Association between Tumor Epidermal Growth Factor Receptor Mutation and Pulmonary Tuberculosis in Patients with Adenocarcinoma of the Lungs
The possible association between pulmonary tuberculosis (TB) and lung cancer development has been studied for several decades. However, the association between epidermal growth factor receptor (EGFR) mutation status and pulmonary TB in patients with adenocarcinoma of the lungs is unknown. We reviewe...
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Veröffentlicht in: | Journal of thoracic oncology 2012-02, Vol.7 (2), p.299-305 |
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creator | Luo, Yung-Hung Wu, Chieh-Hung Wu, Wen-Shuo Huang, Chu-Yun Su, Wei-Juin Tsai, Chun-Ming Lee, Yu-Chin Perng, Reury-Perng Chen, Yuh-Min |
description | The possible association between pulmonary tuberculosis (TB) and lung cancer development has been studied for several decades. However, the association between epidermal growth factor receptor (EGFR) mutation status and pulmonary TB in patients with adenocarcinoma of the lungs is unknown.
We reviewed the data of our patients with adenocarcinoma of the lungs who had a clinical history of pulmonary TB or old TB lesions shown on chest computed tomography scan and evaluated the association between tumor EGFR mutation status and pulmonary TB.
From June 1999 to January 2011, there were 275 patients with pulmonary adenocarcinoma with tumor EGFR mutation data available for analysis. Of them, 191 patients had EGFR mutations, 17 had a clinical history of pulmonary TB infection, 72 had old TB lesions on chest computed tomography scans, and 14 had scar cancer. Patients with old TB lesions had a higher incidence of EGFR mutation than those without (p = 0.018). Exon 19 deletions occurred more frequently in patients with old TB lesions than in patients without (p < 0.001). Those patients with old TB lesions who had EGFR mutations or exon 19 mutations survived longer than those who did not (p = 0.014 and 0.001, respectively). Patients with exon 19 deletions and old TB lesions showed no survival difference compared with those with exon 19 deletions and without old TB lesions (p = 0.271).
Patients with pulmonary adenocarcinoma who had scar cancer or had old TB lesions had a higher probability of having EGFR mutations, especially exon 19 deletions. |
doi_str_mv | 10.1097/JTO.0b013e31823c588d |
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We reviewed the data of our patients with adenocarcinoma of the lungs who had a clinical history of pulmonary TB or old TB lesions shown on chest computed tomography scan and evaluated the association between tumor EGFR mutation status and pulmonary TB.
From June 1999 to January 2011, there were 275 patients with pulmonary adenocarcinoma with tumor EGFR mutation data available for analysis. Of them, 191 patients had EGFR mutations, 17 had a clinical history of pulmonary TB infection, 72 had old TB lesions on chest computed tomography scans, and 14 had scar cancer. Patients with old TB lesions had a higher incidence of EGFR mutation than those without (p = 0.018). Exon 19 deletions occurred more frequently in patients with old TB lesions than in patients without (p < 0.001). Those patients with old TB lesions who had EGFR mutations or exon 19 mutations survived longer than those who did not (p = 0.014 and 0.001, respectively). Patients with exon 19 deletions and old TB lesions showed no survival difference compared with those with exon 19 deletions and without old TB lesions (p = 0.271).
Patients with pulmonary adenocarcinoma who had scar cancer or had old TB lesions had a higher probability of having EGFR mutations, especially exon 19 deletions.</description><identifier>ISSN: 1556-0864</identifier><identifier>EISSN: 1556-1380</identifier><identifier>DOI: 10.1097/JTO.0b013e31823c588d</identifier><identifier>PMID: 22173705</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenocarcinoma - complications ; Adenocarcinoma - genetics ; Adenocarcinoma - mortality ; Adult ; Aged ; Aged, 80 and over ; Epidermal growth factor receptor ; Exons - genetics ; Female ; Humans ; Lung Neoplasms - complications ; Lung Neoplasms - genetics ; Lung Neoplasms - mortality ; Male ; Middle Aged ; Mutation - genetics ; Non-small cell lung cancer ; Prognosis ; Receptor, Epidermal Growth Factor - genetics ; Retrospective Studies ; Sequence Deletion ; Survival Rate ; Tuberculosis ; Tuberculosis, Pulmonary - etiology ; Tuberculosis, Pulmonary - genetics ; Tuberculosis, Pulmonary - mortality</subject><ispartof>Journal of thoracic oncology, 2012-02, Vol.7 (2), p.299-305</ispartof><rights>2012 International Association for the Study of Lung Cancer</rights><rights>2012International Association for the Study of Lung Cancer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456d-822b03c1ccf1d4f17c97598693ef9fe8e156bfb14c9c74bd55aab4e256caa8343</citedby><cites>FETCH-LOGICAL-c456d-822b03c1ccf1d4f17c97598693ef9fe8e156bfb14c9c74bd55aab4e256caa8343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22173705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, Yung-Hung</creatorcontrib><creatorcontrib>Wu, Chieh-Hung</creatorcontrib><creatorcontrib>Wu, Wen-Shuo</creatorcontrib><creatorcontrib>Huang, Chu-Yun</creatorcontrib><creatorcontrib>Su, Wei-Juin</creatorcontrib><creatorcontrib>Tsai, Chun-Ming</creatorcontrib><creatorcontrib>Lee, Yu-Chin</creatorcontrib><creatorcontrib>Perng, Reury-Perng</creatorcontrib><creatorcontrib>Chen, Yuh-Min</creatorcontrib><title>Association between Tumor Epidermal Growth Factor Receptor Mutation and Pulmonary Tuberculosis in Patients with Adenocarcinoma of the Lungs</title><title>Journal of thoracic oncology</title><addtitle>J Thorac Oncol</addtitle><description>The possible association between pulmonary tuberculosis (TB) and lung cancer development has been studied for several decades. However, the association between epidermal growth factor receptor (EGFR) mutation status and pulmonary TB in patients with adenocarcinoma of the lungs is unknown.
We reviewed the data of our patients with adenocarcinoma of the lungs who had a clinical history of pulmonary TB or old TB lesions shown on chest computed tomography scan and evaluated the association between tumor EGFR mutation status and pulmonary TB.
From June 1999 to January 2011, there were 275 patients with pulmonary adenocarcinoma with tumor EGFR mutation data available for analysis. Of them, 191 patients had EGFR mutations, 17 had a clinical history of pulmonary TB infection, 72 had old TB lesions on chest computed tomography scans, and 14 had scar cancer. Patients with old TB lesions had a higher incidence of EGFR mutation than those without (p = 0.018). Exon 19 deletions occurred more frequently in patients with old TB lesions than in patients without (p < 0.001). Those patients with old TB lesions who had EGFR mutations or exon 19 mutations survived longer than those who did not (p = 0.014 and 0.001, respectively). Patients with exon 19 deletions and old TB lesions showed no survival difference compared with those with exon 19 deletions and without old TB lesions (p = 0.271).
Patients with pulmonary adenocarcinoma who had scar cancer or had old TB lesions had a higher probability of having EGFR mutations, especially exon 19 deletions.</description><subject>Adenocarcinoma - complications</subject><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - mortality</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Epidermal growth factor receptor</subject><subject>Exons - genetics</subject><subject>Female</subject><subject>Humans</subject><subject>Lung Neoplasms - complications</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - mortality</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation - genetics</subject><subject>Non-small cell lung cancer</subject><subject>Prognosis</subject><subject>Receptor, Epidermal Growth Factor - genetics</subject><subject>Retrospective Studies</subject><subject>Sequence Deletion</subject><subject>Survival Rate</subject><subject>Tuberculosis</subject><subject>Tuberculosis, Pulmonary - etiology</subject><subject>Tuberculosis, Pulmonary - genetics</subject><subject>Tuberculosis, Pulmonary - mortality</subject><issn>1556-0864</issn><issn>1556-1380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhSMEoj_wBgh5x2qKHduJs0EaVf0BTdUKDevIub5hDIk92E4jnqEvjasMLLooK19Z5ztX95yieMfoGaNN_fHL9vaMdpRx5EyVHKRS5kVxzKSsVowr-vIwU1WJo-Ikxh-UCkmFel0clSWreU3lcfGwjtGD1cl6RzpMM6Ij22n0gVzsrcEw6oFcBT-nHbnUkPL_VwTcPw43U1o47Qy5m4bROx1-Z7rDANPgo43EOnKXRehSJLPNJmuDzoMOYJ0fNfE9STskm8l9j2-KV70eIr49vKfFt8uL7fn1anN79fl8vVmBkJVZqbLsKAcG0DMjelZDU8tGVQ3HvulRIZNV13dMQAO16IyUWncCS1mB1ooLflp8WHz3wf-aMKZ2tBFwGLRDP8W2YZWSnNIyK8WihOBjDNi3-2DHfGTLaPvYQptbaJ-2kLH3hwVTN6L5B_2NPQvUIpj9kDDEn8M0Y2h3qIe0-5_3pwXFnNC9zVSEHC-gsQEhtcbb5w3-ALUzrgs</recordid><startdate>201202</startdate><enddate>201202</enddate><creator>Luo, Yung-Hung</creator><creator>Wu, Chieh-Hung</creator><creator>Wu, Wen-Shuo</creator><creator>Huang, Chu-Yun</creator><creator>Su, Wei-Juin</creator><creator>Tsai, Chun-Ming</creator><creator>Lee, Yu-Chin</creator><creator>Perng, Reury-Perng</creator><creator>Chen, Yuh-Min</creator><general>Elsevier Inc</general><general>International Association for the Study of Lung Cancer</general><scope>6I.</scope><scope>AAFTH</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>201202</creationdate><title>Association between Tumor Epidermal Growth Factor Receptor Mutation and Pulmonary Tuberculosis in Patients with Adenocarcinoma of the Lungs</title><author>Luo, Yung-Hung ; Wu, Chieh-Hung ; Wu, Wen-Shuo ; Huang, Chu-Yun ; Su, Wei-Juin ; Tsai, Chun-Ming ; Lee, Yu-Chin ; Perng, Reury-Perng ; Chen, Yuh-Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456d-822b03c1ccf1d4f17c97598693ef9fe8e156bfb14c9c74bd55aab4e256caa8343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adenocarcinoma - complications</topic><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - mortality</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Epidermal growth factor receptor</topic><topic>Exons - genetics</topic><topic>Female</topic><topic>Humans</topic><topic>Lung Neoplasms - complications</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - mortality</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation - genetics</topic><topic>Non-small cell lung cancer</topic><topic>Prognosis</topic><topic>Receptor, Epidermal Growth Factor - genetics</topic><topic>Retrospective Studies</topic><topic>Sequence Deletion</topic><topic>Survival Rate</topic><topic>Tuberculosis</topic><topic>Tuberculosis, Pulmonary - etiology</topic><topic>Tuberculosis, Pulmonary - genetics</topic><topic>Tuberculosis, Pulmonary - mortality</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Yung-Hung</creatorcontrib><creatorcontrib>Wu, Chieh-Hung</creatorcontrib><creatorcontrib>Wu, Wen-Shuo</creatorcontrib><creatorcontrib>Huang, Chu-Yun</creatorcontrib><creatorcontrib>Su, Wei-Juin</creatorcontrib><creatorcontrib>Tsai, Chun-Ming</creatorcontrib><creatorcontrib>Lee, Yu-Chin</creatorcontrib><creatorcontrib>Perng, Reury-Perng</creatorcontrib><creatorcontrib>Chen, Yuh-Min</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Journal of thoracic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Yung-Hung</au><au>Wu, Chieh-Hung</au><au>Wu, Wen-Shuo</au><au>Huang, Chu-Yun</au><au>Su, Wei-Juin</au><au>Tsai, Chun-Ming</au><au>Lee, Yu-Chin</au><au>Perng, Reury-Perng</au><au>Chen, Yuh-Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between Tumor Epidermal Growth Factor Receptor Mutation and Pulmonary Tuberculosis in Patients with Adenocarcinoma of the Lungs</atitle><jtitle>Journal of thoracic oncology</jtitle><addtitle>J Thorac Oncol</addtitle><date>2012-02</date><risdate>2012</risdate><volume>7</volume><issue>2</issue><spage>299</spage><epage>305</epage><pages>299-305</pages><issn>1556-0864</issn><eissn>1556-1380</eissn><abstract>The possible association between pulmonary tuberculosis (TB) and lung cancer development has been studied for several decades. However, the association between epidermal growth factor receptor (EGFR) mutation status and pulmonary TB in patients with adenocarcinoma of the lungs is unknown.
We reviewed the data of our patients with adenocarcinoma of the lungs who had a clinical history of pulmonary TB or old TB lesions shown on chest computed tomography scan and evaluated the association between tumor EGFR mutation status and pulmonary TB.
From June 1999 to January 2011, there were 275 patients with pulmonary adenocarcinoma with tumor EGFR mutation data available for analysis. Of them, 191 patients had EGFR mutations, 17 had a clinical history of pulmonary TB infection, 72 had old TB lesions on chest computed tomography scans, and 14 had scar cancer. Patients with old TB lesions had a higher incidence of EGFR mutation than those without (p = 0.018). Exon 19 deletions occurred more frequently in patients with old TB lesions than in patients without (p < 0.001). Those patients with old TB lesions who had EGFR mutations or exon 19 mutations survived longer than those who did not (p = 0.014 and 0.001, respectively). Patients with exon 19 deletions and old TB lesions showed no survival difference compared with those with exon 19 deletions and without old TB lesions (p = 0.271).
Patients with pulmonary adenocarcinoma who had scar cancer or had old TB lesions had a higher probability of having EGFR mutations, especially exon 19 deletions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22173705</pmid><doi>10.1097/JTO.0b013e31823c588d</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - complications Adenocarcinoma - genetics Adenocarcinoma - mortality Adult Aged Aged, 80 and over Epidermal growth factor receptor Exons - genetics Female Humans Lung Neoplasms - complications Lung Neoplasms - genetics Lung Neoplasms - mortality Male Middle Aged Mutation - genetics Non-small cell lung cancer Prognosis Receptor, Epidermal Growth Factor - genetics Retrospective Studies Sequence Deletion Survival Rate Tuberculosis Tuberculosis, Pulmonary - etiology Tuberculosis, Pulmonary - genetics Tuberculosis, Pulmonary - mortality |
title | Association between Tumor Epidermal Growth Factor Receptor Mutation and Pulmonary Tuberculosis in Patients with Adenocarcinoma of the Lungs |
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