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 |
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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>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.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.1229</identifier><identifier>PMID: 11304679</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>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</subject><ispartof>International journal of cancer, 2001-05, Vol.92 (4), p.474-479</ispartof><rights>Copyright © 2001 Wiley‐Liss, Inc.</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4119-9c2cb74793ed89db91eedcc9431f4416e24403e7b8f1e8213c3fbb5012a64e923</citedby><cites>FETCH-LOGICAL-c4119-9c2cb74793ed89db91eedcc9431f4416e24403e7b8f1e8213c3fbb5012a64e923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.1229$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.1229$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1087135$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11304679$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Micke, Patrick</creatorcontrib><creatorcontrib>Hengstler, Jan Georg</creatorcontrib><creatorcontrib>Ros, Roser</creatorcontrib><creatorcontrib>Bittinger, Fernando</creatorcontrib><creatorcontrib>Metz, Tsegay</creatorcontrib><creatorcontrib>Gebhard, Susanne</creatorcontrib><creatorcontrib>Beeh, Kai Michael</creatorcontrib><creatorcontrib>Oesch, Franz</creatorcontrib><creatorcontrib>Buhl, Roland</creatorcontrib><title>c‐erbB‐2 Expression in small‐cell lung cancer is associated with poor prognosis</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><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.</description><subject>Age Factors</subject><subject>Aged</subject><subject>Antibodies, Monoclonal - metabolism</subject><subject>Biological and medical sciences</subject><subject>c-erbB-2 gene</subject><subject>Carcinoma, Small Cell - diagnosis</subject><subject>Carcinoma, Small Cell - metabolism</subject><subject>Carcinoma, Small Cell - mortality</subject><subject>c‐erbB‐2</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>HER‐2/neu</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>L-Lactate Dehydrogenase - biosynthesis</subject><subject>lung carcinoma</subject><subject>Lung Neoplasms - diagnosis</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - mortality</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Phosphopyruvate Hydratase - biosynthesis</subject><subject>Pneumology</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Protein Structure, Tertiary</subject><subject>Receptor, ErbB-2 - biosynthesis</subject><subject>Sex Factors</subject><subject>small‐cell lung cancer</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFqGzEQhkVIaRynkCcIOoTSy7oaSbtaHRvjpg6BXuLzotXOOgrrXVdjk-aWR8gz9kki14bmEnoa0Hz8__CJsXMQExBCfg0PfgJS2iM2AmFNJiTkx2yUViIzoIoTdkr0IARALvRHdgKghC6MHbGF__P8grG-SkPy2e91RKIw9Dz0nFau69K7x67j3bZfcu96j5EH4o5o8MFtsOGPYXPP18MQ-ToOy36gQGfsQ-s6wk-HOWaL77O76Y_s9uf1fPrtNvMawGbWS18bbazCprRNbQGx8d5qBa3WUKDUWig0ddkClhKUV21d5wKkKzRaqcbs8z43Nf_aIm2qVaDdua7HYUuVMSJXoMr_gmDKQtpSJPDLHvRxIIrYVusYVi4-VSCqnesqua52rhN6ccjc1its_oEHuQm4PACOvOvamOwFehNYpr_JE5btscfQ4dO7fdX8Zvq39xVqcpae</recordid><startdate>20010515</startdate><enddate>20010515</enddate><creator>Micke, Patrick</creator><creator>Hengstler, Jan Georg</creator><creator>Ros, Roser</creator><creator>Bittinger, Fernando</creator><creator>Metz, Tsegay</creator><creator>Gebhard, Susanne</creator><creator>Beeh, Kai Michael</creator><creator>Oesch, Franz</creator><creator>Buhl, Roland</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20010515</creationdate><title>c‐erbB‐2 Expression in small‐cell lung cancer is associated with poor prognosis</title><author>Micke, Patrick ; Hengstler, Jan Georg ; Ros, Roser ; Bittinger, Fernando ; Metz, Tsegay ; Gebhard, Susanne ; Beeh, Kai Michael ; Oesch, Franz ; Buhl, Roland</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4119-9c2cb74793ed89db91eedcc9431f4416e24403e7b8f1e8213c3fbb5012a64e923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Age Factors</topic><topic>Aged</topic><topic>Antibodies, Monoclonal - metabolism</topic><topic>Biological and medical sciences</topic><topic>c-erbB-2 gene</topic><topic>Carcinoma, Small Cell - diagnosis</topic><topic>Carcinoma, Small Cell - metabolism</topic><topic>Carcinoma, Small Cell - mortality</topic><topic>c‐erbB‐2</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>HER‐2/neu</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>L-Lactate Dehydrogenase - biosynthesis</topic><topic>lung carcinoma</topic><topic>Lung Neoplasms - diagnosis</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - mortality</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Phosphopyruvate Hydratase - biosynthesis</topic><topic>Pneumology</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Protein Structure, Tertiary</topic><topic>Receptor, ErbB-2 - biosynthesis</topic><topic>Sex Factors</topic><topic>small‐cell lung cancer</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Micke, Patrick</creatorcontrib><creatorcontrib>Hengstler, Jan Georg</creatorcontrib><creatorcontrib>Ros, Roser</creatorcontrib><creatorcontrib>Bittinger, Fernando</creatorcontrib><creatorcontrib>Metz, Tsegay</creatorcontrib><creatorcontrib>Gebhard, Susanne</creatorcontrib><creatorcontrib>Beeh, Kai Michael</creatorcontrib><creatorcontrib>Oesch, Franz</creatorcontrib><creatorcontrib>Buhl, Roland</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Micke, Patrick</au><au>Hengstler, Jan Georg</au><au>Ros, Roser</au><au>Bittinger, Fernando</au><au>Metz, Tsegay</au><au>Gebhard, Susanne</au><au>Beeh, Kai Michael</au><au>Oesch, Franz</au><au>Buhl, Roland</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>c‐erbB‐2 Expression in small‐cell lung cancer is associated with poor prognosis</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2001-05-15</date><risdate>2001</risdate><volume>92</volume><issue>4</issue><spage>474</spage><epage>479</epage><pages>474-479</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>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.</abstract><cop>New York</cop><pub>John Wiley & 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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