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Published Online First: 6 March 2008. doi:10.1136/jcp.2007.053850
Journal of Clinical Pathology 2008;61:757-760
Copyright © 2008 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.

ORIGINAL ARTICLES

A quality assurance exercise to evaluate the accuracy and reproducibility of chromogenic in situ hybridisation for HER2 analysis in breast cancer

S Di Palma1, N Collins2, M Bilous3, A Sapino4, M Mottolese5, N Kapranos6, F Schmitt7 and J Isola8

1 Department of Histopathology, Royal Surrey County Hospital and University of Surrey, Guildford, Surrey, UK
2 Department of Molecular Biology, Royal Surrey County Hospital, Guildford, Surrey, UK
3 Westmead Hospital, Sydney, New South Wales, Australia
4 Department of Biomedical Science and Human Oncology, University of Turin, Turin, Italy
5 Regina Elena Cancer Institute, Rome, Italy
6 MITERA Maternity and Surgical Center, Athens, Greece
7 IPATIMUP and Medical Faculty of Porto, Porto, Portugal
8 University of Tampere, Tampere, Finland

Correspondence to:
Silvana Di Palma, Department of Histopathology, Royal Surrey County Hospital, Guildford, Surrey, UK; silvana.dipalma{at}royalsurrey.nhs.uk

Background: Chromogenic in situ hybridisation (CISH) is an alternative to immunohistochemistry or FISH for the assessment of HER2 oncogene status in breast cancer. Although CISH is being used increasingly in routine diagnostics, there are no established inter-laboratory quality assurance programmes for this test.

Methods: The reproducibility of HER2 CISH analysis was assessed when performed by seven different centres that use the test routinely in diagnostic service.

Results: The results from 28 cases showed overall concordance of 98.5% (192/195 tests; {kappa} coefficient 0.91). One of the discrepancies was due to the invasive carcinoma having been cut out in the sections received by two of the centres, and the other two were in the non-amplified/equivocal/low-amplified category.

Conclusion: This is believed to be the first report of a quality assurance study assessing laboratories that use HER2 CISH routinely in clinical diagnostics. The results show that CISH is a robust technique providing a suitable assay for the frontline testing of HER2 status in breast cancer.


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This article has been cited by other articles:

  • Gong, Y., Sweet, W., Duh, Y.-J., Greenfield, L., Fang, Y., Zhao, J., Tarco, E., Symmans, W. F., Isola, J., Sneige, N. (2009). Chromogenic In Situ Hybridization Is a Reliable Method for Detecting HER2 Gene Status in Breast Cancer: A Multicenter Study Using Conventional Scoring Criteria and the New ASCO/CAP Recommendations. Am J Clin Pathol 131: 490-497 [Abstract] [Full Text]  

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