Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype
Purpose: To investigate the proportion of breast cancers arising in patients with germ line BRCA1 and BRCA2 mutations expressing basal markers and developing predictive tests for identification of high-risk patients. Experimental Design: Histopathologic material from 182 tumors in BRCA1 mutation car...
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creator | Lakhani, Sunil R Reis-Filho, Jorge S Fulford, Laura Penault-Llorca, Frederique van der Vijver, Marc Parry, Suzanne Bishop, Timothy Benitez, Javier Rivas, Carmen Bignon, Yves-Jean Chang-Claude, Jenny Hamann, Ute Cornelisse, Cees J Devilee, Peter Beckmann, Matthias W Nestle-Krämling, Carolin Daly, Peter A Haites, Neva Varley, Jenny Lalloo, Fiona Evans, Gareth Maugard, Christine Meijers-Heijboer, Hanne Klijn, Jan G M Olah, Edith Gusterson, Barry A Pilotti, Silvana Radice, Paolo Scherneck, Siegfried Sobol, Hagay Jacquemier, Jocelyne Wagner, Teresa Peto, Julian Stratton, Michael R McGuffog, Lesley Easton, Douglas F |
description | Purpose: To investigate the proportion of breast cancers arising in patients with germ line BRCA1 and BRCA2 mutations expressing basal markers and developing predictive tests for identification of high-risk patients.
Experimental Design: Histopathologic material from 182 tumors in BRCA1 mutation carriers, 63 BRCA2 carriers, and 109 controls, collected as part of the international Breast Cancer Linkage Consortium were immunohistochemically
stained for CK14, CK5/6, CK17, epidermal growth factor receptor (EGFR), and osteonectin.
Results: All five basal markers were commoner in BRCA1 tumors than in control tumors (CK14: 61% versus 12%; CK5/6: 58% versus 7%; CK17: 53% versus 10%; osteonectin: 43% versus
19%; EGFR: 67% versus 21%; P < 0.0001 in each case). In a multivariate analysis, CK14, CK5/6, and estrogen receptor (ER) remained significant predictors
of BRCA1 carrier status. In contrast, the frequency of basal markers in BRCA2 tumors did not differ significant from controls.
Conclusion: The use of cytokeratin staining in combination with ER and morphology provides a more accurate predictor of BRCA1 mutation status than previously available, that may be useful in selecting patients for BRCA1 mutation testing. The high percentage of BRCA1 cases positive for EGFR suggests that specific anti-tyrosine kinase therapy may be of potential benefit in these patients. |
doi_str_mv | 10.1158/1078-0432.CCR-04-2424 |
format | Article |
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Experimental Design: Histopathologic material from 182 tumors in BRCA1 mutation carriers, 63 BRCA2 carriers, and 109 controls, collected as part of the international Breast Cancer Linkage Consortium were immunohistochemically
stained for CK14, CK5/6, CK17, epidermal growth factor receptor (EGFR), and osteonectin.
Results: All five basal markers were commoner in BRCA1 tumors than in control tumors (CK14: 61% versus 12%; CK5/6: 58% versus 7%; CK17: 53% versus 10%; osteonectin: 43% versus
19%; EGFR: 67% versus 21%; P < 0.0001 in each case). In a multivariate analysis, CK14, CK5/6, and estrogen receptor (ER) remained significant predictors
of BRCA1 carrier status. In contrast, the frequency of basal markers in BRCA2 tumors did not differ significant from controls.
Conclusion: The use of cytokeratin staining in combination with ER and morphology provides a more accurate predictor of BRCA1 mutation status than previously available, that may be useful in selecting patients for BRCA1 mutation testing. The high percentage of BRCA1 cases positive for EGFR suggests that specific anti-tyrosine kinase therapy may be of potential benefit in these patients.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-04-2424</identifier><identifier>PMID: 16033833</identifier><language>eng</language><publisher>United States: American Association for Cancer Research</publisher><subject>Basal ; Biomarkers, Tumor - analysis ; BRCA1 ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Case-Control Studies ; DNA Mutational Analysis ; Female ; Genes, BRCA1 ; Genes, BRCA2 ; Germ-Line Mutation ; Humans ; Immunohistochemistry ; immunophenotype ; Keratins ; Middle Aged ; Multivariate Analysis ; myoepithelial ; Phenotype ; Prognosis ; Receptors, Estrogen - analysis ; Risk Assessment ; Sensitivity and Specificity</subject><ispartof>Clinical cancer research, 2005-07, Vol.11 (14), p.5175-5180</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-a7c42f7dac9f8fc0946f9eb2c3c5be9b369c612928f72a5d96cbdef249d061263</citedby><cites>FETCH-LOGICAL-c419t-a7c42f7dac9f8fc0946f9eb2c3c5be9b369c612928f72a5d96cbdef249d061263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3343,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16033833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lakhani, Sunil R</creatorcontrib><creatorcontrib>Reis-Filho, Jorge S</creatorcontrib><creatorcontrib>Fulford, Laura</creatorcontrib><creatorcontrib>Penault-Llorca, Frederique</creatorcontrib><creatorcontrib>van der Vijver, Marc</creatorcontrib><creatorcontrib>Parry, Suzanne</creatorcontrib><creatorcontrib>Bishop, Timothy</creatorcontrib><creatorcontrib>Benitez, Javier</creatorcontrib><creatorcontrib>Rivas, Carmen</creatorcontrib><creatorcontrib>Bignon, Yves-Jean</creatorcontrib><creatorcontrib>Chang-Claude, Jenny</creatorcontrib><creatorcontrib>Hamann, Ute</creatorcontrib><creatorcontrib>Cornelisse, Cees J</creatorcontrib><creatorcontrib>Devilee, Peter</creatorcontrib><creatorcontrib>Beckmann, Matthias W</creatorcontrib><creatorcontrib>Nestle-Krämling, Carolin</creatorcontrib><creatorcontrib>Daly, Peter A</creatorcontrib><creatorcontrib>Haites, Neva</creatorcontrib><creatorcontrib>Varley, Jenny</creatorcontrib><creatorcontrib>Lalloo, Fiona</creatorcontrib><creatorcontrib>Evans, Gareth</creatorcontrib><creatorcontrib>Maugard, Christine</creatorcontrib><creatorcontrib>Meijers-Heijboer, Hanne</creatorcontrib><creatorcontrib>Klijn, Jan G M</creatorcontrib><creatorcontrib>Olah, Edith</creatorcontrib><creatorcontrib>Gusterson, Barry A</creatorcontrib><creatorcontrib>Pilotti, Silvana</creatorcontrib><creatorcontrib>Radice, Paolo</creatorcontrib><creatorcontrib>Scherneck, Siegfried</creatorcontrib><creatorcontrib>Sobol, Hagay</creatorcontrib><creatorcontrib>Jacquemier, Jocelyne</creatorcontrib><creatorcontrib>Wagner, Teresa</creatorcontrib><creatorcontrib>Peto, Julian</creatorcontrib><creatorcontrib>Stratton, Michael R</creatorcontrib><creatorcontrib>McGuffog, Lesley</creatorcontrib><creatorcontrib>Easton, Douglas F</creatorcontrib><creatorcontrib>Breast Cancer Linkage Consortium</creatorcontrib><creatorcontrib>the Breast Cancer Linkage Consortium</creatorcontrib><title>Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Purpose: To investigate the proportion of breast cancers arising in patients with germ line BRCA1 and BRCA2 mutations expressing basal markers and developing predictive tests for identification of high-risk patients.
Experimental Design: Histopathologic material from 182 tumors in BRCA1 mutation carriers, 63 BRCA2 carriers, and 109 controls, collected as part of the international Breast Cancer Linkage Consortium were immunohistochemically
stained for CK14, CK5/6, CK17, epidermal growth factor receptor (EGFR), and osteonectin.
Results: All five basal markers were commoner in BRCA1 tumors than in control tumors (CK14: 61% versus 12%; CK5/6: 58% versus 7%; CK17: 53% versus 10%; osteonectin: 43% versus
19%; EGFR: 67% versus 21%; P < 0.0001 in each case). In a multivariate analysis, CK14, CK5/6, and estrogen receptor (ER) remained significant predictors
of BRCA1 carrier status. In contrast, the frequency of basal markers in BRCA2 tumors did not differ significant from controls.
Conclusion: The use of cytokeratin staining in combination with ER and morphology provides a more accurate predictor of BRCA1 mutation status than previously available, that may be useful in selecting patients for BRCA1 mutation testing. The high percentage of BRCA1 cases positive for EGFR suggests that specific anti-tyrosine kinase therapy may be of potential benefit in these patients.</description><subject>Basal</subject><subject>Biomarkers, Tumor - analysis</subject><subject>BRCA1</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Case-Control Studies</subject><subject>DNA Mutational Analysis</subject><subject>Female</subject><subject>Genes, BRCA1</subject><subject>Genes, BRCA2</subject><subject>Germ-Line Mutation</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>immunophenotype</subject><subject>Keratins</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>myoepithelial</subject><subject>Phenotype</subject><subject>Prognosis</subject><subject>Receptors, Estrogen - analysis</subject><subject>Risk Assessment</subject><subject>Sensitivity and Specificity</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtrGzEUhUVpaV79CS1aFbqYRO8ZLeMhbQqBGDdZC43myqNia1xJJuTfV65duuzqHi7fuRfOQegjJdeUyu6GkrZriODsuu9XVTRMMPEGnVMp24YzJd9W_Zc5Qxc5_ySECkrEe3RGFeG84_wcwTLBGFwJc8Szx4tVf0vxj2LLPuMQ8dKWALFk_BLKhBcJbC64t9FBws85xDW-yyXNa4h4BQ52ZU7YxhEvbLYbvJwgzuV1B1fonbebDB9O8xI9f7176u-bh8dv3_vbh8YJqktjWyeYb0frtO-8I1oor2Fgjjs5gB640k5RplnnW2blqJUbRvBM6JHUveKX6PPx7i7Nv_aQi9mG7GCzsRHmfTaqI1J1WvwXpC3vlJaygvIIujTnnMCbXQpbm14NJeZQhDmEbA4hm1pEFeZQRPV9Oj3YD1sY_7lOyVfgyxGYwnp6CQmM-xNrggw2uakeN1QYSVvJfwPBapIl</recordid><startdate>20050715</startdate><enddate>20050715</enddate><creator>Lakhani, Sunil R</creator><creator>Reis-Filho, Jorge S</creator><creator>Fulford, Laura</creator><creator>Penault-Llorca, Frederique</creator><creator>van der Vijver, Marc</creator><creator>Parry, Suzanne</creator><creator>Bishop, Timothy</creator><creator>Benitez, Javier</creator><creator>Rivas, Carmen</creator><creator>Bignon, Yves-Jean</creator><creator>Chang-Claude, Jenny</creator><creator>Hamann, Ute</creator><creator>Cornelisse, Cees J</creator><creator>Devilee, Peter</creator><creator>Beckmann, Matthias W</creator><creator>Nestle-Krämling, Carolin</creator><creator>Daly, Peter A</creator><creator>Haites, Neva</creator><creator>Varley, Jenny</creator><creator>Lalloo, Fiona</creator><creator>Evans, Gareth</creator><creator>Maugard, Christine</creator><creator>Meijers-Heijboer, Hanne</creator><creator>Klijn, Jan G M</creator><creator>Olah, Edith</creator><creator>Gusterson, Barry A</creator><creator>Pilotti, Silvana</creator><creator>Radice, Paolo</creator><creator>Scherneck, Siegfried</creator><creator>Sobol, Hagay</creator><creator>Jacquemier, Jocelyne</creator><creator>Wagner, Teresa</creator><creator>Peto, Julian</creator><creator>Stratton, Michael R</creator><creator>McGuffog, Lesley</creator><creator>Easton, Douglas F</creator><general>American Association for Cancer Research</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>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20050715</creationdate><title>Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype</title><author>Lakhani, Sunil R ; Reis-Filho, Jorge S ; Fulford, Laura ; Penault-Llorca, Frederique ; van der Vijver, Marc ; Parry, Suzanne ; Bishop, Timothy ; Benitez, Javier ; Rivas, Carmen ; Bignon, Yves-Jean ; Chang-Claude, Jenny ; Hamann, Ute ; Cornelisse, Cees J ; Devilee, Peter ; Beckmann, Matthias W ; Nestle-Krämling, Carolin ; Daly, Peter A ; Haites, Neva ; Varley, Jenny ; Lalloo, Fiona ; Evans, Gareth ; Maugard, Christine ; Meijers-Heijboer, Hanne ; Klijn, Jan G M ; Olah, Edith ; Gusterson, Barry A ; Pilotti, Silvana ; Radice, Paolo ; Scherneck, Siegfried ; Sobol, Hagay ; Jacquemier, Jocelyne ; Wagner, Teresa ; Peto, Julian ; Stratton, Michael R ; McGuffog, Lesley ; Easton, Douglas F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-a7c42f7dac9f8fc0946f9eb2c3c5be9b369c612928f72a5d96cbdef249d061263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Basal</topic><topic>Biomarkers, Tumor - analysis</topic><topic>BRCA1</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Case-Control Studies</topic><topic>DNA Mutational Analysis</topic><topic>Female</topic><topic>Genes, BRCA1</topic><topic>Genes, BRCA2</topic><topic>Germ-Line Mutation</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>immunophenotype</topic><topic>Keratins</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>myoepithelial</topic><topic>Phenotype</topic><topic>Prognosis</topic><topic>Receptors, Estrogen - analysis</topic><topic>Risk Assessment</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lakhani, Sunil R</creatorcontrib><creatorcontrib>Reis-Filho, Jorge S</creatorcontrib><creatorcontrib>Fulford, Laura</creatorcontrib><creatorcontrib>Penault-Llorca, Frederique</creatorcontrib><creatorcontrib>van der Vijver, Marc</creatorcontrib><creatorcontrib>Parry, Suzanne</creatorcontrib><creatorcontrib>Bishop, Timothy</creatorcontrib><creatorcontrib>Benitez, Javier</creatorcontrib><creatorcontrib>Rivas, Carmen</creatorcontrib><creatorcontrib>Bignon, Yves-Jean</creatorcontrib><creatorcontrib>Chang-Claude, Jenny</creatorcontrib><creatorcontrib>Hamann, Ute</creatorcontrib><creatorcontrib>Cornelisse, Cees J</creatorcontrib><creatorcontrib>Devilee, Peter</creatorcontrib><creatorcontrib>Beckmann, Matthias W</creatorcontrib><creatorcontrib>Nestle-Krämling, Carolin</creatorcontrib><creatorcontrib>Daly, Peter A</creatorcontrib><creatorcontrib>Haites, Neva</creatorcontrib><creatorcontrib>Varley, Jenny</creatorcontrib><creatorcontrib>Lalloo, Fiona</creatorcontrib><creatorcontrib>Evans, Gareth</creatorcontrib><creatorcontrib>Maugard, Christine</creatorcontrib><creatorcontrib>Meijers-Heijboer, Hanne</creatorcontrib><creatorcontrib>Klijn, Jan G M</creatorcontrib><creatorcontrib>Olah, Edith</creatorcontrib><creatorcontrib>Gusterson, Barry A</creatorcontrib><creatorcontrib>Pilotti, Silvana</creatorcontrib><creatorcontrib>Radice, Paolo</creatorcontrib><creatorcontrib>Scherneck, Siegfried</creatorcontrib><creatorcontrib>Sobol, Hagay</creatorcontrib><creatorcontrib>Jacquemier, Jocelyne</creatorcontrib><creatorcontrib>Wagner, Teresa</creatorcontrib><creatorcontrib>Peto, Julian</creatorcontrib><creatorcontrib>Stratton, Michael R</creatorcontrib><creatorcontrib>McGuffog, Lesley</creatorcontrib><creatorcontrib>Easton, Douglas F</creatorcontrib><creatorcontrib>Breast Cancer Linkage Consortium</creatorcontrib><creatorcontrib>the Breast Cancer Linkage Consortium</creatorcontrib><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>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lakhani, Sunil R</au><au>Reis-Filho, Jorge S</au><au>Fulford, Laura</au><au>Penault-Llorca, Frederique</au><au>van der Vijver, Marc</au><au>Parry, Suzanne</au><au>Bishop, Timothy</au><au>Benitez, Javier</au><au>Rivas, Carmen</au><au>Bignon, Yves-Jean</au><au>Chang-Claude, Jenny</au><au>Hamann, Ute</au><au>Cornelisse, Cees J</au><au>Devilee, Peter</au><au>Beckmann, Matthias W</au><au>Nestle-Krämling, Carolin</au><au>Daly, Peter A</au><au>Haites, Neva</au><au>Varley, Jenny</au><au>Lalloo, Fiona</au><au>Evans, Gareth</au><au>Maugard, Christine</au><au>Meijers-Heijboer, Hanne</au><au>Klijn, Jan G M</au><au>Olah, Edith</au><au>Gusterson, Barry A</au><au>Pilotti, Silvana</au><au>Radice, Paolo</au><au>Scherneck, Siegfried</au><au>Sobol, Hagay</au><au>Jacquemier, Jocelyne</au><au>Wagner, Teresa</au><au>Peto, Julian</au><au>Stratton, Michael R</au><au>McGuffog, Lesley</au><au>Easton, Douglas F</au><aucorp>Breast Cancer Linkage Consortium</aucorp><aucorp>the Breast Cancer Linkage Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2005-07-15</date><risdate>2005</risdate><volume>11</volume><issue>14</issue><spage>5175</spage><epage>5180</epage><pages>5175-5180</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Purpose: To investigate the proportion of breast cancers arising in patients with germ line BRCA1 and BRCA2 mutations expressing basal markers and developing predictive tests for identification of high-risk patients.
Experimental Design: Histopathologic material from 182 tumors in BRCA1 mutation carriers, 63 BRCA2 carriers, and 109 controls, collected as part of the international Breast Cancer Linkage Consortium were immunohistochemically
stained for CK14, CK5/6, CK17, epidermal growth factor receptor (EGFR), and osteonectin.
Results: All five basal markers were commoner in BRCA1 tumors than in control tumors (CK14: 61% versus 12%; CK5/6: 58% versus 7%; CK17: 53% versus 10%; osteonectin: 43% versus
19%; EGFR: 67% versus 21%; P < 0.0001 in each case). In a multivariate analysis, CK14, CK5/6, and estrogen receptor (ER) remained significant predictors
of BRCA1 carrier status. In contrast, the frequency of basal markers in BRCA2 tumors did not differ significant from controls.
Conclusion: The use of cytokeratin staining in combination with ER and morphology provides a more accurate predictor of BRCA1 mutation status than previously available, that may be useful in selecting patients for BRCA1 mutation testing. The high percentage of BRCA1 cases positive for EGFR suggests that specific anti-tyrosine kinase therapy may be of potential benefit in these patients.</abstract><cop>United States</cop><pub>American Association for Cancer Research</pub><pmid>16033833</pmid><doi>10.1158/1078-0432.CCR-04-2424</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Basal Biomarkers, Tumor - analysis BRCA1 Breast Neoplasms - genetics Breast Neoplasms - pathology Case-Control Studies DNA Mutational Analysis Female Genes, BRCA1 Genes, BRCA2 Germ-Line Mutation Humans Immunohistochemistry immunophenotype Keratins Middle Aged Multivariate Analysis myoepithelial Phenotype Prognosis Receptors, Estrogen - analysis Risk Assessment Sensitivity and Specificity |
title | Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype |
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