We are offering a large spectrum of molecular tests relevant to the diagnosis or prognostication of brain tumours. These tests either aid the histological diagnosis of brain tumours or are essential for planning enrolment into clinical trials or to decide for the optimum therapy. We offer the tests to all NHS (price see below) and private hospitals. Price list at the end of this website.
Important: This request form is updated regularly. It is valid only on the day of download. Please regularly download new copies of this form
Further inquiries about our services and referrals:
Prof Sebastian Brandner
Dr Zane Jaunmuktane
Dr Ashirwad Merve
Technical inquiries, specimen submission:
Phone (office) 020 3448 4243
Andrew Lowe, senior bioinformatics scientist
Molecular test portfolio for gliomas
The main differential diagnosis of gliomas is to distinguish astrocytomas, oligodendrogliomas and IDH wild-type glioblastoma. These require a set of markers which we offer as "package". This allows us to return a precise integrated diagnosis which combines histological assessment, immunohistochemical testing with established biomarkers, supplemented with the molecular tests which assess point mutations and chromosomal losses and gains.
Characteristic patterns of DNA methylation of CpG islands in the genome are key features in various tumours. The Illumina 850k EPIC array assesses the DNA methylation status of a small proportion of the 850,000 individual CpG sites on the array. An algorithm, developed at the DKFZ in Heidelberg, Germany, is able to distinguish brain tumour entities based on their methylation profile. It is currently based on over 10,000 reference brain tumour cases and is periodically updated.
Guidance when to use the classifier: in adult brain tumours, we recommend using the classifier for all histologically unclear CNS neoplasms. In particular, when a basic molecular pathology workup, for example using the above markers, does not yield diagnostically relevant results.
As an informal (i.e. not evidence-based) practical guidance, we consider using the Illumina array when a CNS neoplasm cannot be diagnosed with approximately 8-10 immunostains, and/or with any of the above tests.
With small biopsies, we recommend considering the Illumina array well before the tissue is exhausted.
The following table lists typical examples of possible combinations of tests and their minimum cost. All prices are "Provider-to-Provider" between NHS Trusts. The prices include interpretation and evaluation of the neoplasms in the context of the referred diagnosis, our own opinion based on H&E and the molecular test result. For a formal opinion on the histological diagnosis, we recommend referral with all IHC Slides and a specific request in the referral letter, but please also use our referral form.
The prices are for guidance only and can vary depending on the number of blocks referred, extent of consultation and repeat tests due to reduced sample quality. Referral of multiple blocks can increase the cost of our tests.
Molecular analysis of LOH1p/19q in astrocytomas and oligodendrogliomas
Relevance: Loss of 1p/19q is a feature of Oligodendrogliomas. 1p/19q loss is an early event in oligodendroglioma and is retained during tumour progression.
The combined loss of 1p/19q is related to survival. This improved prognosis is present whether observed at initial diagnosis or at recurrence. 1p/19q loss oligodendrogliomas also progress more slowly at recurrence.
CDKN2A/B homozygous deletion is a prognostic marker for IDH-mutant astrocytomas. A deletion indicates more rapid progression and recurrence.
This test is done in conjunction with copy number assays for 7p (EGFR locus), and sequencing of the following genes: IDH1/IDH2, Histone H3.3 (G34 and K27), BRAF and TERT promoter.
Histological assessment, and IHC for IDH1R132H, ATRX and Ki67
Copy Number Assay with Real-Time PCR; Sanger sequencing
Price: See list below.
Molecular analysis of EGFR amplification and EGFRvIII mutations
EGFR: Copy Number Assay with Real-Time PCR. If EGFR is not amplified, EGFRvIII will not be tested
- EGFR amplification: Approximately 50% of GBMs are characterised by overexpression of EGFR and EGFR gene amplification.
- EGFRvIII enhances the tumourigenic potential of GBM by activating and sustaining mitogenic, anti-apoptotic and pro-invasive signalling pathways. EGFRvIII is a tumour-specific mutation that is widely expressed in GBM and other neoplasms, resulting from an in-frame deletion of 801 bp spanning exons 2 to 7 of the coding region of EGFR. This in-frame deletion mutation splits a codon, resulting in a novel glycine at the fusion junction producing a tumour-specific epitope target for cellular or humoral immunotherapy.
EGFR: Copy Number Assay with Real-Time PCR.
EGFRvIII mutations: RNA isolation from Paraffin sections, Reverse transcription and detection of the fusion gene by Sequencing.
BRAF fusion gene and V600E point mutations
Relevance: The identification of the BRAF a fusion gene (A tandem duplication occurring at 7q34 leading to a fusion between KIAA1549 and BRAF genes) in more than 60% of Pilocytic astrocytomas, but not in morphologically similar neoplasms or in reaction lesions is used for molecular diagnostics for PA. The BRAF gene resides on chromosome 7q, near the HIPK2 locus and has been linked to numerous other cancers.
The V600E mutation is located in exon 15 of the BRAF gene. 66% WHO grade II pleomorphic xanthoastrocytomas and WHO grade III PXA with anaplasia, 18% of WHO grade I gangliogliomas and in 9% pilocytic astrocytomas (strongly associated with extra-cerebellar location). This makes the V600E test a useful diagnostic marker for these.
BRAF Fusion: RNA isolation from Paraffin sections, Reverse transcription and detection of the fusion gene by Sequencing.
Price: See list below
Methylation of the MGMT promoter in gliomas
Test Method: Methylation sensitive High-Resolution Melting (MS-HRM) analysis.
Relevance: MGMT (O6-methylguanine DNA methyltransferase) is a key enzyme in the DNA repair network. MGMT removes the mutagenic and cytotoxic adducts from O6 guanine in DNA, the preferred point of attack of alkylating chemotherapeutic agents (i.e. BCNU, temozolomide, etc). Hypermethylation of the CpG island located in the promoter region of MGMT is primarily responsible for the loss of MGMT function in many tumour types. MGMT hypermethylation alone, without treatment with an alkylating agent, is a negative prognostic marker. MGMT hypermethylated tumours are more sensitive to the killing effects of alkylating drugs used in chemotherapy.
Price: See list below
|Tests||NHS-E Test directory||Method||Price (£)|
|IDH1, IDH2, Histone H3.3, TERT, BRAF||M29.1||Sequencing||100|
|Histone H1H3B, H1H3C, H2H3C, H3F3A||M191.1||Sequencing||100|
|MGMT promoter methylation||M27.6||MS-HRM PCR||185|
|1p/19q, 7p/EGFR, CDKN2A/B, IDH1, IDH2, Histone H3.3, TERT, BRAF||M192.1, M192.11||qPCR, Sequencing||235|
|1p/19q, 7p/EGFR, CDKN2A/B, IDH1, IDH2, Histone H3.3, TERT, BRAF, MGMT||M192.1, M192.11, 192.17||qPCR, Sequencing, HRM-PCR||300|
|EGFR amplification and vIII mutation||M28.2, M192.15||qPCR, RT-PCR||240|
|BRAF V600E only||M35.1||Sequencing||85|
|BRAF V600E and BRAF:KIAA fusion||M35.1, M36.1||Sequencing and RT-PCR||285|
|Illumina 850k EPIC Methylation array||Expected June 2021||Methylation array, analysis with classifier algorithm, developed at DKFZ in Heidelberg Turnaround: 2-6 weeks.||495|
HRM PCR: High-resolution Melt PCR