EGFR mutation exists in squamous cell lung carcinoma
Whether EGFR mutation occurs in lung squamous cell carcinoma (SCC) remains a controversial issue. Although numerous trials have shown positive response to tyrosine kinase inhibitors in SCC, these observations have not been well correlated with presence or absence of EGFR mutation. A complicating iss...
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Veröffentlicht in: | Pathology 2020-04, Vol.52 (3), p.323-328 |
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description | Whether EGFR mutation occurs in lung squamous cell carcinoma (SCC) remains a controversial issue. Although numerous trials have shown positive response to tyrosine kinase inhibitors in SCC, these observations have not been well correlated with presence or absence of EGFR mutation. A complicating issue is that adenosquamous carcinoma, a mimic of SCC, frequently harbours EGFR mutations. We evaluated the EGFR mutation status of 191 cases initially diagnosed as SCC of lung origin in years 2000–2011, and performed a panel of markers including p40, p63, CK5/6, TTF-1, mucicarmine on the tissue microarray or tissue blocks from each case, to ascertain the squamous differentiation of each case. Four cases were found to have EGFR mutations, with three showing typical squamous morphological features and immunohistochemical profile on all available tumour blocks, and one reclassified as adenosquamous carcinoma. Mixed responses were noted for two of the patients with EGFR-mutated SCC treated with tyrosine kinase inhibitors. In conclusion, we report that a small subset of rigorously proven SCC harbours EGFR mutation. It also appears in our cohort that EGFR-mutated tumours, in the context of SCC, may have relatively poor response to tyrosine kinase inhibitors. |
doi_str_mv | 10.1016/j.pathol.2019.12.003 |
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Although numerous trials have shown positive response to tyrosine kinase inhibitors in SCC, these observations have not been well correlated with presence or absence of EGFR mutation. A complicating issue is that adenosquamous carcinoma, a mimic of SCC, frequently harbours EGFR mutations. We evaluated the EGFR mutation status of 191 cases initially diagnosed as SCC of lung origin in years 2000–2011, and performed a panel of markers including p40, p63, CK5/6, TTF-1, mucicarmine on the tissue microarray or tissue blocks from each case, to ascertain the squamous differentiation of each case. Four cases were found to have EGFR mutations, with three showing typical squamous morphological features and immunohistochemical profile on all available tumour blocks, and one reclassified as adenosquamous carcinoma. Mixed responses were noted for two of the patients with EGFR-mutated SCC treated with tyrosine kinase inhibitors. In conclusion, we report that a small subset of rigorously proven SCC harbours EGFR mutation. It also appears in our cohort that EGFR-mutated tumours, in the context of SCC, may have relatively poor response to tyrosine kinase inhibitors.</description><identifier>ISSN: 0031-3025</identifier><identifier>EISSN: 1465-3931</identifier><identifier>DOI: 10.1016/j.pathol.2019.12.003</identifier><identifier>PMID: 32113673</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Carcinoma, Squamous Cell - genetics ; EGFR mutation ; ErbB Receptors - genetics ; Female ; Humans ; Lung Neoplasms - genetics ; Male ; Middle Aged ; Mutation ; Non-small cell lung carcinoma ; Retrospective Studies ; squamous cell carcinoma</subject><ispartof>Pathology, 2020-04, Vol.52 (3), p.323-328</ispartof><rights>2020 Royal College of Pathologists of Australasia</rights><rights>Copyright © 2020 Royal College of Pathologists of Australasia. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-aa2b445cf7c8020117e2dd13e7390ba8ad754745ba49f84be9ebee71003fd9453</citedby><cites>FETCH-LOGICAL-c362t-aa2b445cf7c8020117e2dd13e7390ba8ad754745ba49f84be9ebee71003fd9453</cites><orcidid>0000-0002-8074-0900</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32113673$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheung, Alvin Ho-Kwan</creatorcontrib><creatorcontrib>Tong, Joanna Hung-Man</creatorcontrib><creatorcontrib>Chung, Lau-Ying</creatorcontrib><creatorcontrib>Chau, Shuk-Ling</creatorcontrib><creatorcontrib>Ng, Calvin Sze-Hang</creatorcontrib><creatorcontrib>Wan, Innes Y.P.</creatorcontrib><creatorcontrib>To, Ka-Fai</creatorcontrib><title>EGFR mutation exists in squamous cell lung carcinoma</title><title>Pathology</title><addtitle>Pathology</addtitle><description>Whether EGFR mutation occurs in lung squamous cell carcinoma (SCC) remains a controversial issue. Although numerous trials have shown positive response to tyrosine kinase inhibitors in SCC, these observations have not been well correlated with presence or absence of EGFR mutation. A complicating issue is that adenosquamous carcinoma, a mimic of SCC, frequently harbours EGFR mutations. We evaluated the EGFR mutation status of 191 cases initially diagnosed as SCC of lung origin in years 2000–2011, and performed a panel of markers including p40, p63, CK5/6, TTF-1, mucicarmine on the tissue microarray or tissue blocks from each case, to ascertain the squamous differentiation of each case. Four cases were found to have EGFR mutations, with three showing typical squamous morphological features and immunohistochemical profile on all available tumour blocks, and one reclassified as adenosquamous carcinoma. Mixed responses were noted for two of the patients with EGFR-mutated SCC treated with tyrosine kinase inhibitors. In conclusion, we report that a small subset of rigorously proven SCC harbours EGFR mutation. It also appears in our cohort that EGFR-mutated tumours, in the context of SCC, may have relatively poor response to tyrosine kinase inhibitors.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>EGFR mutation</subject><subject>ErbB Receptors - genetics</subject><subject>Female</subject><subject>Humans</subject><subject>Lung Neoplasms - genetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Non-small cell lung carcinoma</subject><subject>Retrospective Studies</subject><subject>squamous cell carcinoma</subject><issn>0031-3025</issn><issn>1465-3931</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLw0AUhQdRbK3-A5Es3STOK5nJRpDSVqEgiK6HyeRGp-TRziSi_94JqS5dXbicc893D0LXBCcEk-xul-x1_9HVCcUkTwhNMGYnaE54lsYsZ-QUzcOGxAzTdIYuvN9hjLmU8hzNGCWEZYLNEV9t1i9RM_S6t10bwZf1vY9sG_nDoJtu8JGBuo7qoX2PjHbGtl2jL9FZpWsPV8e5QG_r1evyMd4-b56WD9vYsIz2sda04Dw1lTASB0oigJYlYSBYjgstdSlSLnhaaJ5XkheQQwEgSMCuypynbIFup7t71x0G8L1qrB95dAsBTVGW5VJiKUWQ8klqXOe9g0rtnW20-1YEq7EvtVNTX2rsSxGqQkyw3RwThqKB8s_0W1AQ3E8CCH9-WnDKGwutgdI6ML0qO_t_wg9gkHzB</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Cheung, Alvin Ho-Kwan</creator><creator>Tong, Joanna Hung-Man</creator><creator>Chung, Lau-Ying</creator><creator>Chau, Shuk-Ling</creator><creator>Ng, Calvin Sze-Hang</creator><creator>Wan, Innes Y.P.</creator><creator>To, Ka-Fai</creator><general>Elsevier B.V</general><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><orcidid>https://orcid.org/0000-0002-8074-0900</orcidid></search><sort><creationdate>202004</creationdate><title>EGFR mutation exists in squamous cell lung carcinoma</title><author>Cheung, Alvin Ho-Kwan ; Tong, Joanna Hung-Man ; Chung, Lau-Ying ; Chau, Shuk-Ling ; Ng, Calvin Sze-Hang ; Wan, Innes Y.P. ; To, Ka-Fai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-aa2b445cf7c8020117e2dd13e7390ba8ad754745ba49f84be9ebee71003fd9453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>EGFR mutation</topic><topic>ErbB Receptors - genetics</topic><topic>Female</topic><topic>Humans</topic><topic>Lung Neoplasms - genetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Non-small cell lung carcinoma</topic><topic>Retrospective Studies</topic><topic>squamous cell carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheung, Alvin Ho-Kwan</creatorcontrib><creatorcontrib>Tong, Joanna Hung-Man</creatorcontrib><creatorcontrib>Chung, Lau-Ying</creatorcontrib><creatorcontrib>Chau, Shuk-Ling</creatorcontrib><creatorcontrib>Ng, Calvin Sze-Hang</creatorcontrib><creatorcontrib>Wan, Innes Y.P.</creatorcontrib><creatorcontrib>To, Ka-Fai</creatorcontrib><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>Pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheung, Alvin Ho-Kwan</au><au>Tong, Joanna Hung-Man</au><au>Chung, Lau-Ying</au><au>Chau, Shuk-Ling</au><au>Ng, Calvin Sze-Hang</au><au>Wan, Innes Y.P.</au><au>To, Ka-Fai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EGFR mutation exists in squamous cell lung carcinoma</atitle><jtitle>Pathology</jtitle><addtitle>Pathology</addtitle><date>2020-04</date><risdate>2020</risdate><volume>52</volume><issue>3</issue><spage>323</spage><epage>328</epage><pages>323-328</pages><issn>0031-3025</issn><eissn>1465-3931</eissn><abstract>Whether EGFR mutation occurs in lung squamous cell carcinoma (SCC) remains a controversial issue. Although numerous trials have shown positive response to tyrosine kinase inhibitors in SCC, these observations have not been well correlated with presence or absence of EGFR mutation. A complicating issue is that adenosquamous carcinoma, a mimic of SCC, frequently harbours EGFR mutations. We evaluated the EGFR mutation status of 191 cases initially diagnosed as SCC of lung origin in years 2000–2011, and performed a panel of markers including p40, p63, CK5/6, TTF-1, mucicarmine on the tissue microarray or tissue blocks from each case, to ascertain the squamous differentiation of each case. Four cases were found to have EGFR mutations, with three showing typical squamous morphological features and immunohistochemical profile on all available tumour blocks, and one reclassified as adenosquamous carcinoma. Mixed responses were noted for two of the patients with EGFR-mutated SCC treated with tyrosine kinase inhibitors. In conclusion, we report that a small subset of rigorously proven SCC harbours EGFR mutation. It also appears in our cohort that EGFR-mutated tumours, in the context of SCC, may have relatively poor response to tyrosine kinase inhibitors.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>32113673</pmid><doi>10.1016/j.pathol.2019.12.003</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-8074-0900</orcidid></addata></record> |
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subjects | Adult Aged Aged, 80 and over Carcinoma, Squamous Cell - genetics EGFR mutation ErbB Receptors - genetics Female Humans Lung Neoplasms - genetics Male Middle Aged Mutation Non-small cell lung carcinoma Retrospective Studies squamous cell carcinoma |
title | EGFR mutation exists in squamous cell lung carcinoma |
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