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Two histopathologically different diseases: hormone receptor-positive and hormone receptor-negative tumors in HER2-positive breast cancer
The clinical behavior of human epidermal growth factor 2 (HER2)-positive breast cancer, including pathologic complete response rate and pattern of relapse and metastasis, differs substantially according to hormone receptor (HR) status. We investigated various histopathologic features of HER2-positiv...
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Published in: | Breast cancer research and treatment 2014-06, Vol.145 (3), p.615-623 |
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container_title | Breast cancer research and treatment |
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creator | Lee, Hee Jin Park, In Ah Park, So Yeon Seo, An Na Lim, Bora Chai, Yun Song, In Hye Kim, Na Eun Kim, Joo Young Yu, Jong Han Ahn, Jin-Hee Gong, Gyungyub |
description | The clinical behavior of human epidermal growth factor 2 (HER2)-positive breast cancer, including pathologic complete response rate and pattern of relapse and metastasis, differs substantially according to hormone receptor (HR) status. We investigated various histopathologic features of HER2-positive breast cancer and their correlation with HR status. We retrospectively analyzed tumors of 450 HER2-positive breast cancer patients treated with chemotherapy and 1 year of trastuzumab. HR−/HER2+ tumors showed higher nuclear grade, less tubule formation, higher histologic grade, frequent apocrine features, diffuse and abundant lymphocytic infiltration, strong HER2 immunohistochemical staining (3+), higher average
HER2
copy number and
HER2
/
CEP17
ratio, the absence of
HER2
genetic heterogeneity, and greater p53 expression than HR+/HER2+ tumors. An inverse correlation was observed between estrogen receptor or progesterone receptor Allred score and average
HER2
copy number or
HER2
/
CEP17
ratio. The percentage of ductal carcinoma in situ (DCIS) within the tumor was negatively correlated with ER Allred score, but positively correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. Pathologic tumor size and DCIS percentage also showed a significant inverse correlation. Ratio of metastatic to total examined lymph node number was significantly correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. High pT stage (hazard ratio, 2.370;
p
= 0.027), the presence of lymphovascular invasion (hazard ratio, 2.806;
p
= 0.005), and HR negativity (hazard ratio, 2.202; 1.074–4.513;
p
= 0.031) were found to be independent prognostic indicators of poor disease-free survival. In conclusion, HR+/HER2+ and HR−/HER2+ breast cancer showed distinct histopathologic features that may be relevant to their distinct clinical behavior. |
doi_str_mv | 10.1007/s10549-014-2983-x |
format | article |
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HER2
copy number and
HER2
/
CEP17
ratio, the absence of
HER2
genetic heterogeneity, and greater p53 expression than HR+/HER2+ tumors. An inverse correlation was observed between estrogen receptor or progesterone receptor Allred score and average
HER2
copy number or
HER2
/
CEP17
ratio. The percentage of ductal carcinoma in situ (DCIS) within the tumor was negatively correlated with ER Allred score, but positively correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. Pathologic tumor size and DCIS percentage also showed a significant inverse correlation. Ratio of metastatic to total examined lymph node number was significantly correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. High pT stage (hazard ratio, 2.370;
p
= 0.027), the presence of lymphovascular invasion (hazard ratio, 2.806;
p
= 0.005), and HR negativity (hazard ratio, 2.202; 1.074–4.513;
p
= 0.031) were found to be independent prognostic indicators of poor disease-free survival. In conclusion, HR+/HER2+ and HR−/HER2+ breast cancer showed distinct histopathologic features that may be relevant to their distinct clinical behavior.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-014-2983-x</identifier><identifier>PMID: 24820412</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Adult ; Aged ; Analysis ; Antibodies, Monoclonal, Humanized - therapeutic use ; Antineoplastic Agents - therapeutic use ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; Cancer ; Cancer research ; Cancer therapies ; Carcinoma, Intraductal, Noninfiltrating ; Care and treatment ; Chemotherapy ; Disease-Free Survival ; Epidermal growth factor ; Female ; Gene Amplification ; Histopathology ; Hormones ; Hormones, Sex ; Humans ; Immunohistochemistry ; Medicine ; Medicine & Public Health ; Middle Aged ; Neoplasm Grading ; Oncology ; Preclinical Study ; Receptor, ErbB-2 - biosynthesis ; Receptor, ErbB-2 - genetics ; Receptors, Estrogen - metabolism ; Receptors, Progesterone - metabolism ; Retrospective Studies ; Trastuzumab ; Tumor proteins ; Tumor Suppressor Protein p53 - biosynthesis ; Young Adult</subject><ispartof>Breast cancer research and treatment, 2014-06, Vol.145 (3), p.615-623</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>COPYRIGHT 2014 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c606t-bcbb6c32c3593548563dd64853b5660b82d1766a0f15c6ae5344215036ca68823</citedby><cites>FETCH-LOGICAL-c606t-bcbb6c32c3593548563dd64853b5660b82d1766a0f15c6ae5344215036ca68823</cites></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/24820412$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Hee Jin</creatorcontrib><creatorcontrib>Park, In Ah</creatorcontrib><creatorcontrib>Park, So Yeon</creatorcontrib><creatorcontrib>Seo, An Na</creatorcontrib><creatorcontrib>Lim, Bora</creatorcontrib><creatorcontrib>Chai, Yun</creatorcontrib><creatorcontrib>Song, In Hye</creatorcontrib><creatorcontrib>Kim, Na Eun</creatorcontrib><creatorcontrib>Kim, Joo Young</creatorcontrib><creatorcontrib>Yu, Jong Han</creatorcontrib><creatorcontrib>Ahn, Jin-Hee</creatorcontrib><creatorcontrib>Gong, Gyungyub</creatorcontrib><title>Two histopathologically different diseases: hormone receptor-positive and hormone receptor-negative tumors in HER2-positive breast cancer</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>The clinical behavior of human epidermal growth factor 2 (HER2)-positive breast cancer, including pathologic complete response rate and pattern of relapse and metastasis, differs substantially according to hormone receptor (HR) status. We investigated various histopathologic features of HER2-positive breast cancer and their correlation with HR status. We retrospectively analyzed tumors of 450 HER2-positive breast cancer patients treated with chemotherapy and 1 year of trastuzumab. HR−/HER2+ tumors showed higher nuclear grade, less tubule formation, higher histologic grade, frequent apocrine features, diffuse and abundant lymphocytic infiltration, strong HER2 immunohistochemical staining (3+), higher average
HER2
copy number and
HER2
/
CEP17
ratio, the absence of
HER2
genetic heterogeneity, and greater p53 expression than HR+/HER2+ tumors. An inverse correlation was observed between estrogen receptor or progesterone receptor Allred score and average
HER2
copy number or
HER2
/
CEP17
ratio. The percentage of ductal carcinoma in situ (DCIS) within the tumor was negatively correlated with ER Allred score, but positively correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. Pathologic tumor size and DCIS percentage also showed a significant inverse correlation. Ratio of metastatic to total examined lymph node number was significantly correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. High pT stage (hazard ratio, 2.370;
p
= 0.027), the presence of lymphovascular invasion (hazard ratio, 2.806;
p
= 0.005), and HR negativity (hazard ratio, 2.202; 1.074–4.513;
p
= 0.031) were found to be independent prognostic indicators of poor disease-free survival. In conclusion, HR+/HER2+ and HR−/HER2+ breast cancer showed distinct histopathologic features that may be relevant to their distinct clinical behavior.</description><subject>Adult</subject><subject>Aged</subject><subject>Analysis</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Carcinoma, Intraductal, Noninfiltrating</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Disease-Free Survival</subject><subject>Epidermal growth factor</subject><subject>Female</subject><subject>Gene Amplification</subject><subject>Histopathology</subject><subject>Hormones</subject><subject>Hormones, Sex</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Neoplasm Grading</subject><subject>Oncology</subject><subject>Preclinical Study</subject><subject>Receptor, ErbB-2 - biosynthesis</subject><subject>Receptor, ErbB-2 - genetics</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Receptors, Progesterone - metabolism</subject><subject>Retrospective Studies</subject><subject>Trastuzumab</subject><subject>Tumor proteins</subject><subject>Tumor Suppressor Protein p53 - biosynthesis</subject><subject>Young Adult</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kttqFTEUhoModlt9AG9kQBBvpuYwOYx3pVQrFASp1yGTWbMnZSYZk4y2j-Bbm-2utvVALlbI-v6frORH6DnBRwRj-SYRzJu2xqSpaatYffUAbQiXrJaUyIdog4mQtVBYHKAnKV1ijFuJ28fogDaK4obQDfp-8S1Uo0s5LCaPYQpbZ800XVe9GwaI4HPZJTAJ0ttqDHEOHqoIFpYcYr2E5LL7CpXx_d9dD1vzs5vXOcRUOV-dnX6it6ouFuNcWeMtxKfo0WCmBM9u6iH6_O704uSsPv_4_sPJ8XltBRa57mzXCcuoZbxlvFFcsL4XpbKOC4E7RXsihTB4INwKA5w1DSUcM2GNUIqyQ_R677vE8GWFlPXskoVpMh7CmjThVDEmmhYX9OUf6GVYoy-321GSKt7K9pbamgm080PI0didqT5mqnyRaIko1NE_qLJ6mJ0t7za4cn5P8OqOYAQz5TGFac0u-HQfJHvQxpBShEEv0c0mXmuC9S4nep8TXXKidznRV0Xz4maytZuh_634FYwC0D2QSstvId4Z_b-uPwA_OMfd</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Lee, Hee Jin</creator><creator>Park, In Ah</creator><creator>Park, So Yeon</creator><creator>Seo, An Na</creator><creator>Lim, Bora</creator><creator>Chai, Yun</creator><creator>Song, In Hye</creator><creator>Kim, Na Eun</creator><creator>Kim, Joo Young</creator><creator>Yu, Jong Han</creator><creator>Ahn, Jin-Hee</creator><creator>Gong, Gyungyub</creator><general>Springer US</general><general>Springer</general><general>Springer Nature 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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20140601</creationdate><title>Two histopathologically different diseases: hormone receptor-positive and hormone receptor-negative tumors in HER2-positive breast cancer</title><author>Lee, Hee Jin ; Park, In Ah ; Park, So Yeon ; Seo, An Na ; Lim, Bora ; Chai, Yun ; Song, In Hye ; Kim, Na Eun ; Kim, Joo Young ; Yu, Jong Han ; Ahn, Jin-Hee ; Gong, Gyungyub</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c606t-bcbb6c32c3593548563dd64853b5660b82d1766a0f15c6ae5344215036ca68823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Analysis</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Carcinoma, Intraductal, Noninfiltrating</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Disease-Free Survival</topic><topic>Epidermal growth factor</topic><topic>Female</topic><topic>Gene Amplification</topic><topic>Histopathology</topic><topic>Hormones</topic><topic>Hormones, Sex</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Neoplasm Grading</topic><topic>Oncology</topic><topic>Preclinical Study</topic><topic>Receptor, ErbB-2 - biosynthesis</topic><topic>Receptor, ErbB-2 - genetics</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Receptors, Progesterone - metabolism</topic><topic>Retrospective Studies</topic><topic>Trastuzumab</topic><topic>Tumor proteins</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Hee Jin</creatorcontrib><creatorcontrib>Park, In Ah</creatorcontrib><creatorcontrib>Park, So Yeon</creatorcontrib><creatorcontrib>Seo, An Na</creatorcontrib><creatorcontrib>Lim, Bora</creatorcontrib><creatorcontrib>Chai, Yun</creatorcontrib><creatorcontrib>Song, In Hye</creatorcontrib><creatorcontrib>Kim, Na Eun</creatorcontrib><creatorcontrib>Kim, Joo Young</creatorcontrib><creatorcontrib>Yu, Jong Han</creatorcontrib><creatorcontrib>Ahn, Jin-Hee</creatorcontrib><creatorcontrib>Gong, Gyungyub</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Family Health Database (Proquest)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Hee Jin</au><au>Park, In Ah</au><au>Park, So Yeon</au><au>Seo, An Na</au><au>Lim, Bora</au><au>Chai, Yun</au><au>Song, In Hye</au><au>Kim, Na Eun</au><au>Kim, Joo Young</au><au>Yu, Jong Han</au><au>Ahn, Jin-Hee</au><au>Gong, Gyungyub</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two histopathologically different diseases: hormone receptor-positive and hormone receptor-negative tumors in HER2-positive breast cancer</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>145</volume><issue>3</issue><spage>615</spage><epage>623</epage><pages>615-623</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>The clinical behavior of human epidermal growth factor 2 (HER2)-positive breast cancer, including pathologic complete response rate and pattern of relapse and metastasis, differs substantially according to hormone receptor (HR) status. We investigated various histopathologic features of HER2-positive breast cancer and their correlation with HR status. We retrospectively analyzed tumors of 450 HER2-positive breast cancer patients treated with chemotherapy and 1 year of trastuzumab. HR−/HER2+ tumors showed higher nuclear grade, less tubule formation, higher histologic grade, frequent apocrine features, diffuse and abundant lymphocytic infiltration, strong HER2 immunohistochemical staining (3+), higher average
HER2
copy number and
HER2
/
CEP17
ratio, the absence of
HER2
genetic heterogeneity, and greater p53 expression than HR+/HER2+ tumors. An inverse correlation was observed between estrogen receptor or progesterone receptor Allred score and average
HER2
copy number or
HER2
/
CEP17
ratio. The percentage of ductal carcinoma in situ (DCIS) within the tumor was negatively correlated with ER Allred score, but positively correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. Pathologic tumor size and DCIS percentage also showed a significant inverse correlation. Ratio of metastatic to total examined lymph node number was significantly correlated with average
HER2
copy number and
HER2
/
CEP17
ratio. High pT stage (hazard ratio, 2.370;
p
= 0.027), the presence of lymphovascular invasion (hazard ratio, 2.806;
p
= 0.005), and HR negativity (hazard ratio, 2.202; 1.074–4.513;
p
= 0.031) were found to be independent prognostic indicators of poor disease-free survival. In conclusion, HR+/HER2+ and HR−/HER2+ breast cancer showed distinct histopathologic features that may be relevant to their distinct clinical behavior.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>24820412</pmid><doi>10.1007/s10549-014-2983-x</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Analysis Antibodies, Monoclonal, Humanized - therapeutic use Antineoplastic Agents - therapeutic use Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - pathology Cancer Cancer research Cancer therapies Carcinoma, Intraductal, Noninfiltrating Care and treatment Chemotherapy Disease-Free Survival Epidermal growth factor Female Gene Amplification Histopathology Hormones Hormones, Sex Humans Immunohistochemistry Medicine Medicine & Public Health Middle Aged Neoplasm Grading Oncology Preclinical Study Receptor, ErbB-2 - biosynthesis Receptor, ErbB-2 - genetics Receptors, Estrogen - metabolism Receptors, Progesterone - metabolism Retrospective Studies Trastuzumab Tumor proteins Tumor Suppressor Protein p53 - biosynthesis Young Adult |
title | Two histopathologically different diseases: hormone receptor-positive and hormone receptor-negative tumors in HER2-positive breast cancer |
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