative to other diagnoses.

In contrast, in prior editions of the WHO classification of CNS tumours, entities were graded (roughly) equivalently so that, in principle, grade I tumours of any type were generally indolent and could be cured if completely resected, whereas grade IV tumours would result in rapid demise ⁸.

As a further step towards bringing the CNS classification of tumours in line with those of other systems, this approach has been mostly abandoned, at least aspirationally, abandoned in favour of grading tumours purely within each "type" ⁸.

Due to the inertia of prior classifications and the desire to avoid additional confusion, however, this has only been adopted in a way that does not overly clash with prior grading. For example, despite grading within tumour types, no grade 1 diffuse astrocytoma, IDH-mutant exists (only gradegrades 2, 3 and 4 are available). Similarly, glioblastoma, IDH-wildtype can only ever be a grade 4 tumour ⁸. 

It should also be noted that generally there is shift towards placing less importance on grade as it is often less relevant than location or available therapies. For example, medulloblastoma, WNT activated, despite being a grade 4 tumour, if treated has a good prognosis far better than other medulloblastoma types. 

Arabic numerals

Previously the Roman numerals I, II, III and IV were used for grading. These will be replaced by the Arabic numerals 1, 2, 3 and 4 to bring CNS tumour grades in line with other systems. However, since the features used to grade CNS tumours remain different from those used systemically, it is recommended that the grade be preceded by "CNS WHO", e.g. "meningioma CNS WHO grade 1" ⁸. 

Anaplastic modifier

The term anaplastic, used extensively in the prior classifications has been dropped in favour of grading only. Thus what was previously known as an "anaplastic astrocytoma" is now referred to as an "astrocytoma, IDH-mutant, CNS WHO grade 3" ⁸.

Molecular grading

For the first time, molecular features have been explicitly added to the grading schema, and may supersede histological features. For example, an IDH-wildtype astrocytoma with low-grade histologic features can be considered grade 4 (glioblastoma) in the presence of EGFR amplification, TERT promoter mutation or the combined gain of chromosome 7 and loss of chromosome 10 [+7/-10] ⁸. 

Essential and desirable diagnostic criteria

Each tumour type has been given certain essential diagnostic criteria necessary for a specific diagnosis, as well as additional non-essential but nonetheless desirable criteria ⁸.

Not elsewhere classified (NEC)

In addition to not otherwise specified (NOS), which denotes tumours where complete molecular classification is not available, not elsewhere classified (NEC) has been added to denote tumours that have been fully characterised but that do not fit within the established classification system ^8,9. 

Main changes in the revised 4^th edition (2016)

The 2016 revised 4^th edition significantly changed the classification of a number of tumour families, introducing a greater reliance on molecular markers. The most notable changes involve diffuse gliomas, in which IDH status (mutated vs. wildtype) and 1p19q co-deletion (for oligodendrogliomas) have risen to prominence. Importantly if histological phenotype and genotype are not-concordant (e.g. looks like diffuse astrocytoma but is 1p19q co-deleted, ATRX-wildtype) then genotype wins, and it is used to determine diagnosis ³. 

Medulloblastomas have also been divided into distinct molecular subgroups. 

Another change is the combining of solitary fibrous tumours of the dura with haemangiopericytoma, which although appearing very different on imaging seem now to be manifestations of the same tumour. 

Structure

Despite a move towards molecular markers for some entities, the classification continues to be organised according to the cell of origin (e.g. ependymal tumours) or anatomical origin (e.g. tumours of the sellar region). 

Classification (5^th edition, 2021)​

Gliomas, glioneuronal tumours, and neuronal tumours

Adult-type diffuse gliomas

• astrocytoma, IDH-mutant
• oligodendroglioma, IDH-mutant, and 1p/19q-codeleted
• glioblastoma, IDH-wildtype

Paediatric-type diffuse low-grade gliomas

• diffuse astrocytoma, MYB- or MYBL1-altered
• angiocentric glioma
• polymorphous low-grade neuroepithelial tumour of the young
• diffuse low-grade glioma, MAPK pathway-altered

Paediatric-type diffuse high-grade gliomas

•  diffuse midline glioma, H3 K27-altered
•  diffuse hemispheric glioma, H3 G34-mutant
•  diffuse paediatric-type high-grade glioma, H3-wildtype and IDH-wildtype
•  infant-type hemispheric glioma

Circumscribed astrocytic gliomas

• pilocytic astrocytoma
• high-grade astrocytoma with piloid features
• pleomorphic xanthoastrocytoma
• subependymal giant cell astrocytoma
• chordoid glioma
• astroblastoma, MN1-altered

Glioneuronal and neuronal tumours

• ganglioglioma
• desmoplastic infantile ganglioglioma (DIG) / desmoplastic infantile astrocytoma
• dysembryoplastic neuroepithelial tumour
• diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear clusters (provisional inclusion)
• papillary glioneuronal tumour
• rosette-forming glioneuronal tumour
• myxoid glioneuronal tumour
• diffuse leptomeningeal glioneuronal tumour
• gangliocytoma
• multinodular and vacuolating neuronal tumour
• dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease)
• central neurocytoma
• extraventricular neurocytoma
• cerebellar liponeurocytoma

Ependymal tumours

• supratentorial ependymoma
  • supratentorial ependymoma, ZFTA fusion-positive
  • supratentorial ependymoma, YAP1 fusion-positive
• posterior fossa ependymoma
  • posterior fossa ependymoma, group PFA
  • posterior fossa ependymoma, group PFB
• spinal ependymoma
  • spinal ependymoma, MYCN-amplified
• myxopapillary ependymoma
• subependymoma

Choroid plexus tumours

• choroid plexus papilloma
• atypical choroid plexus papilloma
• choroid plexus carcinoma

Embryonal tumours

Medulloblastoma

• medulloblastomas, molecularly defined
  • medulloblastoma, WNT-activated
  • medulloblastoma, SHH-activated and TP53-wildtype
  • medulloblastoma, SHH-activated and TP53-mutant
  • medulloblastoma, non-WNT/non-SHH
• medulloblastomas, histologically defined

Other CNS embryonal tumours

• atypical teratoid/rhabdoid tumour
• cribriform neuroepithelial tumour (provisional inclusion)
• embryonal tumour with multilayered rosettes (ETMR)
• CNS neuroblastoma, FOXR2-activated
• CNS tumour with BCOR internal tandem duplication
• CNS embryonal tumour

Pineal tumours

• pineocytoma
• pineal parenchymal tumour of intermediate differentiation
• pineoblastoma
• papillary tumour of the pineal region
• desmoplastic myxoid tumour of the pineal region, SMARCB1-mutant

Cranial and paraspinal nerve tumours

• schwannoma and schwannoma (intracranial)
• neurofibroma
• perineurioma
• hybrid nerve sheath tumour
• malignant melanotic nerve sheath tumour
• malignant peripheral nerve sheath tumour
• paraganglioma

Meningiomas

• meningioma

Mesenchymal, non-meningothelial tumours

Soft tissue tumours

• fibroblastic and myofibroblastic tumours
  • solitary fibrous tumour
• vascular tumours
  • haemangiomas and vascular malformations
  • haemangioblastoma
• skeletal muscle tumours
  • rhabdomyosarcoma
• uncertain differentiation
  • intracranial mesenchymal tumour, FET-CREB fusion-positive (provisional inclusion)
  • CIC-rearranged sarcoma
  • primary intracranial sarcoma, DICER1-mutant
  • Ewing sarcoma

Chondro-osseous tumours

• chondrogenic tumours
  • mesenchymal chondrosarcoma
  • chondrosarcoma
• notochordal tumours
  • chordoma (including poorly differentiated chordoma)

Melanocytic tumours

• diffuse meningeal melanocytic neoplasms
  • meningeal melanocytosis
  • meningeal melanomatosis
• circumscribed meningeal melanocytic neoplasms
  • meningeal melanocytoma
  • meningeal melanoma

Hematolymphoid tumours

Lymphomas

• CNS lymphomas
  • primary diffuse large B-cell lymphoma of the CNS
  • immunodeficiency-associated CNS lymphoma
  • lymphomatoid granulomatosis
  • intravascular large B-cell lymphoma
• Miscellaneous rare lymphomas in the CNS
  • MALT lymphoma of the dura
  • other low-grade B-cell lymphomas of the CNS
  • anaplastic large cell lymphoma (ALK+/ALK−)
  • T-cell and NK/T-cell lymphomas

Histiocytic tumours

• Erdheim-Chester disease
• Rosai-Dorfman disease
• juvenile xanthogranuloma
• Langerhans cell histiocytosis
• histiocytic sarcoma

Germ cell tumours

• mature teratoma
• immature teratoma
• teratoma with somatic-type malignancy
• germinoma
• embryonal carcinoma
• yolk sac tumour
• choriocarcinoma
• mixed germ cell tumour

Tumours of the sellar region

• adamantinomatous craniopharyngioma
• papillary craniopharyngioma
• pituicytoma, granular cell tumour of the sellar region, and spindle cell oncocytoma
• pituitary adenoma (pitNET)
• pituitary blastoma

Metastases to the CNS

• metastases to the brain and spinal cord parenchyma
• metastases to the meninges

History and etymology

The International Agency for Research on Cancer (IARC) is the specialised cancer agency of the World Health Organisation and commissions and publishes the "WHO classification of tumours" series. Please note that the term "blue book" is used for all books in the series not just the CNS tumour book ¹⁰.