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Published Online First: 26 January 2007. doi:10.1136/jcp.2006.044701
Journal of Clinical Pathology 2007;60:1277-1283
Copyright © 2007 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.

ORIGINAL ARTICLES

Frequency and reliability of oestrogen receptor, progesterone receptor and HER2 in breast carcinoma determined by immunohistochemistry in Australasia: results of the RCPA Quality Assurance Program

Glenn D Francis1, Margaret Dimech2, Leanne Giles2 and Alison Hopkins2

1 Queensland Health Pathology Service, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia
2 RCPA Quality Assurance Programs Pty Ltd, Anatomical Pathology, Burwood, Victoria, Australia

Correspondence to:
Dr Glenn D Francis, Queensland Health Pathology Service, Princess Alexandra Hospital, Ipswich Rd, Woolloongabba, Queensland, Australia 4102; Glenn_Francis{at}health.qld.gov.au

Background and Aims: Immunohistochemistry (IHC) has replaced radioligand binding assay for the determination of oestrogen receptor (ER) status in breast carcinoma. IHC is also used for assessment of progesterone receptor (PR) and HER2. The Royal College of Pathologists of Australasia (RCPA) Quality Assurance Program (QAP) introduced a breast markers module in 2003 to evaluate the performance of laboratories with IHC for ER, PR and HER2.

Methods: An audit of laboratories reporting breast carcinomas was performed in 2005 and 2006 to evaluate in-house results. Laboratories were asked to submit the hormone receptor and HER2 status on each invasive breast carcinoma for the previous 6 month period up to a maximum of 100 cases. The time periods were 1 July 2004 to 31 December 2004, and 1 July 2005 to 31 December 2005. A total of 55 laboratories returned information for 2004 and 67 for 2005.

Results: Complete data on 8128 patients was returned for both surveys, 3353 cases for 2004 and 4775 for 2005. The results were similar for both surveys. Of the 8128 cases, 59.0% were ER+/PR+, 15.9% ER+/PR–, 2.4% ER–/PR+ and 22.7% ER–/PR–. HER2 data were submitted for a total of 6512 patients (excludes 52 patients with incomplete data sets); 17.1% were reported as 3+ positive on IHC, 12.5% as 2+ and 70.4% as negative.

Conclusions: A laboratory audit was introduced into the RCPA QAP for breast markers due to concerns raised by participating laboratories about technical differences in supplied tissues for testing. This audit indicates that overall the results for ER, PR and HER2 fall inside established parameters. However, a number of individual laboratories do not meet the target values and variation in results would impact on patient treatment decisions.

Abbreviations: ER, oestrogen receptor; FISH, fluorescence in-situ hybridisation; HR, hormone receptor; IHC, immunohistochemistry; ISH, in-situ hybridisation; PR, progesterone receptor; QAP, Quality Assurance Program; RCPA, Royal college of Pathologists of Australasia


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