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Subtype-specific KRAS mutations in advanced lung adenocarcinoma: A retrospective study of patients treated with platinum-based chemotherapy
Abstract Background Platinum-based chemotherapy is the most common treatment in advanced-stage lung adenocarcinoma. Because the clinical significance of KRAS mutational status in this setting has not yet been clearly determined, a mutation subtype-specific analysis was performed in the so far larges...
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Published in: | European journal of cancer (1990) 2014-07, Vol.50 (10), p.1819-1828 |
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creator | Cserepes, Mihaly Ostoros, Gyula Lohinai, Zoltan Raso, Erzsebet Barbai, Tamas Timar, Jozsef Rozsas, Anita Moldvay, Judit Kovalszky, Ilona Fabian, Katalin Gyulai, Marton Ghanim, Bahil Laszlo, Viktoria Klikovits, Thomas Hoda, Mir Alireza Grusch, Michael Berger, Walter Klepetko, Walter Hegedus, Balazs Dome, Balazs |
description | Abstract Background Platinum-based chemotherapy is the most common treatment in advanced-stage lung adenocarcinoma. Because the clinical significance of KRAS mutational status in this setting has not yet been clearly determined, a mutation subtype-specific analysis was performed in the so far largest cohort of Caucasian patients with KRAS mutant advanced-stage lung adenocarcinoma treated with platinum-based chemotherapy. Methods 505 Caucasian stage III–IV lung adenocarcinoma patients with known amino acid substitution-specific KRAS mutational status and treated with platinum-based chemotherapy were included. The correlations of subtype-specific KRAS mutations with smoking status, progression-free and overall survival (PFS and OS, respectively) and therapeutic response were analysed. Results Among 338 KRAS wild-type, 147 codon 12 mutant and 20 codon 13 mutant patients, there were no mutation-related significant differences in PFS or OS ( P values were 0.534 and 0.917, respectively). Eastern Cooperative Oncology Group (ECOG) status and clinical stage were significant independent prognostic factors. KRAS mutation showed a significant correlation with smoking status ( P = 0.018). Importantly, however, G12V KRAS mutant patients were significantly more frequent among never-smokers than all other codon 12 KRAS mutant (G12x) subtypes ( P = 0.016). Furthermore, this subgroup tended to have a higher response rate (66% versus 47%; P = 0.077). A modestly longer median PFS was also found in the G12V mutant cohort (233 days; versus 175 days in the G12x group; P = 0.145). Conclusions While KRAS mutation status per se is neither prognostic nor predictive in stage III–IV lung adenocarcinoma, subtype-specific analysis may indeed identify clinically relevant subgroups of patients that may ultimately influence treatment decisions. |
doi_str_mv | 10.1016/j.ejca.2014.04.001 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1531954490</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0959804914005656</els_id><sourcerecordid>1531954490</sourcerecordid><originalsourceid>FETCH-LOGICAL-c485t-423be350c4429d7c22402cda3638145102be36168a88252e7155820a95ca36343</originalsourceid><addsrcrecordid>eNp9kt2q1DAUhYsonvHoC3ghuRG86biTJm0qIgwH__CA4Oh1yKS7Tmqb1iQd6TP40qbMqOCFEAjZ-dZOslay7DGFLQVaPu-22Bm9ZUD5FtIAeifbUFnVOUjB7mYbqEWdS-D1VfYghA4AKsnhfnbFeFXKgtWb7Od-PsRlwjxMaGxrDfnwabcnwxx1tKMLxDqim5N2BhvSz-5rWqEbjfbGunHQL8iOeIx-XPXRnpCEODcLGVsypQ7oYiDRo45J_sPGI5n6VHbzkB90SDVzxGGMR_R6Wh5m91rdB3x0ma-zL29ef755l99-fPv-ZnebGy5FzDkrDlgIMJyzuqkMYxyYaXRRFpJyQYGl7ZKWUkvJBMOKCiEZ6FqYleHFdfbs3Hfy4_cZQ1SDDQb7Xjsc56CoKGgtOK8hoeyMmvTC4LFVk7eD9ouioNYQVKfWENQagoI0gCbRk0v_-TBg80fy2_UEPL0AOhjdtz7Za8NfLqUnqoIl7uWZw-TGyaJXwSRLUxTWJ7dVM9r_3-PVP3LTW2fTid9wwdCNs3fJZ0VVYArUfv0u62-hHECUoix-AUqjuvM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1531954490</pqid></control><display><type>article</type><title>Subtype-specific KRAS mutations in advanced lung adenocarcinoma: A retrospective study of patients treated with platinum-based chemotherapy</title><source>Elsevier</source><creator>Cserepes, Mihaly ; Ostoros, Gyula ; Lohinai, Zoltan ; Raso, Erzsebet ; Barbai, Tamas ; Timar, Jozsef ; Rozsas, Anita ; Moldvay, Judit ; Kovalszky, Ilona ; Fabian, Katalin ; Gyulai, Marton ; Ghanim, Bahil ; Laszlo, Viktoria ; Klikovits, Thomas ; Hoda, Mir Alireza ; Grusch, Michael ; Berger, Walter ; Klepetko, Walter ; Hegedus, Balazs ; Dome, Balazs</creator><creatorcontrib>Cserepes, Mihaly ; Ostoros, Gyula ; Lohinai, Zoltan ; Raso, Erzsebet ; Barbai, Tamas ; Timar, Jozsef ; Rozsas, Anita ; Moldvay, Judit ; Kovalszky, Ilona ; Fabian, Katalin ; Gyulai, Marton ; Ghanim, Bahil ; Laszlo, Viktoria ; Klikovits, Thomas ; Hoda, Mir Alireza ; Grusch, Michael ; Berger, Walter ; Klepetko, Walter ; Hegedus, Balazs ; Dome, Balazs</creatorcontrib><description>Abstract Background Platinum-based chemotherapy is the most common treatment in advanced-stage lung adenocarcinoma. Because the clinical significance of KRAS mutational status in this setting has not yet been clearly determined, a mutation subtype-specific analysis was performed in the so far largest cohort of Caucasian patients with KRAS mutant advanced-stage lung adenocarcinoma treated with platinum-based chemotherapy. Methods 505 Caucasian stage III–IV lung adenocarcinoma patients with known amino acid substitution-specific KRAS mutational status and treated with platinum-based chemotherapy were included. The correlations of subtype-specific KRAS mutations with smoking status, progression-free and overall survival (PFS and OS, respectively) and therapeutic response were analysed. Results Among 338 KRAS wild-type, 147 codon 12 mutant and 20 codon 13 mutant patients, there were no mutation-related significant differences in PFS or OS ( P values were 0.534 and 0.917, respectively). Eastern Cooperative Oncology Group (ECOG) status and clinical stage were significant independent prognostic factors. KRAS mutation showed a significant correlation with smoking status ( P = 0.018). Importantly, however, G12V KRAS mutant patients were significantly more frequent among never-smokers than all other codon 12 KRAS mutant (G12x) subtypes ( P = 0.016). Furthermore, this subgroup tended to have a higher response rate (66% versus 47%; P = 0.077). A modestly longer median PFS was also found in the G12V mutant cohort (233 days; versus 175 days in the G12x group; P = 0.145). Conclusions While KRAS mutation status per se is neither prognostic nor predictive in stage III–IV lung adenocarcinoma, subtype-specific analysis may indeed identify clinically relevant subgroups of patients that may ultimately influence treatment decisions.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2014.04.001</identifier><identifier>PMID: 24768329</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Adenocarcinoma - drug therapy ; Adenocarcinoma - ethnology ; Adenocarcinoma - genetics ; Adenocarcinoma - mortality ; Adenocarcinoma - pathology ; Adenocarcinoma of Lung ; Adult ; Advanced-stage lung adenocarcinoma ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Carboplatin - administration & dosage ; Chi-Square Distribution ; Cisplatin - administration & dosage ; Disease-Free Survival ; DNA Mutational Analysis ; European Continental Ancestry Group - genetics ; Female ; Genetic Predisposition to Disease ; Hematology, Oncology and Palliative Medicine ; Humans ; Hungary - epidemiology ; Kaplan-Meier Estimate ; KRAS mutation ; Lung Neoplasms - drug therapy ; Lung Neoplasms - ethnology ; Lung Neoplasms - genetics ; Lung Neoplasms - mortality ; Lung Neoplasms - pathology ; Male ; Medical sciences ; Middle Aged ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Multivariate Analysis ; Mutation ; Neoplasm Staging ; Non-small cell lung cancer ; Patient Selection ; Pharmacology. Drug treatments ; Phenotype ; Platinum-based chemotherapy ; Pneumology ; Proportional Hazards Models ; Proto-Oncogene Proteins - genetics ; Proto-Oncogene Proteins p21(ras) ; ras Proteins - genetics ; Retrospective Studies ; Risk Factors ; Smoking - adverse effects ; Smoking - ethnology ; Time Factors ; Treatment Outcome ; Tumors ; Tumors of the respiratory system and mediastinum</subject><ispartof>European journal of cancer (1990), 2014-07, Vol.50 (10), p.1819-1828</ispartof><rights>The Authors</rights><rights>2014 The Authors</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-423be350c4429d7c22402cda3638145102be36168a88252e7155820a95ca36343</citedby><cites>FETCH-LOGICAL-c485t-423be350c4429d7c22402cda3638145102be36168a88252e7155820a95ca36343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28525732$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24768329$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cserepes, Mihaly</creatorcontrib><creatorcontrib>Ostoros, Gyula</creatorcontrib><creatorcontrib>Lohinai, Zoltan</creatorcontrib><creatorcontrib>Raso, Erzsebet</creatorcontrib><creatorcontrib>Barbai, Tamas</creatorcontrib><creatorcontrib>Timar, Jozsef</creatorcontrib><creatorcontrib>Rozsas, Anita</creatorcontrib><creatorcontrib>Moldvay, Judit</creatorcontrib><creatorcontrib>Kovalszky, Ilona</creatorcontrib><creatorcontrib>Fabian, Katalin</creatorcontrib><creatorcontrib>Gyulai, Marton</creatorcontrib><creatorcontrib>Ghanim, Bahil</creatorcontrib><creatorcontrib>Laszlo, Viktoria</creatorcontrib><creatorcontrib>Klikovits, Thomas</creatorcontrib><creatorcontrib>Hoda, Mir Alireza</creatorcontrib><creatorcontrib>Grusch, Michael</creatorcontrib><creatorcontrib>Berger, Walter</creatorcontrib><creatorcontrib>Klepetko, Walter</creatorcontrib><creatorcontrib>Hegedus, Balazs</creatorcontrib><creatorcontrib>Dome, Balazs</creatorcontrib><title>Subtype-specific KRAS mutations in advanced lung adenocarcinoma: A retrospective study of patients treated with platinum-based chemotherapy</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Abstract Background Platinum-based chemotherapy is the most common treatment in advanced-stage lung adenocarcinoma. Because the clinical significance of KRAS mutational status in this setting has not yet been clearly determined, a mutation subtype-specific analysis was performed in the so far largest cohort of Caucasian patients with KRAS mutant advanced-stage lung adenocarcinoma treated with platinum-based chemotherapy. Methods 505 Caucasian stage III–IV lung adenocarcinoma patients with known amino acid substitution-specific KRAS mutational status and treated with platinum-based chemotherapy were included. The correlations of subtype-specific KRAS mutations with smoking status, progression-free and overall survival (PFS and OS, respectively) and therapeutic response were analysed. Results Among 338 KRAS wild-type, 147 codon 12 mutant and 20 codon 13 mutant patients, there were no mutation-related significant differences in PFS or OS ( P values were 0.534 and 0.917, respectively). Eastern Cooperative Oncology Group (ECOG) status and clinical stage were significant independent prognostic factors. KRAS mutation showed a significant correlation with smoking status ( P = 0.018). Importantly, however, G12V KRAS mutant patients were significantly more frequent among never-smokers than all other codon 12 KRAS mutant (G12x) subtypes ( P = 0.016). Furthermore, this subgroup tended to have a higher response rate (66% versus 47%; P = 0.077). A modestly longer median PFS was also found in the G12V mutant cohort (233 days; versus 175 days in the G12x group; P = 0.145). Conclusions While KRAS mutation status per se is neither prognostic nor predictive in stage III–IV lung adenocarcinoma, subtype-specific analysis may indeed identify clinically relevant subgroups of patients that may ultimately influence treatment decisions.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - ethnology</subject><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma of Lung</subject><subject>Adult</subject><subject>Advanced-stage lung adenocarcinoma</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Carboplatin - administration & dosage</subject><subject>Chi-Square Distribution</subject><subject>Cisplatin - administration & dosage</subject><subject>Disease-Free Survival</subject><subject>DNA Mutational Analysis</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Hungary - epidemiology</subject><subject>Kaplan-Meier Estimate</subject><subject>KRAS mutation</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - ethnology</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - mortality</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Multivariate Analysis</subject><subject>Mutation</subject><subject>Neoplasm Staging</subject><subject>Non-small cell lung cancer</subject><subject>Patient Selection</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenotype</subject><subject>Platinum-based chemotherapy</subject><subject>Pneumology</subject><subject>Proportional Hazards Models</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Proto-Oncogene Proteins p21(ras)</subject><subject>ras Proteins - genetics</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Smoking - adverse effects</subject><subject>Smoking - ethnology</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9kt2q1DAUhYsonvHoC3ghuRG86biTJm0qIgwH__CA4Oh1yKS7Tmqb1iQd6TP40qbMqOCFEAjZ-dZOslay7DGFLQVaPu-22Bm9ZUD5FtIAeifbUFnVOUjB7mYbqEWdS-D1VfYghA4AKsnhfnbFeFXKgtWb7Od-PsRlwjxMaGxrDfnwabcnwxx1tKMLxDqim5N2BhvSz-5rWqEbjfbGunHQL8iOeIx-XPXRnpCEODcLGVsypQ7oYiDRo45J_sPGI5n6VHbzkB90SDVzxGGMR_R6Wh5m91rdB3x0ma-zL29ef755l99-fPv-ZnebGy5FzDkrDlgIMJyzuqkMYxyYaXRRFpJyQYGl7ZKWUkvJBMOKCiEZ6FqYleHFdfbs3Hfy4_cZQ1SDDQb7Xjsc56CoKGgtOK8hoeyMmvTC4LFVk7eD9ouioNYQVKfWENQagoI0gCbRk0v_-TBg80fy2_UEPL0AOhjdtz7Za8NfLqUnqoIl7uWZw-TGyaJXwSRLUxTWJ7dVM9r_3-PVP3LTW2fTid9wwdCNs3fJZ0VVYArUfv0u62-hHECUoix-AUqjuvM</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Cserepes, Mihaly</creator><creator>Ostoros, Gyula</creator><creator>Lohinai, Zoltan</creator><creator>Raso, Erzsebet</creator><creator>Barbai, Tamas</creator><creator>Timar, Jozsef</creator><creator>Rozsas, Anita</creator><creator>Moldvay, Judit</creator><creator>Kovalszky, Ilona</creator><creator>Fabian, Katalin</creator><creator>Gyulai, Marton</creator><creator>Ghanim, Bahil</creator><creator>Laszlo, Viktoria</creator><creator>Klikovits, Thomas</creator><creator>Hoda, Mir Alireza</creator><creator>Grusch, Michael</creator><creator>Berger, Walter</creator><creator>Klepetko, Walter</creator><creator>Hegedus, Balazs</creator><creator>Dome, Balazs</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope></search><sort><creationdate>20140701</creationdate><title>Subtype-specific KRAS mutations in advanced lung adenocarcinoma: A retrospective study of patients treated with platinum-based chemotherapy</title><author>Cserepes, Mihaly ; Ostoros, Gyula ; Lohinai, Zoltan ; Raso, Erzsebet ; Barbai, Tamas ; Timar, Jozsef ; Rozsas, Anita ; Moldvay, Judit ; Kovalszky, Ilona ; Fabian, Katalin ; Gyulai, Marton ; Ghanim, Bahil ; Laszlo, Viktoria ; Klikovits, Thomas ; Hoda, Mir Alireza ; Grusch, Michael ; Berger, Walter ; Klepetko, Walter ; Hegedus, Balazs ; Dome, Balazs</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-423be350c4429d7c22402cda3638145102be36168a88252e7155820a95ca36343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adenocarcinoma - drug therapy</topic><topic>Adenocarcinoma - ethnology</topic><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma of Lung</topic><topic>Adult</topic><topic>Advanced-stage lung adenocarcinoma</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Carboplatin - administration & dosage</topic><topic>Chi-Square Distribution</topic><topic>Cisplatin - administration & dosage</topic><topic>Disease-Free Survival</topic><topic>DNA Mutational Analysis</topic><topic>European Continental Ancestry Group - genetics</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Hungary - epidemiology</topic><topic>Kaplan-Meier Estimate</topic><topic>KRAS mutation</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - ethnology</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - mortality</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Multivariate Analysis</topic><topic>Mutation</topic><topic>Neoplasm Staging</topic><topic>Non-small cell lung cancer</topic><topic>Patient Selection</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenotype</topic><topic>Platinum-based chemotherapy</topic><topic>Pneumology</topic><topic>Proportional Hazards Models</topic><topic>Proto-Oncogene Proteins - genetics</topic><topic>Proto-Oncogene Proteins p21(ras)</topic><topic>ras Proteins - genetics</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Smoking - adverse effects</topic><topic>Smoking - ethnology</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cserepes, Mihaly</creatorcontrib><creatorcontrib>Ostoros, Gyula</creatorcontrib><creatorcontrib>Lohinai, Zoltan</creatorcontrib><creatorcontrib>Raso, Erzsebet</creatorcontrib><creatorcontrib>Barbai, Tamas</creatorcontrib><creatorcontrib>Timar, Jozsef</creatorcontrib><creatorcontrib>Rozsas, Anita</creatorcontrib><creatorcontrib>Moldvay, Judit</creatorcontrib><creatorcontrib>Kovalszky, Ilona</creatorcontrib><creatorcontrib>Fabian, Katalin</creatorcontrib><creatorcontrib>Gyulai, Marton</creatorcontrib><creatorcontrib>Ghanim, Bahil</creatorcontrib><creatorcontrib>Laszlo, Viktoria</creatorcontrib><creatorcontrib>Klikovits, Thomas</creatorcontrib><creatorcontrib>Hoda, Mir Alireza</creatorcontrib><creatorcontrib>Grusch, Michael</creatorcontrib><creatorcontrib>Berger, Walter</creatorcontrib><creatorcontrib>Klepetko, Walter</creatorcontrib><creatorcontrib>Hegedus, Balazs</creatorcontrib><creatorcontrib>Dome, Balazs</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>MEDLINE - Academic</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cserepes, Mihaly</au><au>Ostoros, Gyula</au><au>Lohinai, Zoltan</au><au>Raso, Erzsebet</au><au>Barbai, Tamas</au><au>Timar, Jozsef</au><au>Rozsas, Anita</au><au>Moldvay, Judit</au><au>Kovalszky, Ilona</au><au>Fabian, Katalin</au><au>Gyulai, Marton</au><au>Ghanim, Bahil</au><au>Laszlo, Viktoria</au><au>Klikovits, Thomas</au><au>Hoda, Mir Alireza</au><au>Grusch, Michael</au><au>Berger, Walter</au><au>Klepetko, Walter</au><au>Hegedus, Balazs</au><au>Dome, Balazs</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subtype-specific KRAS mutations in advanced lung adenocarcinoma: A retrospective study of patients treated with platinum-based chemotherapy</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>50</volume><issue>10</issue><spage>1819</spage><epage>1828</epage><pages>1819-1828</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Abstract Background Platinum-based chemotherapy is the most common treatment in advanced-stage lung adenocarcinoma. Because the clinical significance of KRAS mutational status in this setting has not yet been clearly determined, a mutation subtype-specific analysis was performed in the so far largest cohort of Caucasian patients with KRAS mutant advanced-stage lung adenocarcinoma treated with platinum-based chemotherapy. Methods 505 Caucasian stage III–IV lung adenocarcinoma patients with known amino acid substitution-specific KRAS mutational status and treated with platinum-based chemotherapy were included. The correlations of subtype-specific KRAS mutations with smoking status, progression-free and overall survival (PFS and OS, respectively) and therapeutic response were analysed. Results Among 338 KRAS wild-type, 147 codon 12 mutant and 20 codon 13 mutant patients, there were no mutation-related significant differences in PFS or OS ( P values were 0.534 and 0.917, respectively). Eastern Cooperative Oncology Group (ECOG) status and clinical stage were significant independent prognostic factors. KRAS mutation showed a significant correlation with smoking status ( P = 0.018). Importantly, however, G12V KRAS mutant patients were significantly more frequent among never-smokers than all other codon 12 KRAS mutant (G12x) subtypes ( P = 0.016). Furthermore, this subgroup tended to have a higher response rate (66% versus 47%; P = 0.077). A modestly longer median PFS was also found in the G12V mutant cohort (233 days; versus 175 days in the G12x group; P = 0.145). Conclusions While KRAS mutation status per se is neither prognostic nor predictive in stage III–IV lung adenocarcinoma, subtype-specific analysis may indeed identify clinically relevant subgroups of patients that may ultimately influence treatment decisions.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>24768329</pmid><doi>10.1016/j.ejca.2014.04.001</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - drug therapy Adenocarcinoma - ethnology Adenocarcinoma - genetics Adenocarcinoma - mortality Adenocarcinoma - pathology Adenocarcinoma of Lung Adult Advanced-stage lung adenocarcinoma Aged Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Carboplatin - administration & dosage Chi-Square Distribution Cisplatin - administration & dosage Disease-Free Survival DNA Mutational Analysis European Continental Ancestry Group - genetics Female Genetic Predisposition to Disease Hematology, Oncology and Palliative Medicine Humans Hungary - epidemiology Kaplan-Meier Estimate KRAS mutation Lung Neoplasms - drug therapy Lung Neoplasms - ethnology Lung Neoplasms - genetics Lung Neoplasms - mortality Lung Neoplasms - pathology Male Medical sciences Middle Aged Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Multivariate Analysis Mutation Neoplasm Staging Non-small cell lung cancer Patient Selection Pharmacology. Drug treatments Phenotype Platinum-based chemotherapy Pneumology Proportional Hazards Models Proto-Oncogene Proteins - genetics Proto-Oncogene Proteins p21(ras) ras Proteins - genetics Retrospective Studies Risk Factors Smoking - adverse effects Smoking - ethnology Time Factors Treatment Outcome Tumors Tumors of the respiratory system and mediastinum |
title | Subtype-specific KRAS mutations in advanced lung adenocarcinoma: A retrospective study of patients treated with platinum-based chemotherapy |
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