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FEC versus sequential docetaxel followed by epirubicin/cyclophosphamide as adjuvant chemotherapy in women with axillary node-positive early breast cancer: a randomized study of the Hellenic Oncology Research Group (HORG)
A randomized multicenter phase III study was conducted to compare the sequential docetaxel followed by epirubicin/cyclophosphamide combination with that of FEC regimen as adjuvant chemotherapy in women with axillary node-positive early breast cancer. Seven hundred and fifty-six women with axillary l...
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Published in: | Breast cancer research and treatment 2010-01, Vol.119 (1), p.95-104 |
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creator | Polyzos, Aristides Malamos, Nikolaos Boukovinas, Ioannis Adamou, Adamos Ziras, Nikolaos Kalbakis, Kostas Kakolyris, Stylianos Syrigos, Kostas Papakotoulas, Pavlos Kouroussis, Charalambos Karvounis, Nikolaos Vamvakas, Lambros Christophyllakis, Charalambos Athanasiadis, Athanasios Varthalitis, Ioannis Georgoulias, Vassilis Mavroudis, Dimitris |
description | A randomized multicenter phase III study was conducted to compare the sequential docetaxel followed by epirubicin/cyclophosphamide combination with that of FEC regimen as adjuvant chemotherapy in women with axillary node-positive early breast cancer. Seven hundred and fifty-six women with axillary lymph node-positive breast cancer were randomized to receive either 4 cycles of docetaxel (100 mg/m²) followed by 4 cycles of epirubicin (75 mg/m²) plus cyclophosphamide (700 mg/m²) (experimental arm) or 6 cycles of FEC (epirubicin 75 mg/m², cyclophosphamide 700 mg/m², and 5-fluorouracil 700 mg/m²; control arm). All regimes were administered every 3 weeks. The primary end point was five-year disease-free survival (DFS). After a median follow-up period of 5 years, 233 (30.8%) relapses had occurred (108 and 125 in the experimental and control arms, respectively; P = 0.181). The five-year DFS was 72.6% (95% CI 63.8-81.3%) and 67.2% (95% CI 58.0-76.4%) for women randomized in the experimental and control arms, respectively (P = 0.041; log rank test). There was no difference in the overall survival between the two arms (83.8 and 81.4% in the experimental and control arms, respectively; P = 0.533). The experimental arm was associated with increased neutropenia requiring administration of granulocyte colony-stimulating factor in 90.5% of the patients as compared with 74.1% in the control arm (P = 0.0001). The sequential docetaxel followed by epirubicin/cyclophosphamide adjuvant chemotherapy regimen resulted in improved five-year DFS in women with axillary node-positive early breast cancer at the expense of increased but manageable myelotoxicity. |
doi_str_mv | 10.1007/s10549-009-0468-0 |
format | article |
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Seven hundred and fifty-six women with axillary lymph node-positive breast cancer were randomized to receive either 4 cycles of docetaxel (100 mg/m²) followed by 4 cycles of epirubicin (75 mg/m²) plus cyclophosphamide (700 mg/m²) (experimental arm) or 6 cycles of FEC (epirubicin 75 mg/m², cyclophosphamide 700 mg/m², and 5-fluorouracil 700 mg/m²; control arm). All regimes were administered every 3 weeks. The primary end point was five-year disease-free survival (DFS). After a median follow-up period of 5 years, 233 (30.8%) relapses had occurred (108 and 125 in the experimental and control arms, respectively; P = 0.181). The five-year DFS was 72.6% (95% CI 63.8-81.3%) and 67.2% (95% CI 58.0-76.4%) for women randomized in the experimental and control arms, respectively (P = 0.041; log rank test). There was no difference in the overall survival between the two arms (83.8 and 81.4% in the experimental and control arms, respectively; P = 0.533). The experimental arm was associated with increased neutropenia requiring administration of granulocyte colony-stimulating factor in 90.5% of the patients as compared with 74.1% in the control arm (P = 0.0001). The sequential docetaxel followed by epirubicin/cyclophosphamide adjuvant chemotherapy regimen resulted in improved five-year DFS in women with axillary node-positive early breast cancer at the expense of increased but manageable myelotoxicity.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-009-0468-0</identifier><identifier>PMID: 19636702</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Adenocarcinoma - drug therapy ; Adjuvant treatment ; Adult ; Aged ; Anthracyclines ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Cancer ; Cancer research ; Cancer therapies ; Chemotherapy ; Chemotherapy, Adjuvant - methods ; Clinical Trial ; Clinical trials ; Cyclophosphamide ; Cyclophosphamide - administration & dosage ; Cyclophosphamide - therapeutic use ; Disease-Free Survival ; Epirubicin - administration & dosage ; Epirubicin - therapeutic use ; Female ; Fluorouracil ; Fluorouracil - therapeutic use ; Gynecology. Andrology. Obstetrics ; Humans ; Lymphatic Metastasis ; Lymphatic system ; Mammary gland diseases ; Medical sciences ; Medicine ; Medicine & Public Health ; Middle Aged ; Oncology ; Oncology, Experimental ; Time Factors ; Treatment Outcome ; Tumors ; Women</subject><ispartof>Breast cancer research and treatment, 2010-01, Vol.119 (1), p.95-104</ispartof><rights>Springer Science+Business Media, LLC. 2009</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 Springer</rights><rights>Springer Science+Business Media, LLC. 2010</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-c599t-5aa69ff9d5fa9e5cf9ca0ecc44d6eb667aaf9909f2946c5c40d2113f8d39d48c3</citedby><cites>FETCH-LOGICAL-c599t-5aa69ff9d5fa9e5cf9ca0ecc44d6eb667aaf9909f2946c5c40d2113f8d39d48c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22347012$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19636702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00535384$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Polyzos, Aristides</creatorcontrib><creatorcontrib>Malamos, Nikolaos</creatorcontrib><creatorcontrib>Boukovinas, Ioannis</creatorcontrib><creatorcontrib>Adamou, Adamos</creatorcontrib><creatorcontrib>Ziras, Nikolaos</creatorcontrib><creatorcontrib>Kalbakis, Kostas</creatorcontrib><creatorcontrib>Kakolyris, Stylianos</creatorcontrib><creatorcontrib>Syrigos, Kostas</creatorcontrib><creatorcontrib>Papakotoulas, Pavlos</creatorcontrib><creatorcontrib>Kouroussis, Charalambos</creatorcontrib><creatorcontrib>Karvounis, Nikolaos</creatorcontrib><creatorcontrib>Vamvakas, Lambros</creatorcontrib><creatorcontrib>Christophyllakis, Charalambos</creatorcontrib><creatorcontrib>Athanasiadis, Athanasios</creatorcontrib><creatorcontrib>Varthalitis, Ioannis</creatorcontrib><creatorcontrib>Georgoulias, Vassilis</creatorcontrib><creatorcontrib>Mavroudis, Dimitris</creatorcontrib><title>FEC versus sequential docetaxel followed by epirubicin/cyclophosphamide as adjuvant chemotherapy in women with axillary node-positive early breast cancer: a randomized study of the Hellenic Oncology Research Group (HORG)</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>A randomized multicenter phase III study was conducted to compare the sequential docetaxel followed by epirubicin/cyclophosphamide combination with that of FEC regimen as adjuvant chemotherapy in women with axillary node-positive early breast cancer. Seven hundred and fifty-six women with axillary lymph node-positive breast cancer were randomized to receive either 4 cycles of docetaxel (100 mg/m²) followed by 4 cycles of epirubicin (75 mg/m²) plus cyclophosphamide (700 mg/m²) (experimental arm) or 6 cycles of FEC (epirubicin 75 mg/m², cyclophosphamide 700 mg/m², and 5-fluorouracil 700 mg/m²; control arm). All regimes were administered every 3 weeks. The primary end point was five-year disease-free survival (DFS). After a median follow-up period of 5 years, 233 (30.8%) relapses had occurred (108 and 125 in the experimental and control arms, respectively; P = 0.181). The five-year DFS was 72.6% (95% CI 63.8-81.3%) and 67.2% (95% CI 58.0-76.4%) for women randomized in the experimental and control arms, respectively (P = 0.041; log rank test). There was no difference in the overall survival between the two arms (83.8 and 81.4% in the experimental and control arms, respectively; P = 0.533). The experimental arm was associated with increased neutropenia requiring administration of granulocyte colony-stimulating factor in 90.5% of the patients as compared with 74.1% in the control arm (P = 0.0001). The sequential docetaxel followed by epirubicin/cyclophosphamide adjuvant chemotherapy regimen resulted in improved five-year DFS in women with axillary node-positive early breast cancer at the expense of increased but manageable myelotoxicity.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adjuvant treatment</subject><subject>Adult</subject><subject>Aged</subject><subject>Anthracyclines</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Cancer</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant - methods</subject><subject>Clinical Trial</subject><subject>Clinical trials</subject><subject>Cyclophosphamide</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Disease-Free Survival</subject><subject>Epirubicin - administration & dosage</subject><subject>Epirubicin - therapeutic use</subject><subject>Female</subject><subject>Fluorouracil</subject><subject>Fluorouracil - therapeutic use</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Lymphatic Metastasis</subject><subject>Lymphatic system</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Oncology, Experimental</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Women</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kt1u1DAQhSMEomXhAbgBC8RPL9La-XHW3FVV20WqVKnQ62jWGW9cOXawk22XZ-Vh8CqrliKEIseS_Z0zPqNJkteMHjJKq6PAaFmIlNK4Cj5P6ZNkn5VVnlYZq54m-5TxKuVzyveSFyHc0AhWVDxP9pjgOa9otp_8Ojs9IWv0YQwk4I8R7aDBkMZJHOAODVHOGHeLDVluCPbaj0sttT2SG2lc37rQt9DpBgkEAs3NuAY7ENli54YWPfQboi25dR3Gvx5aAnfaGPAbYl2Dae-CHvQaCYI3G7L0CCHKwUr0XwgQD7Zxnf4Zy4dhbDbEKRJ9yQKNQaslubTSGbfakCsM0UO25Ny7sSefF5dX5wcvk2cKTMBXu32WXJ-dfj9ZpBeX519Pji9SWQoxpCUAF0qJplQgsJRKSKAoZVE0HJecVwBKCCpUJgouS1nQJmMsV_MmF00xl_ksOZh8WzB173UXA9YOdL04vqi3Z5SWeZnPizWL7KeJ7b2L7Q5D3ekgYx6w6MZQV3nBKs6YiOS7v8gbN3obg9QZywqezcXW7v0ErcBgra1ygwe5tayP85JnnG8rz5LDf1Dxa7DT0llUOp4_Enz8Q9AimKENzoyDdjY8BtkESu9C8Kju8zNab4e0noY0tiCuOKQ1jZo3u2DjssPmQbGbygh82AEQJBgVx0DqcM9lWV5UlG25bOJCvLIr9A8d-l_1t5NIgath5aPx9beMspyyiuXxCflv2FAKPg</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Polyzos, Aristides</creator><creator>Malamos, Nikolaos</creator><creator>Boukovinas, Ioannis</creator><creator>Adamou, Adamos</creator><creator>Ziras, Nikolaos</creator><creator>Kalbakis, Kostas</creator><creator>Kakolyris, Stylianos</creator><creator>Syrigos, Kostas</creator><creator>Papakotoulas, Pavlos</creator><creator>Kouroussis, Charalambos</creator><creator>Karvounis, Nikolaos</creator><creator>Vamvakas, Lambros</creator><creator>Christophyllakis, Charalambos</creator><creator>Athanasiadis, Athanasios</creator><creator>Varthalitis, Ioannis</creator><creator>Georgoulias, Vassilis</creator><creator>Mavroudis, Dimitris</creator><general>Boston : Springer US</general><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><general>Springer Verlag</general><scope>FBQ</scope><scope>IQODW</scope><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><scope>1XC</scope><scope>VOOES</scope></search><sort><creationdate>20100101</creationdate><title>FEC versus sequential docetaxel followed by epirubicin/cyclophosphamide as adjuvant chemotherapy in women with axillary node-positive early breast cancer: a randomized study of the Hellenic Oncology Research Group (HORG)</title><author>Polyzos, Aristides ; Malamos, Nikolaos ; Boukovinas, Ioannis ; Adamou, Adamos ; Ziras, Nikolaos ; Kalbakis, Kostas ; Kakolyris, Stylianos ; Syrigos, Kostas ; Papakotoulas, Pavlos ; Kouroussis, Charalambos ; Karvounis, Nikolaos ; Vamvakas, Lambros ; Christophyllakis, Charalambos ; Athanasiadis, Athanasios ; Varthalitis, Ioannis ; Georgoulias, Vassilis ; Mavroudis, Dimitris</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c599t-5aa69ff9d5fa9e5cf9ca0ecc44d6eb667aaf9909f2946c5c40d2113f8d39d48c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adenocarcinoma - drug therapy</topic><topic>Adjuvant treatment</topic><topic>Adult</topic><topic>Aged</topic><topic>Anthracyclines</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Cancer</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Chemotherapy, Adjuvant - methods</topic><topic>Clinical Trial</topic><topic>Clinical trials</topic><topic>Cyclophosphamide</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>Disease-Free Survival</topic><topic>Epirubicin - administration & dosage</topic><topic>Epirubicin - therapeutic use</topic><topic>Female</topic><topic>Fluorouracil</topic><topic>Fluorouracil - therapeutic use</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Lymphatic Metastasis</topic><topic>Lymphatic system</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Oncology, Experimental</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Polyzos, Aristides</creatorcontrib><creatorcontrib>Malamos, Nikolaos</creatorcontrib><creatorcontrib>Boukovinas, Ioannis</creatorcontrib><creatorcontrib>Adamou, Adamos</creatorcontrib><creatorcontrib>Ziras, Nikolaos</creatorcontrib><creatorcontrib>Kalbakis, Kostas</creatorcontrib><creatorcontrib>Kakolyris, Stylianos</creatorcontrib><creatorcontrib>Syrigos, Kostas</creatorcontrib><creatorcontrib>Papakotoulas, Pavlos</creatorcontrib><creatorcontrib>Kouroussis, Charalambos</creatorcontrib><creatorcontrib>Karvounis, Nikolaos</creatorcontrib><creatorcontrib>Vamvakas, Lambros</creatorcontrib><creatorcontrib>Christophyllakis, Charalambos</creatorcontrib><creatorcontrib>Athanasiadis, Athanasios</creatorcontrib><creatorcontrib>Varthalitis, Ioannis</creatorcontrib><creatorcontrib>Georgoulias, Vassilis</creatorcontrib><creatorcontrib>Mavroudis, Dimitris</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: 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>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><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Polyzos, Aristides</au><au>Malamos, Nikolaos</au><au>Boukovinas, Ioannis</au><au>Adamou, Adamos</au><au>Ziras, Nikolaos</au><au>Kalbakis, Kostas</au><au>Kakolyris, Stylianos</au><au>Syrigos, Kostas</au><au>Papakotoulas, Pavlos</au><au>Kouroussis, Charalambos</au><au>Karvounis, Nikolaos</au><au>Vamvakas, Lambros</au><au>Christophyllakis, Charalambos</au><au>Athanasiadis, Athanasios</au><au>Varthalitis, Ioannis</au><au>Georgoulias, Vassilis</au><au>Mavroudis, Dimitris</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FEC versus sequential docetaxel followed by epirubicin/cyclophosphamide as adjuvant chemotherapy in women with axillary node-positive early breast cancer: a randomized study of the Hellenic Oncology Research Group (HORG)</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>119</volume><issue>1</issue><spage>95</spage><epage>104</epage><pages>95-104</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>A randomized multicenter phase III study was conducted to compare the sequential docetaxel followed by epirubicin/cyclophosphamide combination with that of FEC regimen as adjuvant chemotherapy in women with axillary node-positive early breast cancer. Seven hundred and fifty-six women with axillary lymph node-positive breast cancer were randomized to receive either 4 cycles of docetaxel (100 mg/m²) followed by 4 cycles of epirubicin (75 mg/m²) plus cyclophosphamide (700 mg/m²) (experimental arm) or 6 cycles of FEC (epirubicin 75 mg/m², cyclophosphamide 700 mg/m², and 5-fluorouracil 700 mg/m²; control arm). All regimes were administered every 3 weeks. The primary end point was five-year disease-free survival (DFS). After a median follow-up period of 5 years, 233 (30.8%) relapses had occurred (108 and 125 in the experimental and control arms, respectively; P = 0.181). The five-year DFS was 72.6% (95% CI 63.8-81.3%) and 67.2% (95% CI 58.0-76.4%) for women randomized in the experimental and control arms, respectively (P = 0.041; log rank test). There was no difference in the overall survival between the two arms (83.8 and 81.4% in the experimental and control arms, respectively; P = 0.533). The experimental arm was associated with increased neutropenia requiring administration of granulocyte colony-stimulating factor in 90.5% of the patients as compared with 74.1% in the control arm (P = 0.0001). The sequential docetaxel followed by epirubicin/cyclophosphamide adjuvant chemotherapy regimen resulted in improved five-year DFS in women with axillary node-positive early breast cancer at the expense of increased but manageable myelotoxicity.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>19636702</pmid><doi>10.1007/s10549-009-0468-0</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0167-6806 |
ispartof | Breast cancer research and treatment, 2010-01, Vol.119 (1), p.95-104 |
issn | 0167-6806 1573-7217 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_00535384v1 |
source | Springer Nature |
subjects | Adenocarcinoma - drug therapy Adjuvant treatment Adult Aged Anthracyclines Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Cancer Cancer research Cancer therapies Chemotherapy Chemotherapy, Adjuvant - methods Clinical Trial Clinical trials Cyclophosphamide Cyclophosphamide - administration & dosage Cyclophosphamide - therapeutic use Disease-Free Survival Epirubicin - administration & dosage Epirubicin - therapeutic use Female Fluorouracil Fluorouracil - therapeutic use Gynecology. Andrology. Obstetrics Humans Lymphatic Metastasis Lymphatic system Mammary gland diseases Medical sciences Medicine Medicine & Public Health Middle Aged Oncology Oncology, Experimental Time Factors Treatment Outcome Tumors Women |
title | FEC versus sequential docetaxel followed by epirubicin/cyclophosphamide as adjuvant chemotherapy in women with axillary node-positive early breast cancer: a randomized study of the Hellenic Oncology Research Group (HORG) |
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