Molecular Pathology Diagnostic Service

Click here for the list of Molecular Pathology UKAS accredited Assays

Introduction to The Molecular Pathology Diagnostic Service

The discipline of Molecular Pathology encompasses those investigations which determine the diagnostic, prognostic and predictive profile of pathology specimens through the analysis of alterations to DNA, RNA or-in certain cases-Proteins. This can include small mutations or large chromosomal aberrations, DNA methylation, and changes to RNA transcription and protein expression levels.

Service Background

The Molecular Pathology Diagnostic Service (MPDS) provides a diagnostic molecular pathology service to internal users within the Trust, external users regional; national and international. The department processes over 20,000 samples per year and offers services in both solid tumour testing and circulating tumour DNA.

The department utilizes a broad range of molecular techniques including immunohistochemistry, FISH, PCR based targeted assays (Sanger Sequencing, real time PCR, pyrosequencing) and next generation sequencing (NGS) to provide testing for protein expression, gene mutation, gene methylation, gene amplification and chromosome translocation. 

The laboratory is accredited to ISO 15189:2012. Tests that fall under this scope can be found using the link above and is also indicted in the 'Test Repertoire' section below.

The department of Molecular Pathology is part of Clinical Laboratory Services and operates within the Quality Management System of the Clinical Laboratory Services, it is led by a Consultant Clinical Service Lead, a Principal Clinical Scientist and an Operations Manager. MPDS participates fully in UK NEQAS and GENQA External Quality Assurance schemes where appropriate.

MPDS provides a comprehensive molecular pathology service to the Trust, and nationally, between 8:30 and 17:00 Monday - Friday. Please contact the laboratory for any pricing enquiries.

Contacting The Laboratory

Several key personnel are involved with the management of the department at QEHB. For general enquiries, please contact the Specimen Reception.

Clinical Service Lead
  Dr Philippe Taniere
Principal Clinical Scientist
Dr Matthew Smith
Molecular Operations Manager
Brendan O'Sullivan
Quality Lead
Helen Stokes
Molecular Specimen Reception

Requesting a Test

In order to process specimens efficiently, it is essential that request forms are fully completed in a clear and legible format. The use of patient ID stickers is permitted however please ensure you use the full patient sticker NOT the smaller blood tube sticker. All specimens received into MPDS must meet the agreed laboratory minimum data set; any specimens not meeting the criteria may be returned to the requesting department. Please ensure that any important information (e.g. clinical history, etc.) is clearly indicated on the form and ensure that any priority or urgent cases are marked as such.

Click the link below to view and download the latest versions of our request forms.

Molecular Testing Request Forms

Minimum Data set Required

Data on the request form and the specimen must be compatible. All specimens must carry a minimum, legible and compatible data-set on both the request form and the specimen label. Where possible a copy of the pathology report should be provided.

Patient Data Item Request Form Specimen
Forename (not just initials)  
Date of Birth  
Hospital ID &/or NHS number  
Block ID
Report Destination  
Requesting Practitioner  
Consultant (if different from above)  
Clinical Details  
Date sample sent  
Specimen type (& site if appropriate)  
Investigations required  

Sending Samples To Us & Subsequent Return of Material

For information on how to send samples to MPDS including packaging and transport, and information on the return of samples, please click here.

Molecular Test Repertoire & Turnaround Times

Breast Cancers

The section offers a comprehensive HER2 analysis service for breast cancers. Immunohistochemistry, with the Roche/Ventana 4B5 antibody, is used to screen patients for expression levels of the HER2 protein and identify those “over-expressers” who are most likely to benefit from treatment with Trastuzumab (Herceptin). Where expression levels are equivocal, FISH is used to determine amplification at the gene level. Service users may access the full service, or submit cases for FISH analysis only if performing their own IHC.

Gastric Cancers

As with breast cancers, HER2 analysis is performed in Gastric cancers to assist in predicting which therapies patients will benefit from. As well as this standard-of-care testing, mismatch-repair analysis and ISH for EBV are also available on demand.

Colorectal Cancers

RAS (KRAS and NRAS) mutations confer resistance to anti-EGFR monoclonal antibodies, and act as a negative predictive marker for these therapies.  The National Institute for Clinical Excellence (NICE) has approved the use of Cetuximab and Panitumumab for the treatment of metastatic colorectal cancer in patients who carry normal, “wild-type” RAS genes. RAS testing is mandatory prior to their prescription.

BRAF gene mutation analysis is provided on demand for colorectal cancer patients. This can be used to inform patient management or, in combination with mismatch repair expression (see below), to help establish the presence of the inherited cancer syndrome HNPCC (Lynch syndrome).

We are a reference centre for Mismatch repair (MMR) protein expression analysis in patients suspected to have Lynch syndrome; we test over 700 cases a year. immunohistochemical testing allows identification of patients without normal DNA repair processes, who are therefore more likely to have Lynch syndrome. In patients with MLH1 loss we can also perform reflex testing for BRAF V600E mutations and MLH1 promoter methylation status. Mismatch repair protein expression is also requested increasingly to help inform patient chemotherapy decisions, as patients lacking MMR expression appear to have reduced sensitivity to certain cytotoxic treatments.

BRAF p.Val600Glu (“V600E”) specific immunohistochemistry (IHC) is available on demand.

Lung Cancers

EGFR mutations correlate with the effectiveness of certain Tyrosine Kinase Inhibitors (TKIs) such as Gefitinib, Erlotinib, Afatinib, and Osimertinib against some Non-Small Cell Lung Cancers (NSCLCs). Activating mutations are reported to correlate with significant responses to such treatment, whilst certain other mutations correlate with resistance to first- and second-generation TKIs, but predict response to newer agents. EGFR mutation status is therefore vital in deciding the most appropriate treatment regime. The service also offers EGFR analysis on circulating tumour DNA extracted from plasma. This is of particular use in testing patients for acquired, targetable secondary mutations when they begin to progress whilst on treatment that targets their primary EGFR mutation. It may also function as a surrogate where clinical circumstances make obtaining a more representative tissue specimen for initial diagnostic testing difficult or impossible. The service can provide specialised collection tubes for users wishing to submit samples.

Anaplastic lymphoma kinase (ALK) gene fusions can be targeted with specific inhibitors, and translocation analysis using immunohistochemistry or Fluorescence In-Situ Hybridisation (FISH) is now standard alongside EGFR mutation analysis to determine 1st line treatment for lung NSCLC. In addition to ALK analysis, the service provides FISH and IHC testing for ROS1 fusions in lung cancer. 

PD-L1 expression analysis is also important in informing first (and second) line anti PD-1 / anti-PD-L1 monoclonal antibody treatment for lung NSCLC. A relatively recent addition to the testing landscape, in 2016, immunohistochemical analysis using companion-diagnostic antibodies specific to the relevant treatments gives a quantitative expression result.

Gastrointestinal Stromal Tumours (GIST)

Up to 90% of all malignant GISTs harbour gain-of function mutations in the KIT / PDGFRA genes. Primary mutations have been described in exons 8, 9, 11, 13 & 17 of KIT, and exons 12, 14 & 18 of PDGFRA. Secondary (acquired or treatment associated) mutations have also been described. Selective TKIs have a high response rate in patients with advanced GISTs, which are largely radiotherapy and chemotherapy resistant. Evidence suggests that the type and location of KIT or PDGFRA mutations in GISTs predicts the response to TKI treatment.


The BRAF gene is frequently mutated in human melanomas, with mutations seen in 35-50% of cases. Mutations lead to constitutive activation and aberrant signalling, and subsequent malignant behaviour. Drugs that treat those cancers by inhibiting BRAF are now licensed for use in metastatic disease.

The NRAS gene is also frequently mutated in melanoma; between 10-20% of tumours show an NRAS mutation, and these are thought to be mutually exclusive with alterations in BRAF. NRAS testing is offered as a supporting aid in selecting patients for access to novel therapeutic interventions or clinical trials targeting the pathway activated by mutant NRAS.

Mutations in the KIT gene are seen in Acral and mucosal melanomas and represent potential therapeutic targets.

PD-1 and PD-L1 inhibition, particularly in combination with anti-CTLA4 therapies, has shown profound and sustained effects against metastatic melanoma. Whilst PD-L1 expression analysis is not mandatory for prescription, as it is with some lung NSCLC therapies, it has been shown to be helpful in informing decisions on whether to use mono- or combination-therapy.

Brain Tumours

The revision of the WHO classification of CNS tumours in 2016 has expanded the range of essential and desirable molecular analyses performed.

Epigenetic silencing of the MGMT (O6-methylguanine–DNA methyltransferase) gene by promoter methylation is associated with longer overall survival in patients with glioblastoma who, in addition to radiotherapy, received alkylating chemotherapy with temozolomide. High levels of MGMT activity in cancer cells create a resistant phenotype by hindering the therapeutic effect of alkylating agents and may be an important determinant of treatment failure.

Combined loss of chromosome arms 1p and 19q (denoted as 1p-/19q-) is a powerful predictor of chemotherapeutic response and survival in oligodendrogliomas. A FISH based analysis of these loci is available as a tool to assist patient management. More recently it has been employed diagnostically in the differentiation of ATRX-positive Oligodendrogliomas and Astrocytomas.

Mutation analysis of the IDH1 and IDH2 genes is used as a supplement to immunohistochemistry. Whilst the IDH1 R132H-specific antibody detects the majority of IDH mutated tumours, mutation analysis for rarer R132 variants along with IDH R100 and IDH2 R172 mutations is used in particular relevant clinical scenarios.

Turnaround Times

Turnaround Times from sample receipt to result issued are variable dependent on the test requested.

 Test Quoted Turnaround time (working days)  Assays currently included in our application for ISO15189:2012 accreditation scope
ALK translocation testing by FISH >90% in 7-10 days Yes
ALK translocation testing by IHC >90% in 5-7 days Yes
BRAF V600 mutation testing  >90% in 5-7 days Yes 
COL1A1-PDGFb FISH  >90% in 7-12 days  No
EBERS ISH  >90% in 5-7 days  No
EGFR (Exon 18-21 mutations) & ALK IHC  >90% in 5-7 days  Yes 
EGFR plasma mutation testing (Exon 18-21 mutations)  >90% in 5-7 days  Yes 
EGFR tissue mutation testing (Exon 18-21 mutations) >90% in 5-7 days  Yes 
HER-2 testing (FISH) >90% in 7-12 days  Yes 
HER-2 testing (IHC) >90% in 7-12 days  Yes
IDH1 (codon 132) /IDH2 (codon 172) please contact laboratory Submitted for ETS July 2019
KIT (8,9,11,13,17), PDGFRa (12,14,18) testing by Sanger Sequencing (1-2 exons) >90% in 7-15 days Capillary sequencing method; submitted for ETS July 2019. On scope by NGS targeted panel.
KIT (8,9,11,13,17), PDGFRa (12,14,18) testing by Sanger Sequencing (3+ exons) >90% in 15-30 days Capillary sequencing method; submitted for ETS July 2019. On scope by NGS targeted panel.
KRAS testing (codons 12,13,117,61,146) >90% in 5-7 days Yes
MDM2 amplification (FISH) >90% in 7-12 days Submitted for ETS July 2019
MGMT promoter methylation >90% in 7-10 days Yes
MLH promoter hypermethylation >90% in 7-10 days Yes
MMR testing by IHC >90% in 7-10 days Yes (provided by the QEHB Cellular Pathology department, under terms of MOU for service provision)
N/KRAS testing (KRAS codons 12,13,61,117,146 and NRAS 12,13,61) >90% in 7-10 days Yes
Next Generation Sequencing (Hotspot panel (KRAS, NRAS, IDH1, IDH2, BRAF, EGFR, KIT, PDGFRA) please contact laboratory Yes
NRAS testing (codons 12,13,61) >90% in 5-7 days  Yes
PD-L1 (Agilent 22C3 assay) >90% in 5-7 days  Yes
PD-L1 (Agilent 28-8 assay) >90% in 5-7 days  Submitted for ETS July 2019
PD-L1 (Roche SP142 assay)  >90% in 5-7 days  Submitted for ETS July 2019
ROS testing (FISH) >90% in 7-10 days Submitted for ETS July 2019
ROS testing (IHC) >90% in 5-7 days  Yes
SS18 FISH >90% in 7-12 days No
1p/19q co-deletion analysis >90% in 7-12 days Submitted for ETS July 2019


Specimens are reported on the Laboratory Information Management System. For internal patients the reports are then automatically uploaded to the Clinical Portal For external users, reporting is provided electronically. A list of recipients and email addresses is required. All reports are stored with the laboratory LIMS system indefinitely.

The department will not send reports by Faxitron.

Members of MPDS are available from 08:30 – 17:00 Monday – Friday for the reporting of specimens and to offer advice. 


UHB, Department of Cellular Pathology, Department of Molecular Pathology, Cancer Testing, Molecular, Molecular Diagnostic, Lung Cancer, PDL1, EGFR, ROS, ALK, HER2, RAS, KRAS, NRAS

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