医学
免疫组织化学
内科学
胃肠病学
人口
人表皮生长因子受体2
胃食管交界处
癌症
胃
活检
病理
肿瘤科
乳腺癌
腺癌
环境卫生
作者
Woo Ho Kim,Lourdes Gómez Izquierdo,F Vilardell,Kent‐Man Chu,Geneviève Soucy,Lucas Vieira dos Santos,Geneviève Monges,Giuseppe Viale,María José Brito,Stuart Osborne,Johannes Noé,Xiang Du
出处
期刊:Applied Immunohistochemistry & Molecular Morphology
日期:2016-08-09
卷期号:26 (4): 239-245
被引量:40
标识
DOI:10.1097/pai.0000000000000423
摘要
Human epidermal growth factor receptor 2 (HER2) dysregulation is associated with tumorigenesis in gastric/gastroesophageal junction cancer; however, the number of patients with HER2-positive disease is unclear, possibly due to differing scoring criteria/assays. Data are also lacking for early disease. We aimed to assess the HER2-positivity rate using approved testing criteria in a large, real-life multinational population. HER2-positivity was defined as an immunohistochemistry staining score of 3+, or immunohistochemistry 2+ and HER2 amplification detected by in situ hybridization. A total of 4949 patients were enrolled and results showed that 14.2% of 4920 samples with immunohistochemistry results were HER2-positive. HER2-positivity was significantly higher in males (16.1% vs. 9.6% in females), in gastroesophageal versus stomach tumors (22.1% vs. 12.9%), in biopsy versus surgical samples (18.3% vs. 13.0%), in intestinal tumor subtypes versus diffuse (21.5% vs. 4.8%) and mixed types (21.5% vs. 8.5%) ( P <0.001), in mixed versus diffuse types (8.5% vs. 4.8%), and in “other” versus diffuse types (11.7% vs. 4.8%; P =0.002). There were no significant differences between stages. Patients in the youngest age percentile had significantly lower HER2-positivity rates than patients in the remaining percentiles (9.2% vs. 15.9%, 15.7%, and 15.1%; P <0.001). HER2-positivity was highest in France (20.2%) and lowest in Hong Kong (10.4%). In conclusion, HER-EAGLE, the first study of its kind to be conducted in a large, multinational population of almost 5000 patients, gives valuable insights into the real-world HER2-positivity rate in a gastric/gastroesophageal junction cancer patient population not selected for disease stage or histology.
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