HercepTest: HER2 expression and gene amplification in non-small cell lung cancer

被引:81
作者
Cox, G
Vyberg, M
Melgaard, B
Askaa, J
Oster, A
O'Byrne, KJ
机构
[1] Leicester Royal Infirm, Dept Med Oncol, Leicester LE1 5WW, Leics, England
[2] Aalborg Univ Hosp, Inst Pathol, Aalborg, Denmark
[3] Dako, Glostrup, Denmark
关键词
HER2; HerceptTest; immunohistochemistry; prognosis; non-small-cell lung cancer;
D O I
10.1002/ijc.1214
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HER2 is an erbB/HER type I tyrosine kinase receptor that is frequently over-expressed in malignant epithelial tumours, Herceptin, a humanised mouse monoclonal antibody to HER2, is proven therapeutically in the management of metastatic breast cancer, significantly prolonging survival when combined with cytotoxic chemotherapeutic agents, Immunohistochemical studies suggest that non-small-cell lung cancer (NSCLC) tumours may over-express HER2, Our aim was to evaluate HER2 gene amplification and semi-quantitative immuno-expression in NSCLC. A total of 344 NSCLC cases were immunostained far HER2 expression in 2 centres using the HercepTest. Fluorescence in situ hybridisation (FISH) analysis for HER2 gene amplification was performed on most positive cases and a subset of negative cases. Fifteen cases (4.3%) demonstrated 2+ or 3+ membranous HER2 immuno-expression. There was no correlation between immuno-expression and tumour histology or grade. Tumours from higher-stage disease were more often HercepTest-positive (p < 0.001). All 4 HercepTest 3(+) cases demonstrated gene amplification, One of the 5 2+ cases tested for gene amplification showed areas of borderline amplification and areas of polyploidy. None of the 19 HercepTest-negative cases demonstrated gene amplification or polyploidy (p < 0.001). Gene amplification was demonstrated in all HercepTest 3+ scoring NSCLC cases. Unlike breast cancer, gene amplification and HER2 protein over-expression assessed by the HercepTest appeared to be uncommon in NSCLC. Herceptin may therefore target only a small proportion of NSCLC tumours and be of limited clinical value in this disease, particularly in the adjuvant setting, (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:480 / 483
页数:4
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