Your browser doesn't support javascript.
loading
ATRX immunohistochemistry can help refine 'not elsewhere classified' categorisation for grade II/III gliomas.
Burford, C; Laxton, R; Sidhu, Z; Aizpurua, M; King, A; Bodi, I; Ashkan, K; Al-Sarraj, S.
Affiliation
  • Burford C; Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London , London , UK.
  • Laxton R; Department of Neuropathology, King's College Hospital , London , UK.
  • Sidhu Z; Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London , London , UK.
  • Aizpurua M; Department of Neuropathology, King's College Hospital , London , UK.
  • King A; Department of Neuropathology, King's College Hospital , London , UK.
  • Bodi I; Department of Neuropathology, King's College Hospital , London , UK.
  • Ashkan K; Department of Neurosurgery, King's College Hospital , London , UK.
  • Al-Sarraj S; Department of Neuropathology, King's College Hospital , London , UK.
Br J Neurosurg ; 33(5): 536-540, 2019 Oct.
Article in En | MEDLINE | ID: mdl-31018710
ABSTRACT

Purpose:

The 2016 WHO tumour classification highlights the role of IDH1/2 gene mutation and 1p/19q co-deletion in classifying grade II/III gliomas. A recent cIMPACT-NOW update proposes the use of the term 'Not Elsewhere Classified' (NEC) for IDH-mutant, non co-deleted tumours. Here we show how the incorporation of ATRX immunohistochemistry can be used to better delineate the NEC group.

Methods:

Clinical data was collected for 112 patients (59% male) treated at our unit. Mutations in IDH1/2 genes were detected by pyrosequencing or immunohistochemistry, 1p/19q co-deletion was assessed with fluorescence in situ hybridisation and ATRX status was determined using immunohistochemical techniques. Tumours were grouped on the basis of molecular markers and outcomes compared.

Results:

The mean age of diagnosis was 42.6 years (20-73 years). There were 88 oligodendrogliomas (II = 47, III = 41), 18 diffuse astrocytomas (II = 9, III = 9) and 6 oligoastrocytomas (II = 4, III = 2). The majority of gliomas (87.5%) had mutations in IDH1/2. 1p/19q co-deletion was significantly associated with oligodendroglial morphology (p = < 0.001) and was mutually exclusive with ATRX mutation. Classification on the basis of molecular information showed a significant different in survival between the groups.

Conclusions:

ATRX immunohistochemisty is a useful adjunct which can be used with IDH mutation status, 1p/19q co-deletion and histological findings to further define tumour groups. More work is needed to understand the molecular profiles and prognostic implications for non co-deletion, ATRX preserved cases.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligodendroglioma / Astrocytoma / Brain Neoplasms / X-linked Nuclear Protein / Mutation Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Br J Neurosurg Journal subject: NEUROCIRURGIA Year: 2019 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligodendroglioma / Astrocytoma / Brain Neoplasms / X-linked Nuclear Protein / Mutation Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Br J Neurosurg Journal subject: NEUROCIRURGIA Year: 2019 Document type: Article Affiliation country: Reino Unido
...