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Impact of the 21-gene recurrence score on outcome in patients with invasive lobular carcinoma of the breast
Purpose Invasive lobular carcinoma (ILC) of the breast has unique clinicopathologic characteristics, compared to invasive ductal carcinoma. The role of the 21-gene Recurrence Score (RS) has not been clearly defined for ILC. We sought to determine the prognostic value of RS and the impact of adjuvant...
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Published in: | Breast cancer research and treatment 2017-10, Vol.165 (3), p.757-763 |
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description | Purpose
Invasive lobular carcinoma (ILC) of the breast has unique clinicopathologic characteristics, compared to invasive ductal carcinoma. The role of the 21-gene Recurrence Score (RS) has not been clearly defined for ILC. We sought to determine the prognostic value of RS and the impact of adjuvant chemotherapy on long-term survival in patients with ILC.
Methods
Utilizing the Surveillance, Epidemiology and End Results database from 2004 to 2013, we identified records of women aged 18–74 years, diagnosed with estrogen receptor (ER)-positive ILC (stage I to III) with RS available. We categorized patients into risk groups based on the traditional RS cutoffs and into those of the Trial Assigning Individualized Options for Treatment (TAILORx). Five-year breast cancer-specific survival (BCSS) was analyzed using the Kaplan–Meier method and Cox proportional hazards models.
Results
Of the 7316 women included, 21% were in the low-risk; 71%, intermediate-risk; and 8%, high-risk groups as per TAILORx RS cutoffs. The 5-year BCSS was 99% in the low-risk, 99% in the intermediate-risk, and 96% in the high-risk groups. A high-risk RS as per TAILORx cutoff was independently associated with increased mortality (hazard ratio [HR] of death 2.37, 95% confidence interval [CI] 1.14–4.95) when compared to a low-risk RS. In both the high-risk and intermediate-risk groups, adjuvant chemotherapy was not significantly associated with the HR of death (high-risk, HR 1.14, 95% CI 0.55–2.38; intermediate-risk, HR 1.08, 95% CI 0.62–1.87).
Conclusion
For patients with ER-positive ILC, 8% were in the high-risk and 72% were in the intermediate-risk groups as per the TAILORx RS cutoffs. In the high-risk group, the RS predicted a lower 5-year BCSS. Adjuvant chemotherapy did not seem to confer a survival benefit for either the intermediate- or the high-risk cohorts. |
doi_str_mv | 10.1007/s10549-017-4355-9 |
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Invasive lobular carcinoma (ILC) of the breast has unique clinicopathologic characteristics, compared to invasive ductal carcinoma. The role of the 21-gene Recurrence Score (RS) has not been clearly defined for ILC. We sought to determine the prognostic value of RS and the impact of adjuvant chemotherapy on long-term survival in patients with ILC.
Methods
Utilizing the Surveillance, Epidemiology and End Results database from 2004 to 2013, we identified records of women aged 18–74 years, diagnosed with estrogen receptor (ER)-positive ILC (stage I to III) with RS available. We categorized patients into risk groups based on the traditional RS cutoffs and into those of the Trial Assigning Individualized Options for Treatment (TAILORx). Five-year breast cancer-specific survival (BCSS) was analyzed using the Kaplan–Meier method and Cox proportional hazards models.
Results
Of the 7316 women included, 21% were in the low-risk; 71%, intermediate-risk; and 8%, high-risk groups as per TAILORx RS cutoffs. The 5-year BCSS was 99% in the low-risk, 99% in the intermediate-risk, and 96% in the high-risk groups. A high-risk RS as per TAILORx cutoff was independently associated with increased mortality (hazard ratio [HR] of death 2.37, 95% confidence interval [CI] 1.14–4.95) when compared to a low-risk RS. In both the high-risk and intermediate-risk groups, adjuvant chemotherapy was not significantly associated with the HR of death (high-risk, HR 1.14, 95% CI 0.55–2.38; intermediate-risk, HR 1.08, 95% CI 0.62–1.87).
Conclusion
For patients with ER-positive ILC, 8% were in the high-risk and 72% were in the intermediate-risk groups as per the TAILORx RS cutoffs. In the high-risk group, the RS predicted a lower 5-year BCSS. Adjuvant chemotherapy did not seem to confer a survival benefit for either the intermediate- or the high-risk cohorts.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-017-4355-9</identifier><identifier>PMID: 28647915</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adjuvant treatment ; Analysis ; Breast cancer ; Brief Report ; Cancer ; Cancer research ; Chemotherapy ; Diseases ; Epidemiology ; Estrogen ; Estrogen receptors ; Genes ; Genetic aspects ; Health risk assessment ; Invasiveness ; Medicine ; Medicine & Public Health ; Mortality ; Oncology ; Relapse ; Risk groups ; Survival</subject><ispartof>Breast cancer research and treatment, 2017-10, Vol.165 (3), p.757-763</ispartof><rights>Springer Science+Business Media, LLC 2017</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Breast Cancer Research and Treatment is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-1ecc4fff94b168103933b2ccfb37d1a67011d978101b28980c0c4dba0d58bf023</citedby><cites>FETCH-LOGICAL-c470t-1ecc4fff94b168103933b2ccfb37d1a67011d978101b28980c0c4dba0d58bf023</cites><orcidid>0000-0002-2628-0720</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28647915$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kizy, Scott</creatorcontrib><creatorcontrib>Huang, Jing Li</creatorcontrib><creatorcontrib>Marmor, Schelomo</creatorcontrib><creatorcontrib>Tuttle, Todd M.</creatorcontrib><creatorcontrib>Hui, Jane Yuet Ching</creatorcontrib><title>Impact of the 21-gene recurrence score on outcome in patients with invasive lobular carcinoma of the breast</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose
Invasive lobular carcinoma (ILC) of the breast has unique clinicopathologic characteristics, compared to invasive ductal carcinoma. The role of the 21-gene Recurrence Score (RS) has not been clearly defined for ILC. We sought to determine the prognostic value of RS and the impact of adjuvant chemotherapy on long-term survival in patients with ILC.
Methods
Utilizing the Surveillance, Epidemiology and End Results database from 2004 to 2013, we identified records of women aged 18–74 years, diagnosed with estrogen receptor (ER)-positive ILC (stage I to III) with RS available. We categorized patients into risk groups based on the traditional RS cutoffs and into those of the Trial Assigning Individualized Options for Treatment (TAILORx). Five-year breast cancer-specific survival (BCSS) was analyzed using the Kaplan–Meier method and Cox proportional hazards models.
Results
Of the 7316 women included, 21% were in the low-risk; 71%, intermediate-risk; and 8%, high-risk groups as per TAILORx RS cutoffs. The 5-year BCSS was 99% in the low-risk, 99% in the intermediate-risk, and 96% in the high-risk groups. A high-risk RS as per TAILORx cutoff was independently associated with increased mortality (hazard ratio [HR] of death 2.37, 95% confidence interval [CI] 1.14–4.95) when compared to a low-risk RS. In both the high-risk and intermediate-risk groups, adjuvant chemotherapy was not significantly associated with the HR of death (high-risk, HR 1.14, 95% CI 0.55–2.38; intermediate-risk, HR 1.08, 95% CI 0.62–1.87).
Conclusion
For patients with ER-positive ILC, 8% were in the high-risk and 72% were in the intermediate-risk groups as per the TAILORx RS cutoffs. In the high-risk group, the RS predicted a lower 5-year BCSS. Adjuvant chemotherapy did not seem to confer a survival benefit for either the intermediate- or the high-risk cohorts.</description><subject>Adjuvant treatment</subject><subject>Analysis</subject><subject>Breast cancer</subject><subject>Brief Report</subject><subject>Cancer</subject><subject>Cancer research</subject><subject>Chemotherapy</subject><subject>Diseases</subject><subject>Epidemiology</subject><subject>Estrogen</subject><subject>Estrogen receptors</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Health risk assessment</subject><subject>Invasiveness</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mortality</subject><subject>Oncology</subject><subject>Relapse</subject><subject>Risk groups</subject><subject>Survival</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kl1rFTEQhoMo9lj9Ad5IQBBvts7sVzaXpfhRKHij1yGbnZyTupsck2zFf28Op9VWlFwEZp73nQx5GXuJcIYA4l1C6FpZAYqqbbquko_YBjvRVKJG8ZhtAHtR9QP0J-xZStcAIAXIp-ykHvpWSOw27Nvlstcm82B53hGvsdqSJx7JrDGSN8STCZF48Dys2YSFuPN8r7MjnxP_4fKuFG50cjfE5zCus47c6GicD4u-sx0j6ZSfsydWz4le3N6n7OuH918uPlVXnz9eXpxfVaYVkCskY1prrWxH7AeERjbNWBtjx0ZMqHsBiJMUpYNjPcgBDJh2GjVM3TBaqJtT9vbou4_h-0opq8UlQ_OsPYU1KZTYDA1IEAV9_Rd6Hdboy-sK1UiUQwv4h9rqmZTzNuSozcFUnXfQDnUH9WHs2T-ociZanAmerCv1B4I39wQ70nPepTCv2QWfHoJ4BE0MKUWyah_douNPhaAOSVDHJKiSBHVIgpJF8-p2s3VcaPqtuPv6AtRHIJWW31K8t_p_XX8BSRa7FA</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Kizy, Scott</creator><creator>Huang, Jing Li</creator><creator>Marmor, Schelomo</creator><creator>Tuttle, Todd M.</creator><creator>Hui, Jane Yuet Ching</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><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>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2628-0720</orcidid></search><sort><creationdate>20171001</creationdate><title>Impact of the 21-gene recurrence score on outcome in patients with invasive lobular carcinoma of the breast</title><author>Kizy, Scott ; Huang, Jing Li ; Marmor, Schelomo ; Tuttle, Todd M. ; Hui, Jane Yuet Ching</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-1ecc4fff94b168103933b2ccfb37d1a67011d978101b28980c0c4dba0d58bf023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adjuvant treatment</topic><topic>Analysis</topic><topic>Breast cancer</topic><topic>Brief Report</topic><topic>Cancer</topic><topic>Cancer research</topic><topic>Chemotherapy</topic><topic>Diseases</topic><topic>Epidemiology</topic><topic>Estrogen</topic><topic>Estrogen receptors</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Health risk assessment</topic><topic>Invasiveness</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mortality</topic><topic>Oncology</topic><topic>Relapse</topic><topic>Risk groups</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kizy, Scott</creatorcontrib><creatorcontrib>Huang, Jing Li</creatorcontrib><creatorcontrib>Marmor, Schelomo</creatorcontrib><creatorcontrib>Tuttle, Todd M.</creatorcontrib><creatorcontrib>Hui, Jane Yuet Ching</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>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</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>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 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>Kizy, Scott</au><au>Huang, Jing Li</au><au>Marmor, Schelomo</au><au>Tuttle, Todd M.</au><au>Hui, Jane Yuet Ching</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of the 21-gene recurrence score on outcome in patients with invasive lobular carcinoma of the breast</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>165</volume><issue>3</issue><spage>757</spage><epage>763</epage><pages>757-763</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><abstract>Purpose
Invasive lobular carcinoma (ILC) of the breast has unique clinicopathologic characteristics, compared to invasive ductal carcinoma. The role of the 21-gene Recurrence Score (RS) has not been clearly defined for ILC. We sought to determine the prognostic value of RS and the impact of adjuvant chemotherapy on long-term survival in patients with ILC.
Methods
Utilizing the Surveillance, Epidemiology and End Results database from 2004 to 2013, we identified records of women aged 18–74 years, diagnosed with estrogen receptor (ER)-positive ILC (stage I to III) with RS available. We categorized patients into risk groups based on the traditional RS cutoffs and into those of the Trial Assigning Individualized Options for Treatment (TAILORx). Five-year breast cancer-specific survival (BCSS) was analyzed using the Kaplan–Meier method and Cox proportional hazards models.
Results
Of the 7316 women included, 21% were in the low-risk; 71%, intermediate-risk; and 8%, high-risk groups as per TAILORx RS cutoffs. The 5-year BCSS was 99% in the low-risk, 99% in the intermediate-risk, and 96% in the high-risk groups. A high-risk RS as per TAILORx cutoff was independently associated with increased mortality (hazard ratio [HR] of death 2.37, 95% confidence interval [CI] 1.14–4.95) when compared to a low-risk RS. In both the high-risk and intermediate-risk groups, adjuvant chemotherapy was not significantly associated with the HR of death (high-risk, HR 1.14, 95% CI 0.55–2.38; intermediate-risk, HR 1.08, 95% CI 0.62–1.87).
Conclusion
For patients with ER-positive ILC, 8% were in the high-risk and 72% were in the intermediate-risk groups as per the TAILORx RS cutoffs. In the high-risk group, the RS predicted a lower 5-year BCSS. Adjuvant chemotherapy did not seem to confer a survival benefit for either the intermediate- or the high-risk cohorts.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>28647915</pmid><doi>10.1007/s10549-017-4355-9</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-2628-0720</orcidid></addata></record> |
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subjects | Adjuvant treatment Analysis Breast cancer Brief Report Cancer Cancer research Chemotherapy Diseases Epidemiology Estrogen Estrogen receptors Genes Genetic aspects Health risk assessment Invasiveness Medicine Medicine & Public Health Mortality Oncology Relapse Risk groups Survival |
title | Impact of the 21-gene recurrence score on outcome in patients with invasive lobular carcinoma of the breast |
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