A randomized study comparing docetaxel/cyclophosphamide (TC), 5-fluorouracil/epirubicin/cyclophosphamide (FEC) followed by TC, and TC followed by FEC for patients with hormone receptor-positive HER2-negative primary breast cancer

Purpose Our primary objective was to determine the benefit/risk of anthracycline-free regimens by comparing docetaxel + cyclophosphamide (TC) alone, fluorouracil + epirubicin + cyclophosphamide (FEC) followed by TC, or TC followed by FEC as a primary treatment for patients with HR-positive, HER2-neg...

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Veröffentlicht in:Breast cancer research and treatment 2020-04, Vol.180 (3), p.715-724
Hauptverfasser: Ishiguro, Hiroshi, Masuda, Norikazu, Sato, Nobuaki, Higaki, Kenji, Morimoto, Takashi, Yanagita, Yasuhiro, Mizutani, Makiko, Ohtani, Shoichiro, Kaneko, Koji, Fujisawa, Tomomi, Takahashi, Masato, Kadoya, Takayuki, Matsunami, Nobuki, Yamamoto, Yutaka, Ohno, Shinji, Takano, Toshimi, Morita, Satoshi, Tanaka-Mizuno, Sachiko, Toi, Masakazu
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container_issue 3
container_start_page 715
container_title Breast cancer research and treatment
container_volume 180
creator Ishiguro, Hiroshi
Masuda, Norikazu
Sato, Nobuaki
Higaki, Kenji
Morimoto, Takashi
Yanagita, Yasuhiro
Mizutani, Makiko
Ohtani, Shoichiro
Kaneko, Koji
Fujisawa, Tomomi
Takahashi, Masato
Kadoya, Takayuki
Matsunami, Nobuki
Yamamoto, Yutaka
Ohno, Shinji
Takano, Toshimi
Morita, Satoshi
Tanaka-Mizuno, Sachiko
Toi, Masakazu
description Purpose Our primary objective was to determine the benefit/risk of anthracycline-free regimens by comparing docetaxel + cyclophosphamide (TC) alone, fluorouracil + epirubicin + cyclophosphamide (FEC) followed by TC, or TC followed by FEC as a primary treatment for patients with HR-positive, HER2-negative BC. Methods We randomized patients with stage I–III HR-positive HER2-negative, operable BC to receive either six cycles of TC (TC6), three cycles of FEC followed by three cycles of TC (FEC-TC), or three cycles of TC followed by three cycles of FEC (TC-FEC). The primary endpoint was the pathological response. Secondary endpoints included clinical response, type of surgical procedure, recurrence, death, and adverse events (by NCI-Common Terminology Criteria for Adverse Events v.3.0). We conducted all statistical analyses using SAS Version 9.2. Results We enrolled 195 patients and analyzed data from 193 as the intention-to-treat population. Pathological complete response rates were numerically higher in the TC6 group than in the other groups ( p  = 0.321). The breast conservation rate was significantly higher in the TC6 group (73%) than in the other groups (FEC-TC 51%, TC-FEC 45%, p  = 0.007). Adverse events with grade > 3 were not common in the treatment groups ( p  = 0.569). The overall and distant disease-free survivals were similar among the groups with median follow-up of 5.80 years. Conclusions Despite similar long-term efficacy and safety profile, the higher breast conservation rate in the TC6 group suggests that preoperative chemotherapy without an anthracycline may benefit patients with HR-positive HER2-negative BC. Trial registration UMIN000003283 https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003873 .
doi_str_mv 10.1007/s10549-020-05590-w
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Methods We randomized patients with stage I–III HR-positive HER2-negative, operable BC to receive either six cycles of TC (TC6), three cycles of FEC followed by three cycles of TC (FEC-TC), or three cycles of TC followed by three cycles of FEC (TC-FEC). The primary endpoint was the pathological response. Secondary endpoints included clinical response, type of surgical procedure, recurrence, death, and adverse events (by NCI-Common Terminology Criteria for Adverse Events v.3.0). We conducted all statistical analyses using SAS Version 9.2. Results We enrolled 195 patients and analyzed data from 193 as the intention-to-treat population. Pathological complete response rates were numerically higher in the TC6 group than in the other groups ( p  = 0.321). The breast conservation rate was significantly higher in the TC6 group (73%) than in the other groups (FEC-TC 51%, TC-FEC 45%, p  = 0.007). Adverse events with grade &gt; 3 were not common in the treatment groups ( p  = 0.569). The overall and distant disease-free survivals were similar among the groups with median follow-up of 5.80 years. Conclusions Despite similar long-term efficacy and safety profile, the higher breast conservation rate in the TC6 group suggests that preoperative chemotherapy without an anthracycline may benefit patients with HR-positive HER2-negative BC. Trial registration UMIN000003283 https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003873 .</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-020-05590-w</identifier><identifier>PMID: 32170634</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>5-Fluorouracil ; Adult ; Aged ; Anthracycline ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; Cancer therapies ; Carcinoma, Ductal, Breast - drug therapy ; Carcinoma, Ductal, Breast - pathology ; Carcinoma, Lobular - drug therapy ; Carcinoma, Lobular - pathology ; Chemotherapy ; Clinical Trial ; Clinical trials ; Creatinine ; Cyclophosphamide ; Cyclophosphamide - administration &amp; dosage ; Docetaxel - administration &amp; dosage ; Drug dosages ; Edema ; Epirubicin ; Epirubicin - administration &amp; dosage ; ErbB-2 protein ; Estrogens ; Female ; Fluorouracil - administration &amp; dosage ; Follow-Up Studies ; Granulocytes ; Hemoglobin ; Humans ; Medical research ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Neutropenia ; Oncology ; Patients ; Peripheral neuropathy ; Prognosis ; Receptor, ErbB-2 - metabolism ; Receptors, Estrogen - metabolism ; Receptors, Progesterone - metabolism ; Registration ; Statistical analysis ; Survival Rate ; Terminology ; UMIN ; UMIN000003283 ; Young Adult</subject><ispartof>Breast cancer research and treatment, 2020-04, Vol.180 (3), p.715-724</ispartof><rights>The Author(s) 2020</rights><rights>Breast Cancer Research and Treatment is a copyright of Springer, (2020). All Rights Reserved. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-e9f61d02bf5f8dfb804465c0fec8de3e4e3ecfa9f049d1502029a231dcd0d9e13</citedby><cites>FETCH-LOGICAL-c474t-e9f61d02bf5f8dfb804465c0fec8de3e4e3ecfa9f049d1502029a231dcd0d9e13</cites><orcidid>0000-0002-9859-5932</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/s10549-020-05590-w$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10549-020-05590-w$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,778,782,883,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32170634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishiguro, Hiroshi</creatorcontrib><creatorcontrib>Masuda, Norikazu</creatorcontrib><creatorcontrib>Sato, Nobuaki</creatorcontrib><creatorcontrib>Higaki, Kenji</creatorcontrib><creatorcontrib>Morimoto, Takashi</creatorcontrib><creatorcontrib>Yanagita, Yasuhiro</creatorcontrib><creatorcontrib>Mizutani, Makiko</creatorcontrib><creatorcontrib>Ohtani, Shoichiro</creatorcontrib><creatorcontrib>Kaneko, Koji</creatorcontrib><creatorcontrib>Fujisawa, Tomomi</creatorcontrib><creatorcontrib>Takahashi, Masato</creatorcontrib><creatorcontrib>Kadoya, Takayuki</creatorcontrib><creatorcontrib>Matsunami, Nobuki</creatorcontrib><creatorcontrib>Yamamoto, Yutaka</creatorcontrib><creatorcontrib>Ohno, Shinji</creatorcontrib><creatorcontrib>Takano, Toshimi</creatorcontrib><creatorcontrib>Morita, Satoshi</creatorcontrib><creatorcontrib>Tanaka-Mizuno, Sachiko</creatorcontrib><creatorcontrib>Toi, Masakazu</creatorcontrib><title>A randomized study comparing docetaxel/cyclophosphamide (TC), 5-fluorouracil/epirubicin/cyclophosphamide (FEC) followed by TC, and TC followed by FEC for patients with hormone receptor-positive HER2-negative primary breast cancer</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose Our primary objective was to determine the benefit/risk of anthracycline-free regimens by comparing docetaxel + cyclophosphamide (TC) alone, fluorouracil + epirubicin + cyclophosphamide (FEC) followed by TC, or TC followed by FEC as a primary treatment for patients with HR-positive, HER2-negative BC. Methods We randomized patients with stage I–III HR-positive HER2-negative, operable BC to receive either six cycles of TC (TC6), three cycles of FEC followed by three cycles of TC (FEC-TC), or three cycles of TC followed by three cycles of FEC (TC-FEC). The primary endpoint was the pathological response. Secondary endpoints included clinical response, type of surgical procedure, recurrence, death, and adverse events (by NCI-Common Terminology Criteria for Adverse Events v.3.0). We conducted all statistical analyses using SAS Version 9.2. Results We enrolled 195 patients and analyzed data from 193 as the intention-to-treat population. Pathological complete response rates were numerically higher in the TC6 group than in the other groups ( p  = 0.321). The breast conservation rate was significantly higher in the TC6 group (73%) than in the other groups (FEC-TC 51%, TC-FEC 45%, p  = 0.007). Adverse events with grade &gt; 3 were not common in the treatment groups ( p  = 0.569). The overall and distant disease-free survivals were similar among the groups with median follow-up of 5.80 years. Conclusions Despite similar long-term efficacy and safety profile, the higher breast conservation rate in the TC6 group suggests that preoperative chemotherapy without an anthracycline may benefit patients with HR-positive HER2-negative BC. Trial registration UMIN000003283 https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003873 .</description><subject>5-Fluorouracil</subject><subject>Adult</subject><subject>Aged</subject><subject>Anthracycline</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer therapies</subject><subject>Carcinoma, Ductal, Breast - drug therapy</subject><subject>Carcinoma, Ductal, Breast - pathology</subject><subject>Carcinoma, Lobular - drug therapy</subject><subject>Carcinoma, Lobular - pathology</subject><subject>Chemotherapy</subject><subject>Clinical Trial</subject><subject>Clinical trials</subject><subject>Creatinine</subject><subject>Cyclophosphamide</subject><subject>Cyclophosphamide - administration &amp; dosage</subject><subject>Docetaxel - administration &amp; dosage</subject><subject>Drug dosages</subject><subject>Edema</subject><subject>Epirubicin</subject><subject>Epirubicin - administration &amp; 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Masuda, Norikazu ; Sato, Nobuaki ; Higaki, Kenji ; Morimoto, Takashi ; Yanagita, Yasuhiro ; Mizutani, Makiko ; Ohtani, Shoichiro ; Kaneko, Koji ; Fujisawa, Tomomi ; Takahashi, Masato ; Kadoya, Takayuki ; Matsunami, Nobuki ; Yamamoto, Yutaka ; Ohno, Shinji ; Takano, Toshimi ; Morita, Satoshi ; Tanaka-Mizuno, Sachiko ; Toi, Masakazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-e9f61d02bf5f8dfb804465c0fec8de3e4e3ecfa9f049d1502029a231dcd0d9e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>5-Fluorouracil</topic><topic>Adult</topic><topic>Aged</topic><topic>Anthracycline</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer therapies</topic><topic>Carcinoma, Ductal, Breast - drug therapy</topic><topic>Carcinoma, Ductal, Breast - pathology</topic><topic>Carcinoma, Lobular - drug therapy</topic><topic>Carcinoma, Lobular - pathology</topic><topic>Chemotherapy</topic><topic>Clinical Trial</topic><topic>Clinical trials</topic><topic>Creatinine</topic><topic>Cyclophosphamide</topic><topic>Cyclophosphamide - administration &amp; dosage</topic><topic>Docetaxel - administration &amp; dosage</topic><topic>Drug dosages</topic><topic>Edema</topic><topic>Epirubicin</topic><topic>Epirubicin - administration &amp; dosage</topic><topic>ErbB-2 protein</topic><topic>Estrogens</topic><topic>Female</topic><topic>Fluorouracil - administration &amp; dosage</topic><topic>Follow-Up Studies</topic><topic>Granulocytes</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Neutropenia</topic><topic>Oncology</topic><topic>Patients</topic><topic>Peripheral neuropathy</topic><topic>Prognosis</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Receptors, Progesterone - metabolism</topic><topic>Registration</topic><topic>Statistical analysis</topic><topic>Survival Rate</topic><topic>Terminology</topic><topic>UMIN</topic><topic>UMIN000003283</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishiguro, Hiroshi</creatorcontrib><creatorcontrib>Masuda, Norikazu</creatorcontrib><creatorcontrib>Sato, Nobuaki</creatorcontrib><creatorcontrib>Higaki, Kenji</creatorcontrib><creatorcontrib>Morimoto, Takashi</creatorcontrib><creatorcontrib>Yanagita, Yasuhiro</creatorcontrib><creatorcontrib>Mizutani, Makiko</creatorcontrib><creatorcontrib>Ohtani, Shoichiro</creatorcontrib><creatorcontrib>Kaneko, Koji</creatorcontrib><creatorcontrib>Fujisawa, Tomomi</creatorcontrib><creatorcontrib>Takahashi, Masato</creatorcontrib><creatorcontrib>Kadoya, Takayuki</creatorcontrib><creatorcontrib>Matsunami, Nobuki</creatorcontrib><creatorcontrib>Yamamoto, Yutaka</creatorcontrib><creatorcontrib>Ohno, Shinji</creatorcontrib><creatorcontrib>Takano, Toshimi</creatorcontrib><creatorcontrib>Morita, Satoshi</creatorcontrib><creatorcontrib>Tanaka-Mizuno, Sachiko</creatorcontrib><creatorcontrib>Toi, Masakazu</creatorcontrib><collection>Springer Nature OA Free Journals</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>Health &amp; 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Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</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 China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishiguro, Hiroshi</au><au>Masuda, Norikazu</au><au>Sato, Nobuaki</au><au>Higaki, Kenji</au><au>Morimoto, Takashi</au><au>Yanagita, Yasuhiro</au><au>Mizutani, Makiko</au><au>Ohtani, Shoichiro</au><au>Kaneko, Koji</au><au>Fujisawa, Tomomi</au><au>Takahashi, Masato</au><au>Kadoya, Takayuki</au><au>Matsunami, Nobuki</au><au>Yamamoto, Yutaka</au><au>Ohno, Shinji</au><au>Takano, Toshimi</au><au>Morita, Satoshi</au><au>Tanaka-Mizuno, Sachiko</au><au>Toi, Masakazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A randomized study comparing docetaxel/cyclophosphamide (TC), 5-fluorouracil/epirubicin/cyclophosphamide (FEC) followed by TC, and TC followed by FEC for patients with hormone receptor-positive HER2-negative primary breast cancer</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2020-04-01</date><risdate>2020</risdate><volume>180</volume><issue>3</issue><spage>715</spage><epage>724</epage><pages>715-724</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><abstract>Purpose Our primary objective was to determine the benefit/risk of anthracycline-free regimens by comparing docetaxel + cyclophosphamide (TC) alone, fluorouracil + epirubicin + cyclophosphamide (FEC) followed by TC, or TC followed by FEC as a primary treatment for patients with HR-positive, HER2-negative BC. Methods We randomized patients with stage I–III HR-positive HER2-negative, operable BC to receive either six cycles of TC (TC6), three cycles of FEC followed by three cycles of TC (FEC-TC), or three cycles of TC followed by three cycles of FEC (TC-FEC). The primary endpoint was the pathological response. Secondary endpoints included clinical response, type of surgical procedure, recurrence, death, and adverse events (by NCI-Common Terminology Criteria for Adverse Events v.3.0). We conducted all statistical analyses using SAS Version 9.2. Results We enrolled 195 patients and analyzed data from 193 as the intention-to-treat population. Pathological complete response rates were numerically higher in the TC6 group than in the other groups ( p  = 0.321). The breast conservation rate was significantly higher in the TC6 group (73%) than in the other groups (FEC-TC 51%, TC-FEC 45%, p  = 0.007). Adverse events with grade &gt; 3 were not common in the treatment groups ( p  = 0.569). The overall and distant disease-free survivals were similar among the groups with median follow-up of 5.80 years. Conclusions Despite similar long-term efficacy and safety profile, the higher breast conservation rate in the TC6 group suggests that preoperative chemotherapy without an anthracycline may benefit patients with HR-positive HER2-negative BC. Trial registration UMIN000003283 https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000003873 .</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32170634</pmid><doi>10.1007/s10549-020-05590-w</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9859-5932</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0167-6806
ispartof Breast cancer research and treatment, 2020-04, Vol.180 (3), p.715-724
issn 0167-6806
1573-7217
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7103001
source MEDLINE; Springer Nature - Complete Springer Journals
subjects 5-Fluorouracil
Adult
Aged
Anthracycline
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Breast cancer
Breast Neoplasms - drug therapy
Breast Neoplasms - pathology
Cancer therapies
Carcinoma, Ductal, Breast - drug therapy
Carcinoma, Ductal, Breast - pathology
Carcinoma, Lobular - drug therapy
Carcinoma, Lobular - pathology
Chemotherapy
Clinical Trial
Clinical trials
Creatinine
Cyclophosphamide
Cyclophosphamide - administration & dosage
Docetaxel - administration & dosage
Drug dosages
Edema
Epirubicin
Epirubicin - administration & dosage
ErbB-2 protein
Estrogens
Female
Fluorouracil - administration & dosage
Follow-Up Studies
Granulocytes
Hemoglobin
Humans
Medical research
Medicine
Medicine & Public Health
Middle Aged
Neutropenia
Oncology
Patients
Peripheral neuropathy
Prognosis
Receptor, ErbB-2 - metabolism
Receptors, Estrogen - metabolism
Receptors, Progesterone - metabolism
Registration
Statistical analysis
Survival Rate
Terminology
UMIN
UMIN000003283
Young Adult
title A randomized study comparing docetaxel/cyclophosphamide (TC), 5-fluorouracil/epirubicin/cyclophosphamide (FEC) followed by TC, and TC followed by FEC for patients with hormone receptor-positive HER2-negative primary breast cancer
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