Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: The influence of age, grade, and histological type
BRCA1-related breast cancers are more frequently estrogen receptor (ER) negative than are either BRCA2-related or nonhereditary breast cancers. The relationship between ER status and other clinical features of hereditary breast cancers has not been well studied. ER status, grade, and histological tu...
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Veröffentlicht in: | Clinical cancer research 2004-03, Vol.10 (6), p.2029-2034 |
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creator | FOULKES, William D METCALFE, Kelly OLIVOTTO, Ivo A BEGIN, Louis R NAROD, Steven A PING SUN HANNA, Wedad M LYNCH, Henry T GHADIRIAN, Parviz TUNG, Nadine OLOPADE, Olufunmilayo I WEBER, Barbara L MCLENNAN, Jane |
description | BRCA1-related breast cancers are more frequently estrogen receptor (ER) negative than are either BRCA2-related or nonhereditary breast cancers. The relationship between ER status and other clinical features of hereditary breast cancers has not been well studied.
ER status, grade, and histological tumor type were evaluated in 1131 women with invasive breast cancer, ascertained at 10 centers in North America. There were 208 BRCA1 mutation carriers, 88 BRCA2 carriers, and 804 women without a known mutation. We stratified the patients by mutation status, grade, age, and histological type and calculated the percentage of ER-positive tumors within each stratum.
BRCA1 mutation carriers were more likely to have ER-negative breast cancers than were women in other groups, after adjustment for age, grade, and histological subtype (P < 0.001). Only 3.9% of BRCA1-related breast cancers were ER-positive cancers occurring in women in their postmenopausal years. The direction and magnitude of the change in ER status with increasing age at diagnosis in BRCA1 carriers was significantly different from in BRCA2 carriers (P(intercept) = 0.0002, P(slope) = 0.04). Notably, changes in ER status with age at diagnosis for BRCA1 carriers and noncarriers were almost identical (P(slope) = 0.98).
The strong relationship between the presence of a BRCA1 mutation and the ER-negative status of the breast cancers is neither a consequence of the young age at onset nor the high grade but is an intrinsic property of BRCA1-related cancers. The ER-negative status of these cancers may reflect the cell of origin of BRCA1-related cancers. |
doi_str_mv | 10.1158/1078-0432.CCR-03-1061 |
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ER status, grade, and histological tumor type were evaluated in 1131 women with invasive breast cancer, ascertained at 10 centers in North America. There were 208 BRCA1 mutation carriers, 88 BRCA2 carriers, and 804 women without a known mutation. We stratified the patients by mutation status, grade, age, and histological type and calculated the percentage of ER-positive tumors within each stratum.
BRCA1 mutation carriers were more likely to have ER-negative breast cancers than were women in other groups, after adjustment for age, grade, and histological subtype (P < 0.001). Only 3.9% of BRCA1-related breast cancers were ER-positive cancers occurring in women in their postmenopausal years. The direction and magnitude of the change in ER status with increasing age at diagnosis in BRCA1 carriers was significantly different from in BRCA2 carriers (P(intercept) = 0.0002, P(slope) = 0.04). Notably, changes in ER status with age at diagnosis for BRCA1 carriers and noncarriers were almost identical (P(slope) = 0.98).
The strong relationship between the presence of a BRCA1 mutation and the ER-negative status of the breast cancers is neither a consequence of the young age at onset nor the high grade but is an intrinsic property of BRCA1-related cancers. The ER-negative status of these cancers may reflect the cell of origin of BRCA1-related cancers.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-03-1061</identifier><identifier>PMID: 15041722</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adult ; Age Factors ; Age of Onset ; Aged ; Aged, 80 and over ; Antineoplastic agents ; Biological and medical sciences ; BRCA1 Protein - genetics ; BRCA2 Protein - genetics ; Breast Neoplasms - classification ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Female ; Genetic Carrier Screening ; Humans ; Medical sciences ; Middle Aged ; Mutation - genetics ; Pharmacology. Drug treatments ; Receptors, Estrogen - analysis ; Tumors</subject><ispartof>Clinical cancer research, 2004-03, Vol.10 (6), p.2029-2034</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c291t-3e386d0318d97f27105baa5d886a92052a513ab3dca84513f715e6442753e8d43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15581786$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15041722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FOULKES, William D</creatorcontrib><creatorcontrib>METCALFE, Kelly</creatorcontrib><creatorcontrib>OLIVOTTO, Ivo A</creatorcontrib><creatorcontrib>BEGIN, Louis R</creatorcontrib><creatorcontrib>NAROD, Steven A</creatorcontrib><creatorcontrib>PING SUN</creatorcontrib><creatorcontrib>HANNA, Wedad M</creatorcontrib><creatorcontrib>LYNCH, Henry T</creatorcontrib><creatorcontrib>GHADIRIAN, Parviz</creatorcontrib><creatorcontrib>TUNG, Nadine</creatorcontrib><creatorcontrib>OLOPADE, Olufunmilayo I</creatorcontrib><creatorcontrib>WEBER, Barbara L</creatorcontrib><creatorcontrib>MCLENNAN, Jane</creatorcontrib><title>Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: The influence of age, grade, and histological type</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>BRCA1-related breast cancers are more frequently estrogen receptor (ER) negative than are either BRCA2-related or nonhereditary breast cancers. The relationship between ER status and other clinical features of hereditary breast cancers has not been well studied.
ER status, grade, and histological tumor type were evaluated in 1131 women with invasive breast cancer, ascertained at 10 centers in North America. There were 208 BRCA1 mutation carriers, 88 BRCA2 carriers, and 804 women without a known mutation. We stratified the patients by mutation status, grade, age, and histological type and calculated the percentage of ER-positive tumors within each stratum.
BRCA1 mutation carriers were more likely to have ER-negative breast cancers than were women in other groups, after adjustment for age, grade, and histological subtype (P < 0.001). Only 3.9% of BRCA1-related breast cancers were ER-positive cancers occurring in women in their postmenopausal years. The direction and magnitude of the change in ER status with increasing age at diagnosis in BRCA1 carriers was significantly different from in BRCA2 carriers (P(intercept) = 0.0002, P(slope) = 0.04). Notably, changes in ER status with age at diagnosis for BRCA1 carriers and noncarriers were almost identical (P(slope) = 0.98).
The strong relationship between the presence of a BRCA1 mutation and the ER-negative status of the breast cancers is neither a consequence of the young age at onset nor the high grade but is an intrinsic property of BRCA1-related cancers. The ER-negative status of these cancers may reflect the cell of origin of BRCA1-related cancers.</description><subject>Adult</subject><subject>Age Factors</subject><subject>Age of Onset</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>BRCA1 Protein - genetics</subject><subject>BRCA2 Protein - genetics</subject><subject>Breast Neoplasms - classification</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Female</subject><subject>Genetic Carrier Screening</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mutation - genetics</subject><subject>Pharmacology. Drug treatments</subject><subject>Receptors, Estrogen - analysis</subject><subject>Tumors</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1LxDAQhoMofv8EJRc9Gc0kTZP1tha_QBBEz8tsM10r3XZNUsF_b9QVPL3PwDMD7zB2BPIcwLgLkNYJWWh1XlVPQmoBsoQNtgvGWKFVaTYz_zk7bC_GNymhAFlssx0wsgCr1C77uI4pDAvqeaCaVmkIPCZMY-Rtz6-eqikIjr3_QSUCdZjI83kgjInX2NcULvnzK2W96UbKMx8ajgs644uAPsf39msb09ANi7bGjqfPFR2wrQa7SIfr3GcvN9fP1Z14eLy9r6YPolYTSEKTdqWXGpyf2EZZkGaOaLxzJU6UNAoNaJxrX6MrMjYWDJVFoazR5Hyh99np791VGN5Himm2bGNNXYc9DWOcWbDGalNm8XgtjvMl-dkqtEsMn7O_T2XhZC1gzC2akLu38Z9nHFhX6i_NyHah</recordid><startdate>20040315</startdate><enddate>20040315</enddate><creator>FOULKES, William D</creator><creator>METCALFE, Kelly</creator><creator>OLIVOTTO, Ivo A</creator><creator>BEGIN, Louis R</creator><creator>NAROD, Steven A</creator><creator>PING SUN</creator><creator>HANNA, Wedad M</creator><creator>LYNCH, Henry T</creator><creator>GHADIRIAN, Parviz</creator><creator>TUNG, Nadine</creator><creator>OLOPADE, Olufunmilayo I</creator><creator>WEBER, Barbara L</creator><creator>MCLENNAN, Jane</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20040315</creationdate><title>Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: The influence of age, grade, and histological type</title><author>FOULKES, William D ; METCALFE, Kelly ; OLIVOTTO, Ivo A ; BEGIN, Louis R ; NAROD, Steven A ; PING SUN ; HANNA, Wedad M ; LYNCH, Henry T ; GHADIRIAN, Parviz ; TUNG, Nadine ; OLOPADE, Olufunmilayo I ; WEBER, Barbara L ; MCLENNAN, Jane</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c291t-3e386d0318d97f27105baa5d886a92052a513ab3dca84513f715e6442753e8d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Age of Onset</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>BRCA1 Protein - genetics</topic><topic>BRCA2 Protein - genetics</topic><topic>Breast Neoplasms - classification</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Female</topic><topic>Genetic Carrier Screening</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mutation - genetics</topic><topic>Pharmacology. Drug treatments</topic><topic>Receptors, Estrogen - analysis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FOULKES, William D</creatorcontrib><creatorcontrib>METCALFE, Kelly</creatorcontrib><creatorcontrib>OLIVOTTO, Ivo A</creatorcontrib><creatorcontrib>BEGIN, Louis R</creatorcontrib><creatorcontrib>NAROD, Steven A</creatorcontrib><creatorcontrib>PING SUN</creatorcontrib><creatorcontrib>HANNA, Wedad M</creatorcontrib><creatorcontrib>LYNCH, Henry T</creatorcontrib><creatorcontrib>GHADIRIAN, Parviz</creatorcontrib><creatorcontrib>TUNG, Nadine</creatorcontrib><creatorcontrib>OLOPADE, Olufunmilayo I</creatorcontrib><creatorcontrib>WEBER, Barbara L</creatorcontrib><creatorcontrib>MCLENNAN, Jane</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>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FOULKES, William D</au><au>METCALFE, Kelly</au><au>OLIVOTTO, Ivo A</au><au>BEGIN, Louis R</au><au>NAROD, Steven A</au><au>PING SUN</au><au>HANNA, Wedad M</au><au>LYNCH, Henry T</au><au>GHADIRIAN, Parviz</au><au>TUNG, Nadine</au><au>OLOPADE, Olufunmilayo I</au><au>WEBER, Barbara L</au><au>MCLENNAN, Jane</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: The influence of age, grade, and histological type</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2004-03-15</date><risdate>2004</risdate><volume>10</volume><issue>6</issue><spage>2029</spage><epage>2034</epage><pages>2029-2034</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>BRCA1-related breast cancers are more frequently estrogen receptor (ER) negative than are either BRCA2-related or nonhereditary breast cancers. The relationship between ER status and other clinical features of hereditary breast cancers has not been well studied.
ER status, grade, and histological tumor type were evaluated in 1131 women with invasive breast cancer, ascertained at 10 centers in North America. There were 208 BRCA1 mutation carriers, 88 BRCA2 carriers, and 804 women without a known mutation. We stratified the patients by mutation status, grade, age, and histological type and calculated the percentage of ER-positive tumors within each stratum.
BRCA1 mutation carriers were more likely to have ER-negative breast cancers than were women in other groups, after adjustment for age, grade, and histological subtype (P < 0.001). Only 3.9% of BRCA1-related breast cancers were ER-positive cancers occurring in women in their postmenopausal years. The direction and magnitude of the change in ER status with increasing age at diagnosis in BRCA1 carriers was significantly different from in BRCA2 carriers (P(intercept) = 0.0002, P(slope) = 0.04). Notably, changes in ER status with age at diagnosis for BRCA1 carriers and noncarriers were almost identical (P(slope) = 0.98).
The strong relationship between the presence of a BRCA1 mutation and the ER-negative status of the breast cancers is neither a consequence of the young age at onset nor the high grade but is an intrinsic property of BRCA1-related cancers. The ER-negative status of these cancers may reflect the cell of origin of BRCA1-related cancers.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>15041722</pmid><doi>10.1158/1078-0432.CCR-03-1061</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Age Factors Age of Onset Aged Aged, 80 and over Antineoplastic agents Biological and medical sciences BRCA1 Protein - genetics BRCA2 Protein - genetics Breast Neoplasms - classification Breast Neoplasms - genetics Breast Neoplasms - pathology Female Genetic Carrier Screening Humans Medical sciences Middle Aged Mutation - genetics Pharmacology. Drug treatments Receptors, Estrogen - analysis Tumors |
title | Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: The influence of age, grade, and histological type |
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