c‐erbB‐2 Expression in small‐cell lung cancer is associated with poor prognosis

Small‐cell lung cancer (SCLC) carries a bad prognosis despite good initial response to chemotherapy. It is therefore important to identify molecular markers that influence survival as potential new therapeutic targets. In our study, expression of the tyrosine kinase c‐erbB‐2 (HER2/neu) receptor in t...

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Veröffentlicht in:International journal of cancer 2001-05, Vol.92 (4), p.474-479
Hauptverfasser: Micke, Patrick, Hengstler, Jan Georg, Ros, Roser, Bittinger, Fernando, Metz, Tsegay, Gebhard, Susanne, Beeh, Kai Michael, Oesch, Franz, Buhl, Roland
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container_end_page 479
container_issue 4
container_start_page 474
container_title International journal of cancer
container_volume 92
creator Micke, Patrick
Hengstler, Jan Georg
Ros, Roser
Bittinger, Fernando
Metz, Tsegay
Gebhard, Susanne
Beeh, Kai Michael
Oesch, Franz
Buhl, Roland
description Small‐cell lung cancer (SCLC) carries a bad prognosis despite good initial response to chemotherapy. It is therefore important to identify molecular markers that influence survival as potential new therapeutic targets. In our study, expression of the tyrosine kinase c‐erbB‐2 (HER2/neu) receptor in tumor tissues of 107 consecutive newly diagnosed patients with primary SCLC was quantified using a monoclonal antibody directed against the c‐terminal domain of c‐erbB‐2. A clear‐cut positive expression of c‐erbB‐2 was observed in 13% of patients. Surprisingly, c‐erbB‐2 was an independent prognostic factor (RR = 2.16; p = 0.014) when a proportional‐hazard model was adjusted to stage (limited vs. extensive disease) and performance status (WHO I–IV), the most relevant clinical parameters. Similarly, a significant association between c‐erbB‐2 and survival was obtained if a larger number of clinical parameters were included into the analysis, namely response to chemotherapy, TNM stage, lactate dehydrogenase (LDH), neuron‐specific enolase (NSE), gender and age (p = 0.033). Interestingly, c‐erbB‐2 expression was more relevant for patients with advanced tumors. In the subgroup of patients with bad performance status (WHO II–IV), median survival of patients with undetectable c‐erbB‐2 expression was 274 days compared with only 23 days for patients with clear‐cut positive c‐erbB‐2 immunohistochemistry (p = 0.0031; log‐rank test). Similar results were obtained for patients with extensive disease (p = 0.028) and high TNM stages (T>2 or N>1 or M1; p < 0.068, all comparisons). In contrast, c‐erbB‐2 expression was not associated with survival in patients with limited disease (p = 0.97), low TNM stages (p > 0.56, all comparisons) and good performance status (p = 0.97). In conclusion, c‐erbB‐2 is expressed in more than 10% of SCLC. Expression of c‐erbB‐2 is an independent prognostic factor of survival. The effect of c‐erbB‐2 expression seems to become more important in advanced stages of the disease. Since c‐erbB‐2 is a therapeutical target in other types of cancer, further studies to identify the role of c‐erbB‐2 in SCLC are clearly warranted. © 2001 Wiley‐Liss, Inc.
doi_str_mv 10.1002/ijc.1229
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It is therefore important to identify molecular markers that influence survival as potential new therapeutic targets. In our study, expression of the tyrosine kinase c‐erbB‐2 (HER2/neu) receptor in tumor tissues of 107 consecutive newly diagnosed patients with primary SCLC was quantified using a monoclonal antibody directed against the c‐terminal domain of c‐erbB‐2. A clear‐cut positive expression of c‐erbB‐2 was observed in 13% of patients. Surprisingly, c‐erbB‐2 was an independent prognostic factor (RR = 2.16; p = 0.014) when a proportional‐hazard model was adjusted to stage (limited vs. extensive disease) and performance status (WHO I–IV), the most relevant clinical parameters. Similarly, a significant association between c‐erbB‐2 and survival was obtained if a larger number of clinical parameters were included into the analysis, namely response to chemotherapy, TNM stage, lactate dehydrogenase (LDH), neuron‐specific enolase (NSE), gender and age (p = 0.033). Interestingly, c‐erbB‐2 expression was more relevant for patients with advanced tumors. In the subgroup of patients with bad performance status (WHO II–IV), median survival of patients with undetectable c‐erbB‐2 expression was 274 days compared with only 23 days for patients with clear‐cut positive c‐erbB‐2 immunohistochemistry (p = 0.0031; log‐rank test). Similar results were obtained for patients with extensive disease (p = 0.028) and high TNM stages (T&gt;2 or N&gt;1 or M1; p &lt; 0.068, all comparisons). In contrast, c‐erbB‐2 expression was not associated with survival in patients with limited disease (p = 0.97), low TNM stages (p &gt; 0.56, all comparisons) and good performance status (p = 0.97). In conclusion, c‐erbB‐2 is expressed in more than 10% of SCLC. Expression of c‐erbB‐2 is an independent prognostic factor of survival. The effect of c‐erbB‐2 expression seems to become more important in advanced stages of the disease. 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It is therefore important to identify molecular markers that influence survival as potential new therapeutic targets. In our study, expression of the tyrosine kinase c‐erbB‐2 (HER2/neu) receptor in tumor tissues of 107 consecutive newly diagnosed patients with primary SCLC was quantified using a monoclonal antibody directed against the c‐terminal domain of c‐erbB‐2. A clear‐cut positive expression of c‐erbB‐2 was observed in 13% of patients. Surprisingly, c‐erbB‐2 was an independent prognostic factor (RR = 2.16; p = 0.014) when a proportional‐hazard model was adjusted to stage (limited vs. extensive disease) and performance status (WHO I–IV), the most relevant clinical parameters. Similarly, a significant association between c‐erbB‐2 and survival was obtained if a larger number of clinical parameters were included into the analysis, namely response to chemotherapy, TNM stage, lactate dehydrogenase (LDH), neuron‐specific enolase (NSE), gender and age (p = 0.033). Interestingly, c‐erbB‐2 expression was more relevant for patients with advanced tumors. In the subgroup of patients with bad performance status (WHO II–IV), median survival of patients with undetectable c‐erbB‐2 expression was 274 days compared with only 23 days for patients with clear‐cut positive c‐erbB‐2 immunohistochemistry (p = 0.0031; log‐rank test). Similar results were obtained for patients with extensive disease (p = 0.028) and high TNM stages (T&gt;2 or N&gt;1 or M1; p &lt; 0.068, all comparisons). In contrast, c‐erbB‐2 expression was not associated with survival in patients with limited disease (p = 0.97), low TNM stages (p &gt; 0.56, all comparisons) and good performance status (p = 0.97). In conclusion, c‐erbB‐2 is expressed in more than 10% of SCLC. Expression of c‐erbB‐2 is an independent prognostic factor of survival. The effect of c‐erbB‐2 expression seems to become more important in advanced stages of the disease. 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It is therefore important to identify molecular markers that influence survival as potential new therapeutic targets. In our study, expression of the tyrosine kinase c‐erbB‐2 (HER2/neu) receptor in tumor tissues of 107 consecutive newly diagnosed patients with primary SCLC was quantified using a monoclonal antibody directed against the c‐terminal domain of c‐erbB‐2. A clear‐cut positive expression of c‐erbB‐2 was observed in 13% of patients. Surprisingly, c‐erbB‐2 was an independent prognostic factor (RR = 2.16; p = 0.014) when a proportional‐hazard model was adjusted to stage (limited vs. extensive disease) and performance status (WHO I–IV), the most relevant clinical parameters. Similarly, a significant association between c‐erbB‐2 and survival was obtained if a larger number of clinical parameters were included into the analysis, namely response to chemotherapy, TNM stage, lactate dehydrogenase (LDH), neuron‐specific enolase (NSE), gender and age (p = 0.033). Interestingly, c‐erbB‐2 expression was more relevant for patients with advanced tumors. In the subgroup of patients with bad performance status (WHO II–IV), median survival of patients with undetectable c‐erbB‐2 expression was 274 days compared with only 23 days for patients with clear‐cut positive c‐erbB‐2 immunohistochemistry (p = 0.0031; log‐rank test). Similar results were obtained for patients with extensive disease (p = 0.028) and high TNM stages (T&gt;2 or N&gt;1 or M1; p &lt; 0.068, all comparisons). In contrast, c‐erbB‐2 expression was not associated with survival in patients with limited disease (p = 0.97), low TNM stages (p &gt; 0.56, all comparisons) and good performance status (p = 0.97). In conclusion, c‐erbB‐2 is expressed in more than 10% of SCLC. Expression of c‐erbB‐2 is an independent prognostic factor of survival. The effect of c‐erbB‐2 expression seems to become more important in advanced stages of the disease. Since c‐erbB‐2 is a therapeutical target in other types of cancer, further studies to identify the role of c‐erbB‐2 in SCLC are clearly warranted. © 2001 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>11304679</pmid><doi>10.1002/ijc.1229</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Age Factors
Aged
Antibodies, Monoclonal - metabolism
Biological and medical sciences
c-erbB-2 gene
Carcinoma, Small Cell - diagnosis
Carcinoma, Small Cell - metabolism
Carcinoma, Small Cell - mortality
c‐erbB‐2
Disease-Free Survival
Female
HER‐2/neu
Humans
Immunohistochemistry
L-Lactate Dehydrogenase - biosynthesis
lung carcinoma
Lung Neoplasms - diagnosis
Lung Neoplasms - metabolism
Lung Neoplasms - mortality
Male
Medical sciences
Middle Aged
Phosphopyruvate Hydratase - biosynthesis
Pneumology
Prognosis
Proportional Hazards Models
Protein Structure, Tertiary
Receptor, ErbB-2 - biosynthesis
Sex Factors
small‐cell lung cancer
Time Factors
Treatment Outcome
Tumors of the respiratory system and mediastinum
title c‐erbB‐2 Expression in small‐cell lung cancer is associated with poor prognosis
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