Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/37045
Title: Comparing human epidermal growth factor receptor 2 amplification and expression using immunohistochemistry and silver in situ hybridisation in gastric carcinoma and lymph node metastasis
Authors: Gülten, G.
Yilmaz, B.
Demirkan, Neşe Çallı
Keywords: Gastric carcinoma
Human epidermal growth factor receptor 2
Microarray method
Silver in situ hybridisation
epidermal growth factor receptor 2
silver
trastuzumab
adult
Article
cancer grading
cancer staging
chromosome 17
diagnostic test accuracy study
distant metastasis
endoscopic biopsy
female
gastrectomy
gene amplification
gene expression
histopathology
human
human tissue
immunohistochemistry
in situ hybridization
lymph node dissection
lymph node metastasis
major clinical study
male
middle aged
predictive value
primary tumor
protein expression
scoring system
sensitivity and specificity
stomach adenocarcinoma
stomach carcinoma
tissue microarray
treatment planning
tumor volume
Publisher: Spandidos Publications
Abstract: Detecting the amplification and expression of human epidermal growth factor receptor (HER2) is important for planning trastuzumab treatment for patients with gastric carcinoma. The present study aimed to analyse HER2 amplification and expression in primary gastric adenocarcinoma tumours and metastatic lymph nodes using microarray methods, and to assess the potential contribution of these methods to treatment planning. In total, 60 patients with lymph node metastasis were included in the present study. Microarray blocks were obtained from the tissue blocks of primary tumours and metastatic lymph nodes. HER2 expression and amplification were investigated using immunohistochemical and silver in situ hybridisation (SISH) methods, respectively. Following immunohistochemical evaluation of HER2 in primary tumours, the sensitivity and specificity of the microarray method relative to the single block method were 69 and 100%, respectively. For HER2 detection in microarray block sections from primary tumours, the sensitivity and specificity of the SISH method relative to immunohistochemistry were 56 and 100%, respectively. When using SISH in microarray blocked sections, there was a high degree of concordance (98% concordance rate) between HER2 amplification in the primary tumour and the metastatic lymph node. Furthermore, the sensitivity and specificity of metastatic lymph node results relative to those of the primary tumour were 100 and 98%, respectively. Overall, the single block method was more reliable compared with the microarray method for planning treatment. When microarray blocking was used, a large number of samples must be tested to ensure reliable results. The immunohistochemical method is recommended as the first step as SISH alone increases the risk of false-negative results. Assessing HER2 amplification for treatment planning would be beneficial for primary tumours, as well as metastatic lymph nodes. © This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) License.
URI: https://hdl.handle.net/11499/37045
https://doi.org/10.3892/ol.2020.11731
ISSN: 1792-1074
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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