HER2 Human Epidermal growth factor Receptor 2 Excess HER2 gene leads to over expression of HER2 protein 20-30% Of breast cancers over express HER2.

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HER2 Human Epidermal growth factor Receptor 2 Excess HER2 gene leads to over expression of HER2 protein 20-30% Of breast cancers over express HER2

Her2 and breast cancer  Prognostic marker: Poor clinical outcomes  Predictive marker: Response to Transtuzumab [Herceptin] Tamoxifen resistance Anthracyclines

Which patients?  All patients with metastases.  All newly diagnosed patients.

How? Immunocytochemistry: antibody to HER2 protein [gene product] 0/1+Negative 2+Equivocal 3+Positive

In Situ Hybridisation [ISH] F.I.S.H. [Fluorescent ISH] quantifies the gene amplification

Herceptin in early breast cancer  ASCO 2005 HERA and NSABP B-31 October 2005 DoH SEHD

WoSCAN  Testing: All newly diagnosed patients All metastatic cases  I.H.C Ayrshire and Arran [2002] Glasgow [2004] {Lanarkshire, Argyll and Clyde, Forth Valley.} Dumfries and Galloway  FISH Glasgow

SCAN  Testing All metastatic cases All “ high risk” new diagnoses  IHC & FISH Edinburgh {Lothian, Fife and the Borders}

NoSCAN  Grampian Testing: All newly diagnosed cases All metastatic cases  Aberdeen IHC Pathology FISH Cytogenetics

 Inverness Testing: Metastatic cases only  IHC & FISH Pathlore

 Tayside Testing: All new cases All metastatic cases  Dundee IHCPathology FISHCytogenetics

Strengths  Substantial numbers of new patients already tested.  NEQAS participation  Innovative approach  Utilising regional MCNs

Challenges  Not all new patients being tested  Backlog  Funding  Quality assurance  Turnaround times  Numbers  IHC which antibody?

HER2 Service  All pertinent patients  Quality Assurance Standards  Results available in clinically relevant timescales.

Molecular Diagnostics  Comprehensive  Infrastructure  Versatile