Characterisation and predictive value of epidermal growth factor receptor status using quantitative real-time PCR combined with immunohistochemistry on non-small cell lung cancer specimens

被引:0
作者
Hilbe, W
Dlaska, M
Dirnhofer, S
Duba, HC
Eisterer, W
Oberwasserlechner, F
Mildner, A
Schmid, T
Ammann, K
Thaler, J
Wöll, E
机构
[1] Univ Innsbruck Hosp, Dept Internal Med, A-6020 Innsbruck, Austria
[2] Univ Basel, Dept Pathol, CH-4003 Basel, Switzerland
[3] Univ Innsbruck, Dept Med Biol & Human Genet, A-6020 Innsbruck, Austria
[4] Univ Innsbruck Hosp, Dept Surg, A-6020 Innsbruck, Austria
[5] Natters State Hosp, Dept Surg, Innsbruck, Austria
[6] Gen Hosp, Dept Oncol Hematol & Immunol, Wels, Austria
关键词
quantitative real-time PCR; EGFR; lung cancer; immunohistochemistry;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The frequency of increased EGFR-mRNA expression was determined in 57 patients suffering from NSCLC by applying quantitative real-time PCR. The findings were correlated with clinical parameters and the immunohistochemical (IHC) markers EGFR, c-erbB-2, c-erbB-3, Ki-67 and p53 on cryostat sections. Of the patients 46% showed increased EGFR-mRNA, 35% revealed an increased IHC-EGFR expression; 16% of the patients showed a combined positivity and 35% a combined negativity when applying both methods, and 17 (30%) of the cases revealed increased EGFR-mRNA without IHC-EGFR expression. This subgroup was characterised by p53 coexpression and the highest frequency of deaths (35% vs. 20%) indicating a more aggressive tumour type. In contrast to IHC - where positivity was seen predominantly in squamous cell carcinomas (48% vs. 27%) - EGFR-mRNA expression was observed equally in both histological subtypes (48% vs. 43%). PCR-EGFR and IHC-EGFR tumour typing identifies different tumour characteristics with different clinical courses. Whether this combined typing could help to identify patients who respond to anti-EGFR therapies is worth further testing.
引用
收藏
页码:893 / 899
页数:7
相关论文
共 38 条
[1]  
Bièche I, 1999, CLIN CHEM, V45, P1148
[2]  
Brabender J, 2001, CLIN CANCER RES, V7, P1850
[3]   The new World Health Organization classification of lung tumours [J].
Brambilla, E ;
Travis, WD ;
Colby, TV ;
Corrin, B ;
Shimosato, Y .
EUROPEAN RESPIRATORY JOURNAL, 2001, 18 (06) :1059-1068
[4]  
BUNN PA, 2002, NOVEL TARGETED AGENT, P683
[5]   HercepTest: HER2 expression and gene amplification in non-small cell lung cancer [J].
Cox, G ;
Vyberg, M ;
Melgaard, B ;
Askaa, J ;
Oster, A ;
O'Byrne, KJ .
INTERNATIONAL JOURNAL OF CANCER, 2001, 92 (04) :480-483
[6]   Molecular biologic substaging of stage I lung cancer according to gender and histology [J].
D'Amico, TA ;
Aloia, TA ;
Moor, MBH ;
Herndon, JE ;
Brooks, KR ;
Lau, CL ;
Harpole, DH .
ANNALS OF THORACIC SURGERY, 2000, 69 (03) :882-886
[7]  
DARMSTRUP L, 2002, INT J CANCER, V97, P7
[8]   EPIDERMAL GROWTH-FACTOR RECEPTOR IN LUNG MALIGNANCIES - COMPARISON BETWEEN CANCER AND NORMAL TISSUE [J].
DITTADI, R ;
GION, M ;
PAGAN, V ;
BRAZZALE, A ;
DELMASCHIO, O ;
BARGOSSI, A ;
BUSETTO, A ;
BRUSCAGNIN, G .
BRITISH JOURNAL OF CANCER, 1991, 64 (04) :741-744
[9]   Novel targets for lung cancer therapy: Part I [J].
Dy, GK ;
Adjei, AA .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (12) :2881-2894
[10]   EPIDERMAL GROWTH-FACTOR RECEPTOR (EGFR) EXPRESSION IN NONSMALL CELL LUNG CARCINOMAS CORRELATES WITH METASTATIC INVOLVEMENT OF HILAR AND MEDIASTINAL LYMPH-NODES IN THE SQUAMOUS SUBTYPE [J].
FONTANINI, G ;
VIGNATI, S ;
BIGINI, D ;
MUSSI, A ;
LUCCHI, H ;
ANGELETTI, CA ;
PINGITORE, R ;
PEPE, S ;
BASOLO, F ;
BEVILACQUA, G .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (02) :178-183