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Epidermal Growth Factor Receptor and HER2-neu mRNA Expression in Non-Small Cell Lung Cancer Is Correlated with Survival
The prognostic role of epidermal growth factor receptor (EGFR) and HER2-neu remains controversial in patients with non-small cell lung cancer (NSCLC). We studied the association between the mRNA expression of EGFR, HER2-neu, and survival in primary tumor and matching nonmalignant tissues from 83 pat...
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Published in: | Clinical cancer research 2001-07, Vol.7 (7), p.1850-1855 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The prognostic role of epidermal growth factor receptor (EGFR) and HER2-neu remains controversial in patients with non-small
cell lung cancer (NSCLC). We studied the association between the mRNA expression of EGFR, HER2-neu, and survival in primary
tumor and matching nonmalignant tissues from 83 patients with NSCLC. Analysis was performed using a quantitative real-time
PCR system (Taqman). EGFR and HER2-neu mRNA expression was detectable in all (100%) specimens analyzed. Twenty-nine (34.9%)
patients had high HER2-neu expression, and 28 (33.7%) patients had high EGFR expression. A high HER2-neu and EGFR coexpression
was detectable in 14 (16.9%) patients. High HER2-neu expression was associated with inferior survival ( P = 0.004), whereas high EGFR expression showed a trend toward inferior survival ( P = 0.176). The impact of HER2-neu and EGFR coexpression on patients’ survival was additive ( P = 0.003). Multivariate analysis determined high HER2-neu expression ( P = 0.041), and high EGFR/HER2-neu coexpression ( P = 0.030) as significant and independent unfavorable prognostic factors. These findings indicate that HER2-neu and EGFR play
a crucial role in the biological behavior of NSCLCs. Testing of molecular marker coexpression (EGFR and HER2-neu) improves
the estimation of prognosis and appears to define low- and high-risk groups for treatment failure in curatively resected NSCLC. |
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ISSN: | 1078-0432 1557-3265 |