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

被引:8
作者
Kumarasinghe, M. Priyanthi [1 ,2 ]
Morey, Adrienne [3 ]
Bilous, Michael [4 ]
Farshid, Gelareh [5 ,6 ]
Francis, Glenn [7 ]
Lampe, Guy [8 ]
McCue, Glenda [9 ]
Von Neumann-Cosel, Vita [10 ]
Fox, Stephen B. [11 ,12 ]
机构
[1] Univ Western Australia, QEII Med Ctr, PathWest, Perth, WA, Australia
[2] Univ Western Australia, Sch Pathol & Lab Med, Perth, WA, Australia
[3] St Vincents Hosp, SydPath, Sydney, NSW, Australia
[4] Norwest Private Hosp, Australian Clin Labs, Bella Vista, NSW, Australia
[5] Univ Adelaide, Discipline Med, Adelaide, SA, Australia
[6] SA Pathol, Directorate Surg Pathol, Adelaide, SA, Australia
[7] Genom Life, Brisbane, Qld, Australia
[8] Pathol Queensland, Brisbane, Qld, Australia
[9] Woolomin Consulting, Wheeo, NSW, Australia
[10] Roche Prod Pty Ltd, Dee Why, NSW, Australia
[11] Univ Melbourne, Peter MacCallum Canc Ctr, Melbourne, Vic, Australia
[12] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic, Australia
关键词
Gastric cancer; gastro-oesophageal cancer; human epidermal growth factor receptor 2 (HER2); immunohistochemistry; in situ hybridisation; GROWTH-FACTOR RECEPTOR; GENE AMPLIFICATION; METASTATIC SITES; CARCINOMA; MUTATIONS; CONCORDANCE; VALIDATION; EXPRESSION; GUIDELINE; SURVIVAL;
D O I
10.1016/j.pathol.2017.05.009
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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/metas-tases), 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.
引用
收藏
页码:575 / 581
页数:7
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