Literature DB >> 28823752

HER2 testing in advanced gastric and gastro-oesophageal cancer: analysis of an Australia-wide testing program.

M Priyanthi Kumarasinghe1, Adrienne Morey2, Michael Bilous3, Gelareh Farshid4, Glenn Francis5, Guy Lampe6, Glenda McCue7, Vita Von Neumann-Cosel8, Stephen B Fox9.   

Abstract

This Australian human epidermal growth factor receptor 2 (HER2) testing program aimed to analyse >800 cases tested in a coordinated setting to further evaluate the criteria to establish HER2 status in advanced gastric and gastro-oesophageal junction (GOJ) cancer. Heterogeneity, and minimum number of biopsy fragments for reliable HER2 assessment were also examined in a subset of samples. Five laboratories tested 891 samples referred to determine HER2 status for potential anti-HER2 treatment. Cancer site, specimen type (endoscopic biopsy/resection/metastases), immunohistochemistry (IHC) score, HER2 gene and CEP17 copy number (CN) and HER2:CEP17 ratios were recorded. Samples were derived from stomach (53.1%), GOJ (28.2%) or metastases (18.5%). IHC for HER2 and dual probe HER2:CEP17 in situ hybridisation (ISH) were performed in parallel. A stringent definition (SD) of HER2 positivity was used (IHC2+/3+ plus CN>6 and ratio>2) and compared with other published criteria. HER2 positive rate was 13.9% (114/820) by SD, and 12.9-16.0% using other definitions. There was higher concordance between IHC and HER2 CN by ISH than with ratio. The HER2 positive rate was significantly higher in GOJ samples than others (p = 0.03) and in endoscopic biopsies than resections (p = 0.047). In a subset of 98 positive cases, 39 (39.8%) showed heterogeneity, and in 282 endoscopic biopsies positivity rate plateaued at five tumour fragments, suggesting this is the minimum number of biopsies that should be examined.
Copyright © 2017 Royal College of Pathologists of Australasia. All rights reserved.

Entities:  

Keywords:  Gastric cancer; gastro-oesophageal cancer; human epidermal growth factor receptor 2 (HER2); immunohistochemistry; in situ hybridisation

Mesh:

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Year:  2017        PMID: 28823752     DOI: 10.1016/j.pathol.2017.05.009

Source DB:  PubMed          Journal:  Pathology        ISSN: 0031-3025            Impact factor:   5.306


  2 in total

1.  Identification of the hub genes RUNX2 and FN1 in gastric cancer.

Authors:  Chao Han; Lei Jin; Xuemei Ma; Qin Hao; Huajun Lin; Zhongtao Zhang
Journal:  Open Med (Wars)       Date:  2020-05-30

2.  A Pilot Study of Baseline Spatial Genomic Heterogeneity in Primary Gastric Cancers Using Multi-Region Endoscopic Sampling.

Authors:  Joseph Chao; Jeeyun Lee; Kyung Kim; So Young Kang; Taehyang Lee; Kyoung-Mee Kim; Seung Tae Kim; Samuel J Klempner; Hyuk Lee
Journal:  Front Oncol       Date:  2020-02-25       Impact factor: 6.244

  2 in total

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