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Cumulative risk of second primary contralateral breast cancer in BRCA1 / BRCA2 mutation carriers with a first breast cancer: A systematic review and meta-analysis
Abstract BRCA1/2 mutation carriers are at a higher risk of breast cancer and of subsequent contralateral breast cancer (CBC). This study aims to evaluate the evidence of the effect of the BRCA1/2 -carriership on CBC cumulative risk in female breast cancer patients. The literature was searched in Pub...
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Published in: | Breast (Edinburgh) 2014-12, Vol.23 (6), p.721-742 |
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container_title | Breast (Edinburgh) |
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creator | Molina-Montes, Esther Pérez-Nevot, Beatriz Pollán, Marina Sánchez-Cantalejo, Emilio Espín, Jaime Sánchez, María-José |
description | Abstract BRCA1/2 mutation carriers are at a higher risk of breast cancer and of subsequent contralateral breast cancer (CBC). This study aims to evaluate the evidence of the effect of the BRCA1/2 -carriership on CBC cumulative risk in female breast cancer patients. The literature was searched in Pubmed and Embase up to June 2013 for studies on CBC risk after a first primary invasive breast cancer in female BRCA 1/2 mutation carriers. A qualitative synthesis was carried out and the methodological quality of the studies evaluated. Cumulative risks of CBC after 5, 10 and 15 years since the first breast cancer diagnosis were pooled by BRCA1/2 mutation status. A total number of 20 articles, out of 1324 retrieved through the search, met the inclusion criteria: 18 retrospective and 2 prospective cohort studies. Cumulative risks of up to five studies were pooled. The cumulative 5-years risk of CBC for BRCA 1 and BRCA 2 mutation carriers was 15% (95% CI: 9.5%–20%) and 9% (95% CI: 5%–14%), respectively. This risk increases with time since diagnosis of the first breast cancer; the 10-years risk increased up to 27% and 19%, respectively. The 5-years cumulative risk was remarkably lower in non- BRCA carriers (3%; 95% CI: 2%–5%) and remained so over subsequent years (5%; 95% CI: 3%–7%). In conclusion, risk of CBC increases with length of time after the first breast cancer diagnosis in BRCA 1/2 mutation carriers. Studies addressing the impact of treatment-related factors and clinical characteristics of the first breast cancer on this risk are warranted. |
doi_str_mv | 10.1016/j.breast.2014.10.005 |
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This study aims to evaluate the evidence of the effect of the BRCA1/2 -carriership on CBC cumulative risk in female breast cancer patients. The literature was searched in Pubmed and Embase up to June 2013 for studies on CBC risk after a first primary invasive breast cancer in female BRCA 1/2 mutation carriers. A qualitative synthesis was carried out and the methodological quality of the studies evaluated. Cumulative risks of CBC after 5, 10 and 15 years since the first breast cancer diagnosis were pooled by BRCA1/2 mutation status. A total number of 20 articles, out of 1324 retrieved through the search, met the inclusion criteria: 18 retrospective and 2 prospective cohort studies. Cumulative risks of up to five studies were pooled. The cumulative 5-years risk of CBC for BRCA 1 and BRCA 2 mutation carriers was 15% (95% CI: 9.5%–20%) and 9% (95% CI: 5%–14%), respectively. This risk increases with time since diagnosis of the first breast cancer; the 10-years risk increased up to 27% and 19%, respectively. The 5-years cumulative risk was remarkably lower in non- BRCA carriers (3%; 95% CI: 2%–5%) and remained so over subsequent years (5%; 95% CI: 3%–7%). In conclusion, risk of CBC increases with length of time after the first breast cancer diagnosis in BRCA 1/2 mutation carriers. Studies addressing the impact of treatment-related factors and clinical characteristics of the first breast cancer on this risk are warranted.</description><identifier>ISSN: 0960-9776</identifier><identifier>EISSN: 1532-3080</identifier><identifier>DOI: 10.1016/j.breast.2014.10.005</identifier><identifier>PMID: 25467311</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Breast neoplasms ; Breast Neoplasms - genetics ; Contralateral ; Female ; Genes, BRCA1 ; Genes, BRCA2 ; Genetic Predisposition to Disease ; Hematology, Oncology and Palliative Medicine ; Heterozygote ; Humans ; Multiple primary ; Mutation ; Neoplasms, Second Primary - genetics ; Risk ; Systematic review</subject><ispartof>Breast (Edinburgh), 2014-12, Vol.23 (6), p.721-742</ispartof><rights>Elsevier Ltd</rights><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-d54ea5118f170f8024d641693772aa9b221cad617d905667202534175383433</citedby><cites>FETCH-LOGICAL-c487t-d54ea5118f170f8024d641693772aa9b221cad617d905667202534175383433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25467311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Molina-Montes, Esther</creatorcontrib><creatorcontrib>Pérez-Nevot, Beatriz</creatorcontrib><creatorcontrib>Pollán, Marina</creatorcontrib><creatorcontrib>Sánchez-Cantalejo, Emilio</creatorcontrib><creatorcontrib>Espín, Jaime</creatorcontrib><creatorcontrib>Sánchez, María-José</creatorcontrib><title>Cumulative risk of second primary contralateral breast cancer in BRCA1 / BRCA2 mutation carriers with a first breast cancer: A systematic review and meta-analysis</title><title>Breast (Edinburgh)</title><addtitle>Breast</addtitle><description>Abstract BRCA1/2 mutation carriers are at a higher risk of breast cancer and of subsequent contralateral breast cancer (CBC). This study aims to evaluate the evidence of the effect of the BRCA1/2 -carriership on CBC cumulative risk in female breast cancer patients. The literature was searched in Pubmed and Embase up to June 2013 for studies on CBC risk after a first primary invasive breast cancer in female BRCA 1/2 mutation carriers. A qualitative synthesis was carried out and the methodological quality of the studies evaluated. Cumulative risks of CBC after 5, 10 and 15 years since the first breast cancer diagnosis were pooled by BRCA1/2 mutation status. A total number of 20 articles, out of 1324 retrieved through the search, met the inclusion criteria: 18 retrospective and 2 prospective cohort studies. Cumulative risks of up to five studies were pooled. The cumulative 5-years risk of CBC for BRCA 1 and BRCA 2 mutation carriers was 15% (95% CI: 9.5%–20%) and 9% (95% CI: 5%–14%), respectively. This risk increases with time since diagnosis of the first breast cancer; the 10-years risk increased up to 27% and 19%, respectively. The 5-years cumulative risk was remarkably lower in non- BRCA carriers (3%; 95% CI: 2%–5%) and remained so over subsequent years (5%; 95% CI: 3%–7%). In conclusion, risk of CBC increases with length of time after the first breast cancer diagnosis in BRCA 1/2 mutation carriers. Studies addressing the impact of treatment-related factors and clinical characteristics of the first breast cancer on this risk are warranted.</description><subject>Breast neoplasms</subject><subject>Breast Neoplasms - genetics</subject><subject>Contralateral</subject><subject>Female</subject><subject>Genes, BRCA1</subject><subject>Genes, BRCA2</subject><subject>Genetic Predisposition to Disease</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Heterozygote</subject><subject>Humans</subject><subject>Multiple primary</subject><subject>Mutation</subject><subject>Neoplasms, Second Primary - genetics</subject><subject>Risk</subject><subject>Systematic review</subject><issn>0960-9776</issn><issn>1532-3080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFUstuFDEQtBCIbAJ_gJCPXGbTfs9wQNqsICBFQiLcLa-nR3gzj2B7Eu3v8KV42AUJLlzccquqS13VhLxisGbA9OV-vYvoUl5zYLK01gDqCVkxJXgloIanZAWNhqoxRp-R85T2ANAIXT8nZ1xJbQRjK_JjOw9z73J4QBpDuqNTRxP6aWzpfQyDiwdaPjm6gsHy0qMo9W70GGkY6dWX7YbRy1-V02HOZdg0FkCMAWOijyF_o452IRbaX-y3dEPTIWUcCsXTiA8BH6kr0gNmV7nR9YcU0gvyrHN9wpenekFuP7z_uv1Y3Xy-_rTd3FRe1iZXrZLoFGN1xwx0NXDZasl0I4zhzjU7zpl3rWambUBpbThwJSQzStRCCnFB3hyn3sfp-4wp2yEkj33vRpzmZJlW0oCopSpQeYT6OKUUsbMnqywDu2Rj9_a4qF2yWbolm0J7fVKYdwO2f0i_wyiAd0cAli2LF9EmH7A41YaIPtt2Cv9T-HeA78MYvOvv8IBpP82xeFp2sYlbsLfLfSznwSQAq5UUPwGA0rZ0</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>Molina-Montes, Esther</creator><creator>Pérez-Nevot, Beatriz</creator><creator>Pollán, Marina</creator><creator>Sánchez-Cantalejo, Emilio</creator><creator>Espín, Jaime</creator><creator>Sánchez, María-José</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20141201</creationdate><title>Cumulative risk of second primary contralateral breast cancer in BRCA1 / BRCA2 mutation carriers with a first breast cancer: A systematic review and meta-analysis</title><author>Molina-Montes, Esther ; Pérez-Nevot, Beatriz ; Pollán, Marina ; Sánchez-Cantalejo, Emilio ; Espín, Jaime ; Sánchez, María-José</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-d54ea5118f170f8024d641693772aa9b221cad617d905667202534175383433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Breast neoplasms</topic><topic>Breast Neoplasms - genetics</topic><topic>Contralateral</topic><topic>Female</topic><topic>Genes, BRCA1</topic><topic>Genes, BRCA2</topic><topic>Genetic Predisposition to Disease</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Heterozygote</topic><topic>Humans</topic><topic>Multiple primary</topic><topic>Mutation</topic><topic>Neoplasms, Second Primary - genetics</topic><topic>Risk</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Molina-Montes, Esther</creatorcontrib><creatorcontrib>Pérez-Nevot, Beatriz</creatorcontrib><creatorcontrib>Pollán, Marina</creatorcontrib><creatorcontrib>Sánchez-Cantalejo, Emilio</creatorcontrib><creatorcontrib>Espín, Jaime</creatorcontrib><creatorcontrib>Sánchez, María-José</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>Breast (Edinburgh)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Molina-Montes, Esther</au><au>Pérez-Nevot, Beatriz</au><au>Pollán, Marina</au><au>Sánchez-Cantalejo, Emilio</au><au>Espín, Jaime</au><au>Sánchez, María-José</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cumulative risk of second primary contralateral breast cancer in BRCA1 / BRCA2 mutation carriers with a first breast cancer: A systematic review and meta-analysis</atitle><jtitle>Breast (Edinburgh)</jtitle><addtitle>Breast</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>23</volume><issue>6</issue><spage>721</spage><epage>742</epage><pages>721-742</pages><issn>0960-9776</issn><eissn>1532-3080</eissn><abstract>Abstract BRCA1/2 mutation carriers are at a higher risk of breast cancer and of subsequent contralateral breast cancer (CBC). This study aims to evaluate the evidence of the effect of the BRCA1/2 -carriership on CBC cumulative risk in female breast cancer patients. The literature was searched in Pubmed and Embase up to June 2013 for studies on CBC risk after a first primary invasive breast cancer in female BRCA 1/2 mutation carriers. A qualitative synthesis was carried out and the methodological quality of the studies evaluated. Cumulative risks of CBC after 5, 10 and 15 years since the first breast cancer diagnosis were pooled by BRCA1/2 mutation status. A total number of 20 articles, out of 1324 retrieved through the search, met the inclusion criteria: 18 retrospective and 2 prospective cohort studies. Cumulative risks of up to five studies were pooled. The cumulative 5-years risk of CBC for BRCA 1 and BRCA 2 mutation carriers was 15% (95% CI: 9.5%–20%) and 9% (95% CI: 5%–14%), respectively. This risk increases with time since diagnosis of the first breast cancer; the 10-years risk increased up to 27% and 19%, respectively. The 5-years cumulative risk was remarkably lower in non- BRCA carriers (3%; 95% CI: 2%–5%) and remained so over subsequent years (5%; 95% CI: 3%–7%). In conclusion, risk of CBC increases with length of time after the first breast cancer diagnosis in BRCA 1/2 mutation carriers. Studies addressing the impact of treatment-related factors and clinical characteristics of the first breast cancer on this risk are warranted.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>25467311</pmid><doi>10.1016/j.breast.2014.10.005</doi><tpages>22</tpages></addata></record> |
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subjects | Breast neoplasms Breast Neoplasms - genetics Contralateral Female Genes, BRCA1 Genes, BRCA2 Genetic Predisposition to Disease Hematology, Oncology and Palliative Medicine Heterozygote Humans Multiple primary Mutation Neoplasms, Second Primary - genetics Risk Systematic review |
title | Cumulative risk of second primary contralateral breast cancer in BRCA1 / BRCA2 mutation carriers with a first breast cancer: A systematic review and meta-analysis |
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