HER2 in Gastric Cancer: ESMO Biomarker Factsheet

Giuseppe Viale
Giuseppe Viale
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Giuseppe Viale
University of Milan, European Institute of Oncology, Milan, Italy

Definition of HER2

Human Epidermal growth factor 2 (HER2, ERBB2) is a membrane-associated receptor that dimerises with HER family members and transduces extracellular signals to RAS-MAP kinase and PI3 kinase-Akt intracellular signalling networks. HER2 is overexpressed in several types of tumours, including gastro-oesophageal adenocarcinoma.

In gastric cancer, HER2 acts as an oncogene. Protein overexpression is associated with genetic Amplification of segments of chromosome 17 that may form tandem duplications on chromosome 17 or double-minute Chromosomes.

HER2 Overexpression in Gastric Cancer

HER2 is overexpressed in about 30% of intestinal type gastric cancers, 15% of mixed type tumours, and about 5% of diffuse type. Signet ring type is typically HER2 negative. According to tumour location, about 30% of tumours at cardiac/gastro–oesophageal junction and 15% of gastric cancers show HER2 positivity.

HER2 as a Prognostic Biomarker in Gastric Cancer

There is mounting evidence of the role of HER2 overexpression in patients with gastric cancer, and it has been correlated to poor outcomes and a more aggressive disease. Many investigations have been conducted on HER2 as a Prognostic factor; although there have been no universal conclusions, the positive result of HER2 status appears to be poor prognostic factor. All the studies have encountered problems such as small sample size, diversity of patient characteristics, methods of HER2 tests and diagnosis of HER2 status. HER2 status seems not to be an independent prognostic Biomarker in early oesophago-gastric adenocarcinoma.

HER2 as a Predictive Biomarker in Gastric Cancer

Clinically, HER2 has been established as a predictive biomarker for HER2-targeted therapies. In gastric cancer, it is a predictive biomarker for treatment with trastuzumab. Since trastuzumab, in combination with chemotherapy, significantly improves survival for patients with advanced HER2-positive gastric and gastro-esophageal junction adenocarcinoma over chemotherapy alone, the combination therapy became the standard of care in HER2-positive advanced disease. Therefore, appropriate patient selection by HER2 Immunohistochemistry and in situ hybridization should be part of routine pathology.

HER2 Testing Recommendations in Gastric Cancer

Intense membranous immunoreactivity for HER2 in almost all the tumour cells of a gastric adenocarcinoma

Intense membranous immunoreactivity for HER2 in almost all the tumour cells of a gastric adenocarcinoma
Credit: Giuseppe Viale

Representative surgical samples or an adequate number of viable biopsy specimens (ideally six to eight) are required. If few biopsies are available, all viable specimens should be tested. Immunohistochemistry should be the initial HER2 testing methodology for gastric cancer and bright-field methodologies are preferred wherever possible.

HER2-positivity per European Medicines Agency license is defined as immunohistochemistry 3+ or immunohistochemistry 2+/fluorescence in situ hybridization-positive or immunohistochemistry 2+/silver in situ hybridization-positive.

Tumour samples classified as immunohistochemistry 2+ should be retested by fluorescence in situ hybridization or silver in situ hybridization to assess HER2 status.

Silver in situ hybridization is a more suitable methodology than fluorescence in situ hybridization for assessing HER2 status in gastric tumour samples as it is a bright-field methodology and thus allows for rapid identification of HER2-positive tumour foci within a heterogeneous sample.

Scoring Recommendations


Small biopsy sample of gastric adenocarcinoma, showing a single small focus of immunoreactive tumour cells

Small biopsy sample of gastric adenocarcinoma, showing a single small focus of immunoreactive tumour cells
Credit: Giuseppe Viale

These criteria were modified from breast cancer criteria to account for common, idiosyncratic staining characteristics of gastro-oesophageal cancers (eg. basolateral HER2 localisation and heterogeneous staining). Due to the tumour heterogeneity (focal areas of positivity) and incomplete membrane staining, the gastric cancer-specific scoring criteria should be adhered to:

  • Surgical specimen cutoff: complete, basolateral, or lateral membranous reactivity in ≥10% of cells
  • Biopsy specimen cutoff: complete, basolateral, or lateral membranous reactivity in ≥5 clustered cells

The ‘magnification rule’ should be used in conjunction with the scoring criteria.

In situ hybridization

Fluorescence in situ hybridization showing a nest of tumour cells with HER2 gene amplification (red signals)

Fluorescence in situ hybridization showing a nest of tumour cells with HER2 Gene amplification (red signals)
Credit: Giuseppe Viale

The definition of fluorescence in situ hybridization or silver in situ hybridization positivity in gastric or gastro–oesophageal junction cancer is a HER2: chromosome 17 ratio of ≥2.0. The entire section should be screened for amplified regions (particularly important for fluorescence in situ hybridization samples where a bright-field image is not available). At least 20 evaluable, non-overlapping cells in the invasive component should be counted initially. In borderline amplification cases, approximately 20 additional cells should be recounted or scoring should be performed in an alternative area of tissue. The overall HER2 Gene count is important: >6 HER2 gene copies using single probe is considered positive; in case of 4 to 6 HER2 gene copies a dual probe test is advised and the ratio should be recalculated by counting an additional 20 cells.

Ensuring Quality and Timely HER2 Testing Results

Validated immunohistochemistry and in situ hybridization HER2 assays should be used and appropriate controls should be included in each run. Turnaround time from initial diagnosis to reporting of results should ideally not exceed 5 working days. Centralised testing is recommended wherever possible and all laboratories should be encouraged to participate in validated quality assurance programs.

Which Technique and Which Algorithm Should be Used for the Analysis of the HER2 Status in Gastric Cancer?

Immunohistochemically based HER2 screening algorithm is a pragmatic strategy used by many laboratories owing to the relative labour-intensiveness of in situ hybridization, even though trastuzumab therapy is approved for all patients with ISH-positive gastro-oesophageal cancers (regardless of immunohistochemical score) in the United States. An immunohistochemistry-first screening protocol demands high concordance of the immunohistochemical and ISH assays. The optimal immunohistochemical screening assay should also demonstrate high sensitivity and low false-negative rates for ISH amplification to ensure that all patients who may benefit from anti-HER2 therapy are identified.

Patient Selection

In Europe, immunohistochemistry is recommended as the first testing modality and in situ hybridization technique should be applied only in cases of immunohistochemistry 2+. Immunohistochemistry 0 and 1+ are not eligible for trastuzumab therapy. Borderline immunohistochemistry 1+/immunohistochemistry 2+ cases and samples with focal and intense membranous reactivity in <10% cells may be retested with fluorescence in situ hybridization or silver in situ hybridization (scores for both assays should be indicated separately on the report).


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Last update: 03 August 2015