HER2 Support Group Forums - View Single Post - Correction for chromosome-17 is critical for the accurate Her-2/neu status

heblaj01 · 10-18-2006, 06:41 PM

Does anyone know which procedure is commonly used by labs to diagnostic HER2 status? Is it the procedure recommanded in this article which looked at the one that demonstrates the best concordant results between the FISH, IHC & BASNA methods?

http://mct.aacrjournals.org/cgi/cont...ract/5/10/2572

Correction for chromosome-17 is critical for the determination of true Her-2/neu gene amplification status in breast cancer

Abstract Purpose: Trastuzumab is the cornerstone for treatment of women with HER2-overexpressing breast cancer, both in the adjuvant and in the metastatic settings. The accurate assessment of HER2 is, therefore, critical to identifying patients who may benefit from trastuzumab-based therapy. This project aimed to determine the optimal scoring method for fluorescence in situ hybridization (FISH) assay.
Methods: FISH assay was done on 893 samples of breast cancer. Three scoring methods were evaluated: Her2/CEP17

2, Her2>4, or Her2>6. Protein and gene expression were evaluated by immunohistochemistry (n = 584) and mRNA/assay/nucleic acid sequence–based amplification (NASBA; n = 90). Results: Samples were divided into five groups based on FISH results: disomic amplified and nonamplified, polysomic amplified, nonamplified, and discordant (10.8% of cases, mostly positive with Her2>4 scoring, but negative with the others). Her2/CEP17

2 and Her2>6 scoring methods showed the best association (a) with regard to FISH scoring (k= 0.906, P < 10–6) and (b) between FISH and immunohistochemistry (3+ as positive; k> 0.650, P < 10–6) or NASBA (k> 0.536, P < 10–6). Polysomy had an effect on Her2 copy number (P < 10–6), but had no effect on protein and mRNA content. Therefore, within the discordant subgroup, for which additive Her-2 gene copies are due to high polysomy, protein and mRNA levels were similar to those of the nonamplified samples. For this subgroup, the best concordance between FISH/immunohistochemistry/NASBA was observed with the Her2/CEP17 ratio and Her-2>6 scoring (68% and 58% perfect matches, respectively). No perfect matches were observed using the Her2>4 scoring method. Conclusion: Correction for chromosome-17 is the method of choice for clinical practice; Her-2>6, but not Her-2>4, could be used as an alternative. [Mol Cancer Ther 2006;5(10):2572–9]

10-18-2006, 06:41 PM	#1
heblaj01 Senior Member Join Date: Apr 2006 Posts: 543	Correction for chromosome-17 is critical for the accurate Her-2/neu status Does anyone know which procedure is commonly used by labs to diagnostic HER2 status? Is it the procedure recommanded in this article which looked at the one that demonstrates the best concordant results between the FISH, IHC & BASNA methods? http://mct.aacrjournals.org/cgi/cont...ract/5/10/2572 *Correction for chromosome-17 is critical for the determination of true Her-2/neu* gene amplification status in breast cancer Abstract Purpose:** Trastuzumab is the cornerstone for treatment of women with HER2-overexpressing breast cancer, both in the adjuvant and in the metastatic settings. The accurate assessment of HER2 is, therefore, critical to identifying patients who may benefit from trastuzumab-based therapy. This project aimed to determine the optimal scoring method for fluorescence in situ hybridization (FISH) assay. *Methods:* FISH assay was done on 893 samples of breast cancer. Three scoring methods were evaluated: Her2/CEP172, Her2>4, or Her2>6. Protein and gene expression were evaluated by immunohistochemistry (n = 584) and mRNA/assay/nucleic acid sequence–based amplification (NASBA; n = 90). *Results:* Samples were divided into five groups based on FISH results: disomic amplified and nonamplified, polysomic amplified, nonamplified, and discordant (10.8% of cases, mostly positive with Her2>4 scoring, but negative with the others). Her2/CEP172 and Her2>6 scoring methods showed the best association (a) with regard to FISH scoring (k= 0.906, P < 10–6) and (b) between FISH and immunohistochemistry (3+ as positive; k> 0.650, P < 10–6) or NASBA (k> 0.536, P < 10–6). Polysomy had an effect on Her2 copy number (P < 10–6), but had no effect on protein and mRNA content. Therefore, within the discordant subgroup, for which additive Her-2 gene copies are due to high polysomy, protein and mRNA levels were similar to those of the nonamplified samples. For this subgroup, the best concordance between FISH/immunohistochemistry/NASBA was observed with the Her2/CEP17 ratio and Her-2>6 scoring (68% and 58% perfect matches, respectively). No perfect matches were observed using the Her2>4 scoring method. *Conclusion:* Correction for chromosome-17 is the method of choice for clinical practice; Her-2>6, but not Her-2>4, could be used as an alternative. [Mol Cancer Ther 2006;5(10):2572–9]