Volume 199, Issue 4 p. 418-423
Original Paper

Correlation between immunohistochemistry (HercepTest) and fluorescence in situ hybridization (FISH) for HER-2 in 426 breast carcinomas from 37 centres

M Dowsett

Corresponding Author

M Dowsett

Academic Department of Biochemistry, Royal Marsden NHS Trust, London, UK

Academic Department of Biochemistry, Royal Marsden NHS Trust, Fulham Road, London SW3 6JJ, UK.Search for more papers by this author
J Bartlett

J Bartlett

University Department of Surgery, Glasgow Royal Infirmary, Glasgow, UK

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IO Ellis

IO Ellis

Department of Pathology, Nottingham City Hospital, Nottingham, UK

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J Salter

J Salter

Academic Department of Biochemistry, Royal Marsden NHS Trust, London, UK

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M Hills

M Hills

Academic Department of Biochemistry, Royal Marsden NHS Trust, London, UK

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E Mallon

E Mallon

University Department of Pathology, Western Infirmary, Glasgow, UK

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AD Watters

AD Watters

University Department of Surgery, Glasgow Royal Infirmary, Glasgow, UK

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T Cooke

T Cooke

University Department of Surgery, Glasgow Royal Infirmary, Glasgow, UK

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C Paish

C Paish

Department of Pathology, Nottingham City Hospital, Nottingham, UK

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PM Wencyk

PM Wencyk

Department of Pathology, Nottingham City Hospital, Nottingham, UK

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SE Pinder

SE Pinder

Department of Pathology, Nottingham City Hospital, Nottingham, UK

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First published: 07 February 2003
Citations: 186

Abstract

Accurate diagnostic assessment of HER-2 is essential for the appropriate application of the humanized anti-HER-2 monoclonal antibody trastuzumab (Herceptin) to the treatment of patients with metastatic breast cancer. The diagnostic test needs to be applicable to archival, fixed tissue removed at excision, in many cases several years earlier. We compared the assessment of HER-2 by immunohistochemistry (IHC; HercepTest) and fluorescence in situ hybridization (FISH) in 426 breast carcinomas from patients being considered for trastuzumab therapy. The tumours were tested in three reference centres having been sent in from 37 hospitals. Only 2/270 (0.7%) IHC 0/1+ tumours were FISH positive. Six of 102 (5.9%) IHC 3+ tumours were FISH negative. Five of the six had between 1.75 and 2.0 HER-2 gene copies per chromosome 17 and the sixth had multiple copies of chromosome 17. Thirteen per cent of tumours were IHC 2+ and overall 48% of these were FISH positive but this proportion varied markedly between the centres. Sixty IHC-stained slides selected to be enriched with 2+ cases were circulated between the three laboratories and scored. There were 20 cases in which there was some discordance in scoring. Consideration of the FISH score in these cases led to concordance in the designation of positivity/negativity in 19 of these 20 cases. These data support an algorithm in which FISH testing is restricted to IHC 2+ tumours in reference centres. The results may not extrapolate to laboratories with less experience or using different methodologies. Copyright © 2003 John Wiley & Sons, Ltd.