Determining the HER2 status of breast carcinomas is a prerequisite for the use of the monoclonal antibody trastuzumab (Herceptin®), which has recently been licensed for the treatment of metastatic disease. This necessitates a test based on archival material. The preferred analyses are immunohistochemistry with fluorescent in situ hybridisation (FISH) as a follow up test for ambiguous results. Guidelines have been developed for standardised, well controlled procedures for the provision of reliable results. A group of three reference laboratories has been established to provide advice, quality assurance, and materials, where needed.
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The humanised anti-HER-2/neu (also known as c-erbB-2, further denoted HER2) monoclonal antibody trastuzumab (Herceptin®) can be used to treat women with HER2 positive metastatic breast cancer.1 Establishing tumour HER2 status is a prerequisite for the use of trastuzumab.2 However, a widely accepted and standardised test for HER2 status is not currently available.3 These recommendations have been designed to give notice of the availability of a reference laboratory service and to give advice on methodology for local testing to ensure that HER2 testing results are accurate and reliable, regardless of the test that is used.
Formalin fixed, paraffin wax embedded tumour tissue samples are appropriate for assay.4 Other methods of tissue fixation can adversely affect reactivity.
APPROPRIATE LABORATORY ASSAY METHODS
Immunohistochemistry (IHC) and fluorescent in situ hybridisation (FISH)5 are the techniques recommended for determining HER2 status. We do not intend to be prescriptive about methodology or the antibodies suitable for ICH because there is no substantive evidence to support the exclusive use of one IHC testing method or reagent. For immunohistochemical HER2 testing, comprehensive standardisation of methodology and the inclusion of validated controls are mandatory. The HercepTest® meets these criteria, but owing to cost considerations, other IHC tests and antibodies other than the polyclonal antiserum used in this test may be used (see recommendations regarding the use of controls and test validation below).
FISH testing for HER2 should meet the following criteria: (1) the inclusion of a chromosome 17 control to allow for correction of the HER2 signal number for chromosome 17 aneusomy (seen in over 50% of cases); (2) comprehensive standardisation of methodology; and (3) validated controls. Although there are several commercial systems available for FISH HER2 testing, the PathVysion® assay (Vysis, Richmond, Surrey, UK) is recommended for diagnostic testing because it meets the above criteria. Owing to cost considerations, other probes and in house prepared probes may be use, but care must be taken to ensure that these are correctly validated (see recommendations below).
Currently, the other available HER2 testing techniques (polymerase chain reaction, enzyme linked immunosorbent assay, Southern blotting) should be used for research only. Standard protocols should be developed and applied for local IHC or FISH HER2 tests. These should be validated using standardised commercial kit assays or local assay methodologies that have been validated against the well characterised tissue sets that are available from the reference laboratories (see below).
The inclusion of controls of known HER2 status in all HER2 tests is required to ensure test accuracy. One positive and one negative control of known immunoreactivity and gene signal number are recommended as a minimum; controls producing results close to important decision making points should also be considered.
The reference laboratories can validate locally produced controls by FISH and HercepTest if required.
Tissue array blocks containing multiple tissue samples of known HER2 status characterised by FISH and IHC are being developed by the reference laboratories to facilitate test validation.
FOR ALL IHC TESTS
Antigen retrieval processes should be standardised and follow strict protocols. The antibody used and its titre should be predefined. No single antibody has been consistently demonstrated to be superior in terms of specificity and sensitivity. At present, antibodies CB11 (Novocastra, Newcastle Upon Tyne, UK), TAB 250 (Zymed, San Francisco, California, USA), and A0485 (Dako, Ely, Cambridgeshire, UK) are the most widely used. Test conditions (temperature, exposure time, etc) should be standardised.
There is evidence that HER2 protein reactivity may deteriorate in fixed paraffin wax sections over a period of months. It is recommended that control block sections are prepared fresh or that storage time is restricted to < 3 months unless testing to assess degradation has been conducted.
Test conditions should be optimised so that distinct moderate or strong membrane staining identifies FISH positive samples.
Laboratories not wishing to standardise in house methodology should consider using a commercial kit assay system such as the HercepTest.
Excessive antigen retrieval can be monitored by an evaluation of normal breast epithelial cells as an internal control. Should membrane reactivity be identified in the normal cell population, excessive antigen retrieval may have occurred. It is recommended that the assay be rejected and retested. Alternatively, some groups have recommended that scoring of the tumour cell population be modified by subtracting the degree of normal cell reactivity.
Only membrane staining of the invasive tumour should be considered when scoring IHC tests.
If the HercepTest is used, it is recommended that laboratories adhere strictly to the kit assay protocol and scoring methodology. Local modifications of techniques can lead to false positive and negative assay results. The scoring method provided with the kit uses a semi-quantitative system based on the intensity and percentage of positive cells, giving a score range of 0 to 3+. Samples scoring 3+ are regarded as unequivocally positive and 0/1+ as negative. Borderline 1+/2+ and 2+ require confirmation using another analysis system, preferably FISH.
Until there is more evidence based on patient response to treatment, we recommend using the HercepTest scoring method for tumours assessed using other IHC methods. We anticipate that simplified IHC scoring methods will be developed. For example, cases should be reported as positive for HER2 overexpression if > 10% of cells show moderate or strong complete membrane staining; cases that show equivocal/borderline reactivity should be retested, preferably using FISH.
Interobserver variation in the assessment of staining can lead to misclassification of HER2 status. Each individual should standardise scoring against known positive, negative, and borderline cases.
Laboratories offering an IHC service are advised to participate in the UK NEQAS Immunohistochemistry External Quality Assurance (EQA) scheme.
Fluorescence in situ hybridisation (FISH)
The Vysis PathVysion kit is recommended if FISH is performed because it meets the above mentioned criteria for proper HER2 FISH testing, with results being expressed as the ratio of HER2 signal to chromosome 17 signal. Tumours showing a ratio of > 2 should be considered positive. Cut off values for HER2 gene amplification when chromosome 17 probes are not used have not been established.
FOR ALL FISH TESTS
There is no evidence that storage of blocks or slides leads to deterioration of signal. However, storage of cut sections from controls or samples for over six to 12 months should be avoided.
It is advisable to locate areas of invasive tumour using a serial section stained with haematoxylin and eosin and to use this to locate tumour areas to be scored after testing. Care should be taken to avoid areas of ductal carcinoma in situ, which can show amplification even where adjacent invasive tumour cells are negative.
Tissue digestion should be standardised to maintain nuclear morphology and should follow strict protocols. Nuclear structure should be evaluated before hybridisation and digestion, where appropriate, to preserve nuclear integrity. Hybridisation and washing steps should be standardised. Guidance can be provided by the reference laboratories.
It is recommended that commercially available probes are used. For systems using in house nick translated probes, attention should be given to batch variability of nick translation enzymes, etc.
Laboratories not wishing to use in house methods should consider using a commercial system such as the Vysis PathVysion kit.
For all test systems, the scoring protocol included in the PathVysion kit is recommended. The number of chromosome 17 and HER2 signals is scored for 60 cells, where possible from three distinct tumour fields, and the mean HER2 to chromosome 17 copy ratio is calculated. Where tumour heterogeneity is seen (1–2% of cases), more cells from the amplified regions should be scored. Samples with > 2.0 copies of HER2 for each chromosome 17 are considered to be amplified.
Interobserver variation should be assessed until good reproducibility is attained. For non-amplified samples, interobserver variation should be between 10% and 15%. Variation increases with highly amplified samples, but is not critical where the ratio exceeds 4.
To ensure adequate quality assurance, UK laboratories wishing to set up independent FISH testing are recommended to join the reference laboratories' EQA scheme.
Reference laboratory service
For the UK, three HER2 testing reference laboratories have been established in London, Nottingham, and Glasgow.
• Professor Mitch Dowsett, Department of Biochemistry, The Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK.
• Dr Ian Ellis, Department of Histopathology, City Hospital, Hucknall Road, Nottingham NG5 1PB, UK.
• Dr John Bartlett, University Department of Surgery, Glasgow Royal Infirmary, Level II, Queen Elizabeth Building, Alexandra Parade, Glasgow G31 2ER, UK.
These laboratories use validated IHC (HercepTest) and FISH techniques (PathVysion) to establish HER2 status, and also run an interlaboratory quality assurance scheme.
The service provided by the reference laboratories is available to all laboratories for advice and testing of HER2 status.
Test results will be provided within two weeks of sending to the reference laboratories. Laboratories that require data sooner or have in house procedures should conduct their testing according to the above guidelines.
Similar initiatives are expected in other countries where trastuzumab treatment is used.
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