76-gene signature defines high-risk patients that benefit from adjuvant tamoxifen therapy

Purpose To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups identified by the previously established prognostic 76-gene signature. Methods In 300 lymph node-negative (LNN), estrogen receptor-positive (ER+) breast cancer patients (136 treated with adjuvant tamo...

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Veröffentlicht in:Breast cancer research and treatment 2009-07, Vol.116 (2), p.303-309
Hauptverfasser: Zhang, Yi, Sieuwerts, Anieta M, McGreevy, Michelle, Casey, Graham, Cufer, Tanja, Paradiso, Angelo, Harbeck, Nadia, Span, Paul N, Hicks, David G, Crowe, Joseph, Tubbs, Raymond R, Budd, G. Thomas, Lyons, Joanne, Sweep, Fred C. G. J, Schmitt, Manfred, Schittulli, Francesco, Golouh, Rastko, Talantov, Dmitri, Wang, Yixin, Foekens, John A
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container_end_page 309
container_issue 2
container_start_page 303
container_title Breast cancer research and treatment
container_volume 116
creator Zhang, Yi
Sieuwerts, Anieta M
McGreevy, Michelle
Casey, Graham
Cufer, Tanja
Paradiso, Angelo
Harbeck, Nadia
Span, Paul N
Hicks, David G
Crowe, Joseph
Tubbs, Raymond R
Budd, G. Thomas
Lyons, Joanne
Sweep, Fred C. G. J
Schmitt, Manfred
Schittulli, Francesco
Golouh, Rastko
Talantov, Dmitri
Wang, Yixin
Foekens, John A
description Purpose To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups identified by the previously established prognostic 76-gene signature. Methods In 300 lymph node-negative (LNN), estrogen receptor-positive (ER+) breast cancer patients (136 treated with adjuvant tamoxifen, 164 having received no systemic adjuvant therapy), distant metastasis-free survival (DMFS) as a function of the 76-gene signature was determined in a multicenter fashion. Results In 136 tamoxifen-treated patients, the 76-gene signature identified a group of patients with a poor prognosis [hazard ratio (HR), 4.62; P = 0.0248]. These patients showed a 12.3% absolute benefit of tamoxifen in 10-year DMFS (HR, 0.52; P = 0.0318) compared with untreated high-risk patients. This represented a 71% increase in relative benefit compared with the 7.2% absolute benefit observed for all 300 patients without using the gene signature. In the low-risk group there was no significant 10-year DMFS benefit of tamoxifen. Conclusions The 76-gene signature defines high-risk patients who benefit from adjuvant tamoxifen therapy. Although we did not study the value of chemotherapy in this study, low-risk patients identified by the 76-gene signature have a prognosis good enough that chemotherapy would be difficult to justify. The prognosis of these patients is sufficiently good, in fact, that a disease-free benefit for tamoxifen therapy is difficult to prove, though benefits in terms of loco-regional relapse and a reduction in risk for contralateral breast cancer might justify hormonal therapy in these patients.
doi_str_mv 10.1007/s10549-008-0183-2
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Thomas ; Lyons, Joanne ; Sweep, Fred C. G. J ; Schmitt, Manfred ; Schittulli, Francesco ; Golouh, Rastko ; Talantov, Dmitri ; Wang, Yixin ; Foekens, John A</creator><creatorcontrib>Zhang, Yi ; Sieuwerts, Anieta M ; McGreevy, Michelle ; Casey, Graham ; Cufer, Tanja ; Paradiso, Angelo ; Harbeck, Nadia ; Span, Paul N ; Hicks, David G ; Crowe, Joseph ; Tubbs, Raymond R ; Budd, G. Thomas ; Lyons, Joanne ; Sweep, Fred C. G. J ; Schmitt, Manfred ; Schittulli, Francesco ; Golouh, Rastko ; Talantov, Dmitri ; Wang, Yixin ; Foekens, John A</creatorcontrib><description>Purpose To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups identified by the previously established prognostic 76-gene signature. Methods In 300 lymph node-negative (LNN), estrogen receptor-positive (ER+) breast cancer patients (136 treated with adjuvant tamoxifen, 164 having received no systemic adjuvant therapy), distant metastasis-free survival (DMFS) as a function of the 76-gene signature was determined in a multicenter fashion. Results In 136 tamoxifen-treated patients, the 76-gene signature identified a group of patients with a poor prognosis [hazard ratio (HR), 4.62; P = 0.0248]. These patients showed a 12.3% absolute benefit of tamoxifen in 10-year DMFS (HR, 0.52; P = 0.0318) compared with untreated high-risk patients. This represented a 71% increase in relative benefit compared with the 7.2% absolute benefit observed for all 300 patients without using the gene signature. In the low-risk group there was no significant 10-year DMFS benefit of tamoxifen. Conclusions The 76-gene signature defines high-risk patients who benefit from adjuvant tamoxifen therapy. Although we did not study the value of chemotherapy in this study, low-risk patients identified by the 76-gene signature have a prognosis good enough that chemotherapy would be difficult to justify. The prognosis of these patients is sufficiently good, in fact, that a disease-free benefit for tamoxifen therapy is difficult to prove, though benefits in terms of loco-regional relapse and a reduction in risk for contralateral breast cancer might justify hormonal therapy in these patients.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-008-0183-2</identifier><identifier>PMID: 18821012</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Adult ; Aged ; Antineoplastic Agents, Hormonal - therapeutic use ; Biological and medical sciences ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Cancer research ; Cancer therapies ; Chemotherapy, Adjuvant ; Clinical Trial ; Clinical trials ; Drug therapy ; Female ; Gene Expression ; Genetics ; Gynecology. Andrology. Obstetrics ; Humans ; Kaplan-Meier Estimate ; Mammary gland diseases ; Medical prognosis ; Medical sciences ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Neoplasm Staging ; Oncology ; Prognosis ; Risk Factors ; Selective Estrogen Receptor Modulators - therapeutic use ; Tamoxifen - therapeutic use ; Tumors</subject><ispartof>Breast cancer research and treatment, 2009-07, Vol.116 (2), p.303-309</ispartof><rights>Springer Science+Business Media, LLC. 2008</rights><rights>2009 INIST-CNRS</rights><rights>Springer Science+Business Media, LLC. 2009</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-715d784d8b08d0c18a8b5c9d8432a3748e2c7d74838856d060ccb7ab079596f93</citedby><cites>FETCH-LOGICAL-c531t-715d784d8b08d0c18a8b5c9d8432a3748e2c7d74838856d060ccb7ab079596f93</cites><orcidid>0000-0002-9744-7372</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10549-008-0183-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10549-008-0183-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21781779$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18821012$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00478265$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Yi</creatorcontrib><creatorcontrib>Sieuwerts, Anieta M</creatorcontrib><creatorcontrib>McGreevy, Michelle</creatorcontrib><creatorcontrib>Casey, Graham</creatorcontrib><creatorcontrib>Cufer, Tanja</creatorcontrib><creatorcontrib>Paradiso, Angelo</creatorcontrib><creatorcontrib>Harbeck, Nadia</creatorcontrib><creatorcontrib>Span, Paul N</creatorcontrib><creatorcontrib>Hicks, David G</creatorcontrib><creatorcontrib>Crowe, Joseph</creatorcontrib><creatorcontrib>Tubbs, Raymond R</creatorcontrib><creatorcontrib>Budd, G. Thomas</creatorcontrib><creatorcontrib>Lyons, Joanne</creatorcontrib><creatorcontrib>Sweep, Fred C. G. J</creatorcontrib><creatorcontrib>Schmitt, Manfred</creatorcontrib><creatorcontrib>Schittulli, Francesco</creatorcontrib><creatorcontrib>Golouh, Rastko</creatorcontrib><creatorcontrib>Talantov, Dmitri</creatorcontrib><creatorcontrib>Wang, Yixin</creatorcontrib><creatorcontrib>Foekens, John A</creatorcontrib><title>76-gene signature defines high-risk patients that benefit from adjuvant tamoxifen therapy</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups identified by the previously established prognostic 76-gene signature. Methods In 300 lymph node-negative (LNN), estrogen receptor-positive (ER+) breast cancer patients (136 treated with adjuvant tamoxifen, 164 having received no systemic adjuvant therapy), distant metastasis-free survival (DMFS) as a function of the 76-gene signature was determined in a multicenter fashion. Results In 136 tamoxifen-treated patients, the 76-gene signature identified a group of patients with a poor prognosis [hazard ratio (HR), 4.62; P = 0.0248]. These patients showed a 12.3% absolute benefit of tamoxifen in 10-year DMFS (HR, 0.52; P = 0.0318) compared with untreated high-risk patients. This represented a 71% increase in relative benefit compared with the 7.2% absolute benefit observed for all 300 patients without using the gene signature. In the low-risk group there was no significant 10-year DMFS benefit of tamoxifen. Conclusions The 76-gene signature defines high-risk patients who benefit from adjuvant tamoxifen therapy. Although we did not study the value of chemotherapy in this study, low-risk patients identified by the 76-gene signature have a prognosis good enough that chemotherapy would be difficult to justify. The prognosis of these patients is sufficiently good, in fact, that a disease-free benefit for tamoxifen therapy is difficult to prove, though benefits in terms of loco-regional relapse and a reduction in risk for contralateral breast cancer might justify hormonal therapy in these patients.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Chemotherapy, Adjuvant</subject><subject>Clinical Trial</subject><subject>Clinical trials</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Genetics</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Mammary gland diseases</subject><subject>Medical prognosis</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>Risk Factors</subject><subject>Selective Estrogen Receptor Modulators - therapeutic use</subject><subject>Tamoxifen - therapeutic use</subject><subject>Tumors</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFksFu1DAQhi0EokvhAbhAhAQSB8PYjmPnWFVAkVbiAD1wsiaOk_WSTRbbqejb45BVK3GA00jjb8b_zD-EPGfwjgGo95GBLGsKoCkwLSh_QDZMKkEVZ-oh2QCrFK00VGfkSYx7AKgV1I_JGdOaM2B8Q76rivZudEX0_YhpDq5oXedHF4ud73c0-PijOGLybkyxSDtMRZPxzqeiC9OhwHY_3-CYioSH6Zfv3JghF_B4-5Q86nCI7tkpnpPrjx--XV7R7ZdPny8vttRKwRJVTLZKl61uQLdgmUbdSFu3uhQchSq141a1OQqtZdVCBdY2ChtQtayrrhbn5O3ad4eDOQZ_wHBrJvTm6mJrlhxAqTSv5A3L7JuVPYbp5-xiMgcfrRsGHN00R1MpoVhe3n9BDkxIrcoMvvoL3E9zGPPAhjNeZsl_ILZCNkwxBtfd6WRgFifN6mSWqs3ipOG55sWp8dwcXHtfcbIuA69PAEaLQxdwtD7ecfkCNFNq2Q9fuZifxt6Fe4X_-v3lWtThZLDPV2Cuvy5D55MqZdYgfgMDn7yD</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Zhang, Yi</creator><creator>Sieuwerts, Anieta M</creator><creator>McGreevy, Michelle</creator><creator>Casey, Graham</creator><creator>Cufer, Tanja</creator><creator>Paradiso, Angelo</creator><creator>Harbeck, Nadia</creator><creator>Span, Paul N</creator><creator>Hicks, David G</creator><creator>Crowe, Joseph</creator><creator>Tubbs, Raymond R</creator><creator>Budd, G. 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Thomas ; Lyons, Joanne ; Sweep, Fred C. G. J ; Schmitt, Manfred ; Schittulli, Francesco ; Golouh, Rastko ; Talantov, Dmitri ; Wang, Yixin ; Foekens, John A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-715d784d8b08d0c18a8b5c9d8432a3748e2c7d74838856d060ccb7ab079596f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents, Hormonal - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Chemotherapy, Adjuvant</topic><topic>Clinical Trial</topic><topic>Clinical trials</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Genetics</topic><topic>Gynecology. Andrology. 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Thomas</au><au>Lyons, Joanne</au><au>Sweep, Fred C. G. J</au><au>Schmitt, Manfred</au><au>Schittulli, Francesco</au><au>Golouh, Rastko</au><au>Talantov, Dmitri</au><au>Wang, Yixin</au><au>Foekens, John A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>76-gene signature defines high-risk patients that benefit from adjuvant tamoxifen therapy</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2009-07-01</date><risdate>2009</risdate><volume>116</volume><issue>2</issue><spage>303</spage><epage>309</epage><pages>303-309</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>Purpose To assess the benefit from adjuvant systemic tamoxifen therapy in breast cancer risk groups identified by the previously established prognostic 76-gene signature. Methods In 300 lymph node-negative (LNN), estrogen receptor-positive (ER+) breast cancer patients (136 treated with adjuvant tamoxifen, 164 having received no systemic adjuvant therapy), distant metastasis-free survival (DMFS) as a function of the 76-gene signature was determined in a multicenter fashion. Results In 136 tamoxifen-treated patients, the 76-gene signature identified a group of patients with a poor prognosis [hazard ratio (HR), 4.62; P = 0.0248]. These patients showed a 12.3% absolute benefit of tamoxifen in 10-year DMFS (HR, 0.52; P = 0.0318) compared with untreated high-risk patients. This represented a 71% increase in relative benefit compared with the 7.2% absolute benefit observed for all 300 patients without using the gene signature. In the low-risk group there was no significant 10-year DMFS benefit of tamoxifen. Conclusions The 76-gene signature defines high-risk patients who benefit from adjuvant tamoxifen therapy. Although we did not study the value of chemotherapy in this study, low-risk patients identified by the 76-gene signature have a prognosis good enough that chemotherapy would be difficult to justify. The prognosis of these patients is sufficiently good, in fact, that a disease-free benefit for tamoxifen therapy is difficult to prove, though benefits in terms of loco-regional relapse and a reduction in risk for contralateral breast cancer might justify hormonal therapy in these patients.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>18821012</pmid><doi>10.1007/s10549-008-0183-2</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-9744-7372</orcidid><oa>free_for_read</oa></addata></record>
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1573-7217
language eng
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source MEDLINE; SpringerLink Journals (MCLS)
subjects Adult
Aged
Antineoplastic Agents, Hormonal - therapeutic use
Biological and medical sciences
Breast cancer
Breast Neoplasms - drug therapy
Breast Neoplasms - genetics
Breast Neoplasms - pathology
Cancer research
Cancer therapies
Chemotherapy, Adjuvant
Clinical Trial
Clinical trials
Drug therapy
Female
Gene Expression
Genetics
Gynecology. Andrology. Obstetrics
Humans
Kaplan-Meier Estimate
Mammary gland diseases
Medical prognosis
Medical sciences
Medicine
Medicine & Public Health
Middle Aged
Neoplasm Staging
Oncology
Prognosis
Risk Factors
Selective Estrogen Receptor Modulators - therapeutic use
Tamoxifen - therapeutic use
Tumors
title 76-gene signature defines high-risk patients that benefit from adjuvant tamoxifen therapy
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