Volume 64, Issue 5 pp. 633-638
Original Article

Epidermal growth factor receptor (EGFR), HER2 and insulin-like growth factor-1 receptor (IGF-1R) status in ovarian adult granulosa cell tumours

Patricia A Higgins

Patricia A Higgins

Northern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queens University Belfast, Belfast Health and Social Care Trust, Belfast, UK

Department of Pathology, Belfast Health and Social Care Trust, Belfast, UK

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Aidan Brady

Aidan Brady

Department of Pathology, Belfast Health and Social Care Trust, Belfast, UK

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Stephen P Dobbs

Stephen P Dobbs

Department of Gynaecological Oncology, Belfast Health and Social Care Trust, Belfast, UK

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Manuel Salto-Tellez

Manuel Salto-Tellez

Northern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queens University Belfast, Belfast Health and Social Care Trust, Belfast, UK

Department of Pathology, Belfast Health and Social Care Trust, Belfast, UK

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Perry Maxwell

Perry Maxwell

Northern Ireland Molecular Pathology Laboratory, Centre for Cancer Research and Cell Biology, Queens University Belfast, Belfast Health and Social Care Trust, Belfast, UK

Department of Pathology, Belfast Health and Social Care Trust, Belfast, UK

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W Glenn McCluggage

Corresponding Author

W Glenn McCluggage

Department of Pathology, Belfast Health and Social Care Trust, Belfast, UK

Address for correspondence: W G McCluggage, Department of Pathology, Royal Group of Hospitals Trust, Grosvenor Road, Belfast BT12 6BA, Northern Ireland, UK. e-mail: [email protected]Search for more papers by this author
First published: 07 November 2013
Citations: 11

Abstract

Aims

Adult granulosa cell tumours (AGCTs) are uncommon ovarian sex cord–stromal tumours which recur following surgical removal in up to 50% of patients. Treatment options for recurrent and advanced stage AGCTs are limited, with poor response to chemotherapy and radiotherapy. We aimed to assess epidermal growth factor receptor (EGFR), HER2 and insulin-like growth factor-1 receptor (IGF-1R) status in AGCTs with a view to investigating whether or not these receptors might be potential therapeutic targets in these neoplasms.

Methods and results

Immunohistochemical staining for EGFR, HER2 and IGF-1R was undertaken in 31 AGCTs. Tumour DNA was also analysed for mutations in the tyrosine kinase domain of EGFR (exons 18–21) by Cobas mutation RT–PCR. Twenty-three of 31 (74%) AGCTs showed some degree of EGFR expression, generally with cytoplasmic or mixed membranous and cytoplasmic staining of variable intensity. Eleven of 27 (41%) cases exhibited strong membranous and cytoplasmic expression of IGF-1R. HER2 expression was not seen. No mutations were found in exons 18–21 of the EGFR gene in hot-spots of therapeutic relevance.

Conclusions

This study raises the possibility that anti-EGFR and/or anti-IGF-1R therapies may be of potential benefit in ovarian AGCTs, and this requires further study. Lack of known mutations within the tyrosine kinase domain of EGFR suggests that EGFR-related tyrosine kinase inhibitors may not be useful therapeutically.

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