Pregnancy-associated breast cancer: the influence of gestational age
Whether pregnancy-associated breast cancer (PABC) arise before or during pregnancy and whether this histopathology is affected by gestational age are currently unclear. The present study assesses the influence of gestational age and lactation on the histopathologic profile of PABC. We identified 744...
Gespeichert in:
Veröffentlicht in: | Endocrine-related cancer 2022-03, Vol.29 (3), p.129-138 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 138 |
---|---|
container_issue | 3 |
container_start_page | 129 |
container_title | Endocrine-related cancer |
container_volume | 29 |
creator | Suelmann, Britt B M van Dooijeweert, Carmen Bakhuis, Carsten F J Linn, Sabine van der Wall, Elsken van Diest, Paul J |
description | Whether pregnancy-associated breast cancer (PABC) arise before or during pregnancy and whether this histopathology is affected by gestational age are currently unclear. The present study assesses the influence of gestational age and lactation on the histopathologic profile of PABC. We identified 744 patients with PABC (defined as breast cancer during pregnancy or 6 months following delivery). Histopathologic features were compared between pregnant and postpartum patients. We found that age at diagnosis was 34.2 years, and a majority of cancers were diagnosed during pregnancy (71.3%). Within pregnant patients, tumors were significantly more often estrogen receptor (ER)-negative in second and third trimesters (57.4%), as compared to first trimesters (41.9%) (P = 0.036). Similarly, a progesterone receptor (PR)-negative status was reported significantly less often within first trimesters (38.0%) compared to second and third trimesters (57.1%) (P = 0.032). For human EGF receptor 2 status, no significant differences were observed between gestational trimesters or lactating vs non-lactating patients. In postpartum patients, grade III tumors were found in over 80%, with high percentages of ER-negative tumors reaching 63% in those lactating vs 49% in non-lactating patients. This study demonstrates the varying histopathologic profile of PABC by gestational age and lactation status. Second- and third-trimester cancers display most typically the common ER/PR-negative phenotype, which is commonly reported in the literature. The increased ER-negative status and percentage grade III tumors in lactating vs non-lactating patients also suggest the presence of additional factors further diversifying histology. This indicates the need for clear definitions of PABC and the role of potential subgroups, which may provide a stepping stone for further in-depth research into PABC-carcinogenesis. |
doi_str_mv | 10.1530/ERC-21-0206 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2612737953</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2612737953</sourcerecordid><originalsourceid>FETCH-LOGICAL-b359t-30103c25a127270b6f3abc1de83c0cedbe637cc419b40ac66d38ec35c4cbeaa43</originalsourceid><addsrcrecordid>eNp90E1LxDAQBuAgiqurJ-9S8CJINck0aetN1k9YUETPJZlO1yzdVpP24L83y6oHD54yGR5ehpexI8HPhQJ-cfM8S6VIueR6i-2JLC9TXUixHWdQcc-LYsL2Q1hyznWh1C6bQFaC0iD32PWTp0VnOvxMTQg9OjNQnVhPJgwJxj35y2R4o8R1TTtS_Cd9kywoDGZwfWfaxCzogO00pg10-P1O2evtzcvsPp0_3j3MruapBVUOKXDBAaUyQuYy51Y3YCyKmgpAjlRb0pAjZqK0GTeodQ0FISjM0JIxGUzZ6Sb33fcfY7yhWrmA1Lamo34MldQxGfJSQaQnf-iyH328d61ASZ3roozqbKPQ9yF4aqp371bGf1aCV-tyq1huJUW1Ljfq4-_M0a6o_rU_bUYgNsC6PqCjbnCNQ_Nv6BcZtIPR</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2635267689</pqid></control><display><type>article</type><title>Pregnancy-associated breast cancer: the influence of gestational age</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><source>Society for Endocrinology Journals</source><creator>Suelmann, Britt B M ; van Dooijeweert, Carmen ; Bakhuis, Carsten F J ; Linn, Sabine ; van der Wall, Elsken ; van Diest, Paul J</creator><creatorcontrib>Suelmann, Britt B M ; van Dooijeweert, Carmen ; Bakhuis, Carsten F J ; Linn, Sabine ; van der Wall, Elsken ; van Diest, Paul J</creatorcontrib><description>Whether pregnancy-associated breast cancer (PABC) arise before or during pregnancy and whether this histopathology is affected by gestational age are currently unclear. The present study assesses the influence of gestational age and lactation on the histopathologic profile of PABC. We identified 744 patients with PABC (defined as breast cancer during pregnancy or 6 months following delivery). Histopathologic features were compared between pregnant and postpartum patients. We found that age at diagnosis was 34.2 years, and a majority of cancers were diagnosed during pregnancy (71.3%). Within pregnant patients, tumors were significantly more often estrogen receptor (ER)-negative in second and third trimesters (57.4%), as compared to first trimesters (41.9%) (P = 0.036). Similarly, a progesterone receptor (PR)-negative status was reported significantly less often within first trimesters (38.0%) compared to second and third trimesters (57.1%) (P = 0.032). For human EGF receptor 2 status, no significant differences were observed between gestational trimesters or lactating vs non-lactating patients. In postpartum patients, grade III tumors were found in over 80%, with high percentages of ER-negative tumors reaching 63% in those lactating vs 49% in non-lactating patients. This study demonstrates the varying histopathologic profile of PABC by gestational age and lactation status. Second- and third-trimester cancers display most typically the common ER/PR-negative phenotype, which is commonly reported in the literature. The increased ER-negative status and percentage grade III tumors in lactating vs non-lactating patients also suggest the presence of additional factors further diversifying histology. This indicates the need for clear definitions of PABC and the role of potential subgroups, which may provide a stepping stone for further in-depth research into PABC-carcinogenesis.</description><identifier>ISSN: 1351-0088</identifier><identifier>EISSN: 1479-6821</identifier><identifier>DOI: 10.1530/ERC-21-0206</identifier><identifier>PMID: 34935632</identifier><language>eng</language><publisher>England: Bioscientifica Ltd</publisher><subject>Age ; Breast cancer ; Breast Neoplasms - pathology ; Breastfeeding & lactation ; Carcinogenesis ; Estrogen receptors ; Female ; Gestational Age ; Humans ; Lactation ; Phenotypes ; Postpartum ; Pregnancy ; Pregnancy Complications, Neoplastic - diagnosis ; Pregnancy Complications, Neoplastic - pathology ; Progesterone ; Prognosis ; Tumors</subject><ispartof>Endocrine-related cancer, 2022-03, Vol.29 (3), p.129-138</ispartof><rights>Society for Endocrinology</rights><rights>Copyright Society for Endocrinology & BioScientifica Ltd. Mar 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b359t-30103c25a127270b6f3abc1de83c0cedbe637cc419b40ac66d38ec35c4cbeaa43</citedby><orcidid>0000-0001-8030-4335 ; 0000-0002-7155-3337 ; 0000-0002-2344-9252</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3936,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34935632$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suelmann, Britt B M</creatorcontrib><creatorcontrib>van Dooijeweert, Carmen</creatorcontrib><creatorcontrib>Bakhuis, Carsten F J</creatorcontrib><creatorcontrib>Linn, Sabine</creatorcontrib><creatorcontrib>van der Wall, Elsken</creatorcontrib><creatorcontrib>van Diest, Paul J</creatorcontrib><title>Pregnancy-associated breast cancer: the influence of gestational age</title><title>Endocrine-related cancer</title><addtitle>Endocr Relat Cancer</addtitle><description>Whether pregnancy-associated breast cancer (PABC) arise before or during pregnancy and whether this histopathology is affected by gestational age are currently unclear. The present study assesses the influence of gestational age and lactation on the histopathologic profile of PABC. We identified 744 patients with PABC (defined as breast cancer during pregnancy or 6 months following delivery). Histopathologic features were compared between pregnant and postpartum patients. We found that age at diagnosis was 34.2 years, and a majority of cancers were diagnosed during pregnancy (71.3%). Within pregnant patients, tumors were significantly more often estrogen receptor (ER)-negative in second and third trimesters (57.4%), as compared to first trimesters (41.9%) (P = 0.036). Similarly, a progesterone receptor (PR)-negative status was reported significantly less often within first trimesters (38.0%) compared to second and third trimesters (57.1%) (P = 0.032). For human EGF receptor 2 status, no significant differences were observed between gestational trimesters or lactating vs non-lactating patients. In postpartum patients, grade III tumors were found in over 80%, with high percentages of ER-negative tumors reaching 63% in those lactating vs 49% in non-lactating patients. This study demonstrates the varying histopathologic profile of PABC by gestational age and lactation status. Second- and third-trimester cancers display most typically the common ER/PR-negative phenotype, which is commonly reported in the literature. The increased ER-negative status and percentage grade III tumors in lactating vs non-lactating patients also suggest the presence of additional factors further diversifying histology. This indicates the need for clear definitions of PABC and the role of potential subgroups, which may provide a stepping stone for further in-depth research into PABC-carcinogenesis.</description><subject>Age</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - pathology</subject><subject>Breastfeeding & lactation</subject><subject>Carcinogenesis</subject><subject>Estrogen receptors</subject><subject>Female</subject><subject>Gestational Age</subject><subject>Humans</subject><subject>Lactation</subject><subject>Phenotypes</subject><subject>Postpartum</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Neoplastic - diagnosis</subject><subject>Pregnancy Complications, Neoplastic - pathology</subject><subject>Progesterone</subject><subject>Prognosis</subject><subject>Tumors</subject><issn>1351-0088</issn><issn>1479-6821</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90E1LxDAQBuAgiqurJ-9S8CJINck0aetN1k9YUETPJZlO1yzdVpP24L83y6oHD54yGR5ehpexI8HPhQJ-cfM8S6VIueR6i-2JLC9TXUixHWdQcc-LYsL2Q1hyznWh1C6bQFaC0iD32PWTp0VnOvxMTQg9OjNQnVhPJgwJxj35y2R4o8R1TTtS_Cd9kywoDGZwfWfaxCzogO00pg10-P1O2evtzcvsPp0_3j3MruapBVUOKXDBAaUyQuYy51Y3YCyKmgpAjlRb0pAjZqK0GTeodQ0FISjM0JIxGUzZ6Sb33fcfY7yhWrmA1Lamo34MldQxGfJSQaQnf-iyH328d61ASZ3roozqbKPQ9yF4aqp371bGf1aCV-tyq1huJUW1Ljfq4-_M0a6o_rU_bUYgNsC6PqCjbnCNQ_Nv6BcZtIPR</recordid><startdate>20220301</startdate><enddate>20220301</enddate><creator>Suelmann, Britt B M</creator><creator>van Dooijeweert, Carmen</creator><creator>Bakhuis, Carsten F J</creator><creator>Linn, Sabine</creator><creator>van der Wall, Elsken</creator><creator>van Diest, Paul J</creator><general>Bioscientifica Ltd</general><general>Society for Endocrinology & BioScientifica Ltd</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><orcidid>https://orcid.org/0000-0001-8030-4335</orcidid><orcidid>https://orcid.org/0000-0002-7155-3337</orcidid><orcidid>https://orcid.org/0000-0002-2344-9252</orcidid></search><sort><creationdate>20220301</creationdate><title>Pregnancy-associated breast cancer: the influence of gestational age</title><author>Suelmann, Britt B M ; van Dooijeweert, Carmen ; Bakhuis, Carsten F J ; Linn, Sabine ; van der Wall, Elsken ; van Diest, Paul J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b359t-30103c25a127270b6f3abc1de83c0cedbe637cc419b40ac66d38ec35c4cbeaa43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Age</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - pathology</topic><topic>Breastfeeding & lactation</topic><topic>Carcinogenesis</topic><topic>Estrogen receptors</topic><topic>Female</topic><topic>Gestational Age</topic><topic>Humans</topic><topic>Lactation</topic><topic>Phenotypes</topic><topic>Postpartum</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Neoplastic - diagnosis</topic><topic>Pregnancy Complications, Neoplastic - pathology</topic><topic>Progesterone</topic><topic>Prognosis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suelmann, Britt B M</creatorcontrib><creatorcontrib>van Dooijeweert, Carmen</creatorcontrib><creatorcontrib>Bakhuis, Carsten F J</creatorcontrib><creatorcontrib>Linn, Sabine</creatorcontrib><creatorcontrib>van der Wall, Elsken</creatorcontrib><creatorcontrib>van Diest, Paul J</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>Endocrine-related cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suelmann, Britt B M</au><au>van Dooijeweert, Carmen</au><au>Bakhuis, Carsten F J</au><au>Linn, Sabine</au><au>van der Wall, Elsken</au><au>van Diest, Paul J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pregnancy-associated breast cancer: the influence of gestational age</atitle><jtitle>Endocrine-related cancer</jtitle><addtitle>Endocr Relat Cancer</addtitle><date>2022-03-01</date><risdate>2022</risdate><volume>29</volume><issue>3</issue><spage>129</spage><epage>138</epage><pages>129-138</pages><issn>1351-0088</issn><eissn>1479-6821</eissn><abstract>Whether pregnancy-associated breast cancer (PABC) arise before or during pregnancy and whether this histopathology is affected by gestational age are currently unclear. The present study assesses the influence of gestational age and lactation on the histopathologic profile of PABC. We identified 744 patients with PABC (defined as breast cancer during pregnancy or 6 months following delivery). Histopathologic features were compared between pregnant and postpartum patients. We found that age at diagnosis was 34.2 years, and a majority of cancers were diagnosed during pregnancy (71.3%). Within pregnant patients, tumors were significantly more often estrogen receptor (ER)-negative in second and third trimesters (57.4%), as compared to first trimesters (41.9%) (P = 0.036). Similarly, a progesterone receptor (PR)-negative status was reported significantly less often within first trimesters (38.0%) compared to second and third trimesters (57.1%) (P = 0.032). For human EGF receptor 2 status, no significant differences were observed between gestational trimesters or lactating vs non-lactating patients. In postpartum patients, grade III tumors were found in over 80%, with high percentages of ER-negative tumors reaching 63% in those lactating vs 49% in non-lactating patients. This study demonstrates the varying histopathologic profile of PABC by gestational age and lactation status. Second- and third-trimester cancers display most typically the common ER/PR-negative phenotype, which is commonly reported in the literature. The increased ER-negative status and percentage grade III tumors in lactating vs non-lactating patients also suggest the presence of additional factors further diversifying histology. This indicates the need for clear definitions of PABC and the role of potential subgroups, which may provide a stepping stone for further in-depth research into PABC-carcinogenesis.</abstract><cop>England</cop><pub>Bioscientifica Ltd</pub><pmid>34935632</pmid><doi>10.1530/ERC-21-0206</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8030-4335</orcidid><orcidid>https://orcid.org/0000-0002-7155-3337</orcidid><orcidid>https://orcid.org/0000-0002-2344-9252</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1351-0088 |
ispartof | Endocrine-related cancer, 2022-03, Vol.29 (3), p.129-138 |
issn | 1351-0088 1479-6821 |
language | eng |
recordid | cdi_proquest_miscellaneous_2612737953 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection; Society for Endocrinology Journals |
subjects | Age Breast cancer Breast Neoplasms - pathology Breastfeeding & lactation Carcinogenesis Estrogen receptors Female Gestational Age Humans Lactation Phenotypes Postpartum Pregnancy Pregnancy Complications, Neoplastic - diagnosis Pregnancy Complications, Neoplastic - pathology Progesterone Prognosis Tumors |
title | Pregnancy-associated breast cancer: the influence of gestational age |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T15%3A39%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pregnancy-associated%20breast%20cancer:%20the%20influence%20of%20gestational%20age&rft.jtitle=Endocrine-related%20cancer&rft.au=Suelmann,%20Britt%20B%20M&rft.date=2022-03-01&rft.volume=29&rft.issue=3&rft.spage=129&rft.epage=138&rft.pages=129-138&rft.issn=1351-0088&rft.eissn=1479-6821&rft_id=info:doi/10.1530/ERC-21-0206&rft_dat=%3Cproquest_cross%3E2612737953%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2635267689&rft_id=info:pmid/34935632&rfr_iscdi=true |