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J Clin Pathol. 2007 September; 60(9): 1067–1068.
Published online 2007 February 5. doi:  10.1136/jcp.2006.043356
PMCID: PMC1972421

Chromogenic in situ hybridisation (CISH) should be an accepted method in the routine diagnostic evaluation of HER2 status in breast cancer

HER2 protein overexpression or gene amplification is detected in approximately 20% of breast tumours, is associated with an aggressive phenotype and is predictive of response to trastuzumab therapy. The use of chromogenic in situ hybridisation (CISH) for evaluating HER2 status routinely is recognised in much of Europe but has yet to achieve widespread acceptance in the UK. CISH analysis for HER2 status was performed on 161 breast cancer cases. Results were compared with immunohistochemistry (IHC) and dual‐colour fluorescence in situ hybridisation (FISH) data. There was 100% concordance between CISH and FISH, but only 93.8% concordance between CISH and IHC. Performing CISH ‘in‐house' was found to cost approximately 50% less than the FISH/IHC protocol at the reference laboratory. It is concluded that CISH is as accurate as FISH for diagnostic purposes and is more cost‐effective than the IHC/FISH regimen currently favoured in the UK.1

Recent data show that amplification of the HER‐2 gene is the most reliable predictor of response to trastuzumab therapy,2 indicating that a gene‐based assay, rather than a protein overexpression assay, would be the most suitable type of analysis for HER2 status in breast tumour samples.

With the recent change in the licensing of trastuzumab to include its use as an adjuvant therapy (NICE 2006), it is important that patients most likely to benefit from its use are accurately identified. This change in the use of trastuzumab has increased the workload of histopathology laboratories significantly as well as creating an additional financial burden for hospital Trusts. We investigated the possibility of setting up HER2 analysis within our pathology department. Chromogenic in situ hybridisation (CISH), like fluorescence in situ hybridisation (FISH), directly visualises the number of gene copies present in the nucleus, it is cheaper and it produces a permanent record of the slide that can be interpreted with a light microscope in the context of the tumour histopathology. CISH and FISH have been compared for their sensitivity and specificity in numerous previous reports from across Europe,3,4,5,6,7 but CISH is not widely used in the UK.1 The current study was done as a validation study prior to setting up a HER2 testing service using CISH, but it was felt that our experience may be of interest to other laboratories considering setting up their own HER2 testing service.

Methods

One hundred and sixty‐one breast cancer cases for which material was obtainable and that had immunohistochemistry (IHC) and/or FISH data available were chosen for the study. The samples had been analysed by the DAKO HercepTest IHC (DakoCytomation, Ely, Cambridgeshire, UK) and a small number of them (n = 24) had required confirmation by PathVysion dual‐colour FISH (Abbott UK, Queensborough, Kent, UK) mostly because they were IHC 2+. The manufacturer's protocols and scoring systems for both procedures were followed. The same cases were subsequently examined using a commercially available CISH assay (Zymed, Invitrogen, Paisley, UK), and the manufacturer's protocol was followed. The resulting slides were examined independently by two pathologists using light microscopy. The areas of invasive tumour were identified and the HER2 status was scored using the manufacturer's guidelines. Amplification was recorded when the nuclei of >50% cells contained clusters, multiple dots (>5) or a mixture of both. No amplification was recorded when the nuclei of >50% cells contained one or two small dots. At least four areas of the tumour were examined to overcome issues of heterogeneity. Samples with 3–5 and 5–10 dots were further analysed using a chromosome 17 centromeric probe to confirm highly proliferating tumours in the former and cases of chromosome 17 numerical aberration in the latter. The cost implications for both the protocols were assessed.

Results

Results were obtained for all 161 samples tested. Amplified and non‐amplified cases were readily distinguishable in the majority of cases (fig 11),), whilst chromosome 17 correction was required in 19 cases (10.6%) to confirm interpretation.

figure cp43356.f1
Figure 1 (A) Core biopsy of invasive ductal carcinoma. Cells have been hybridised with a HER2 gene probe and visualised using an anti‐digoxigenin peroxidase antibody, developed with 3',3'‐diaminobenzidine. Chromogenic in situ hybridisation ...

CISH and IHC showed 93.8% concordance (151/161) (table 11).). Dual‐colour FISH and CISH showed 100% concordance (table 11).). There were seven (4.4%) IHC 3+ cases that were found by CISH to be not amplified. In each one of these seven cases, the results obtained with CISH were re‐confirmed by dual‐colour FISH analysis. One case (0.6%), originally scored IHC 1+, showed amplification by CISH, again re‐confirmed by dual‐colour FISH. There was 100% agreement between the two examining pathologists.

Table thumbnail
Table 1 HER2 1HC and FISH versus CISH data

Discussion

FDA (Food and Drug Administration) approved HercepTest IHC analysis has been adopted as the frontline test for identifying patients eligible for trastuzumab therapy. A total of 5% of the samples in our series did not show the expected correspondence between HER2 gene status and HER2 protein expression, similar to previous reports.4,8 Our data indicate that 11% of women eligible for trastuzumab therapy on the basis of the IHC result are unlikely to benefit from it.

Take‐home messages

  • Use of an in situ hybridisation assay in place of immunohistochemsitry would identify more accurately those women who would benefit from trastuzumab therapy.
  • Chromogenic in situ hybridisation (CISH) is as sensitive and as specific as fluorescence in situ hybridisation (FISH)
  • CISH is more cost‐effective than FISH

Misdirected therapy will potentially cost health authorities significant sums of money. A recent cost‐effectiveness analysis for HER2 testing and trastuzumab therapy9 concluded that it is more cost‐effective to use FISH alone or as confirmation of all IHC 2+ and 3+ results, rather than the current system. Whilst an expanded two‐tier analysis will address the issue of false positivity, it will not identify those IHC‐negative/FISH‐positive cases that we and others have found in a proportion of tumours (0.6–4.4%).10 Therefore, a frontline ISH test would be a more favourable option. Dual‐colour FISH is accepted as the gold standard for HER2 analysis; CISH has been shown here and previously5,11,12,13 to be as sensitive and specific. Other reports have shown a high but variable level of concordance (93.8–96%).3,6,14 The small number of discordant results in these reports have frequently been in the borderline samples due to the slight difference in cut‐off level between CISH and FISH.14 A HER2:CEP17 ratio of >2 is classed as amplified by FISH; however, with CISH (Zymed), a score of >5 HER2 signals is classed as amplified. A consensus should be reached on a clinically relevant cut‐off value for amplification for both ISH protocols.

Other FISH/CISH discrepancies have been due to inadequate use of chromosome 17 correction and difficult histology.3,6 By using chromosome 17 correction in all low amplified cases, light microscopy for assessment of HER2 in the histological context of the tumour sample and having experienced histopathologists analysing all the slides, we have not encountered these discrepancies between FISH and CISH results leading us to believe that CISH can reliably be used to assess breast tumour samples for patient eligibility for trastuzumab therapy.

Acknowledgements

We would like to thank Roche Products Ltd for the funding received for this study. The authors are independent of the funding organisation which sought no control over the design or content of the study.

Footnotes

Competing interests: none declared.

References

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