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 |
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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7103001</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2383878355</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-e9f61d02bf5f8dfb804465c0fec8de3e4e3ecfa9f049d1502029a231dcd0d9e13</originalsourceid><addsrcrecordid>eNp9Ul1rFDEUHUSx2-of8EECvlho3JvJfL4IZdlaoSDI-hwyyc1uysxkTGa6rv-3_8Nsd60WxIdwSe655xxuTpK8YfCBAZTzwCDPagopUMjzGuj2WTJjeclpmbLyeTIDVpS0qKA4SU5DuAWAuoT6ZXLCYx8Kns2S-0viZa9dZ3-iJmGc9I4o1w3S235NtFM4yh_YztVOtW7YuDBsZGc1kverxfkFyalpJ-fd5KWy7RwH66fGKtv_Y-BquTgnxrWt20apZkdWiwsStWN98hxx8e7JIEeL_RjI1o4bsnG-cz0SjwqH0Xk6uGBHe4fkevk1pT2u5cNt8LaTfkcajzKMRMleoX-VvDCyDfj6WM-Sb1fL1eKa3nz59HlxeUNVVmYjxdoUTEPamNxU2jQVZFmRKzCoKo0cs3iUkbWBrNYsj4tPa5lyppUGXSPjZ8nHA-8wNR1qFe172YqjJ-GkFU87vd2ItbsTJQMOsCd4dyTw7vuEYRS3cbd99CxSXvGqrHieR1R6QCnvQvBoHhUYiH00xCEaIjoUD9EQ2zj09m9vjyO_sxAB_AAIw_7z0f_R_g_tL1Eby4o</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2383878355</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><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</creator><creatorcontrib>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</creatorcontrib><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
.</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 & 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</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 > 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 & dosage</subject><subject>Docetaxel - administration & dosage</subject><subject>Drug dosages</subject><subject>Edema</subject><subject>Epirubicin</subject><subject>Epirubicin - administration & dosage</subject><subject>ErbB-2 protein</subject><subject>Estrogens</subject><subject>Female</subject><subject>Fluorouracil - administration & dosage</subject><subject>Follow-Up Studies</subject><subject>Granulocytes</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Neutropenia</subject><subject>Oncology</subject><subject>Patients</subject><subject>Peripheral neuropathy</subject><subject>Prognosis</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Receptors, Progesterone - metabolism</subject><subject>Registration</subject><subject>Statistical analysis</subject><subject>Survival Rate</subject><subject>Terminology</subject><subject>UMIN</subject><subject>UMIN000003283</subject><subject>Young Adult</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9Ul1rFDEUHUSx2-of8EECvlho3JvJfL4IZdlaoSDI-hwyyc1uysxkTGa6rv-3_8Nsd60WxIdwSe655xxuTpK8YfCBAZTzwCDPagopUMjzGuj2WTJjeclpmbLyeTIDVpS0qKA4SU5DuAWAuoT6ZXLCYx8Kns2S-0viZa9dZ3-iJmGc9I4o1w3S235NtFM4yh_YztVOtW7YuDBsZGc1kverxfkFyalpJ-fd5KWy7RwH66fGKtv_Y-BquTgnxrWt20apZkdWiwsStWN98hxx8e7JIEeL_RjI1o4bsnG-cz0SjwqH0Xk6uGBHe4fkevk1pT2u5cNt8LaTfkcajzKMRMleoX-VvDCyDfj6WM-Sb1fL1eKa3nz59HlxeUNVVmYjxdoUTEPamNxU2jQVZFmRKzCoKo0cs3iUkbWBrNYsj4tPa5lyppUGXSPjZ8nHA-8wNR1qFe172YqjJ-GkFU87vd2ItbsTJQMOsCd4dyTw7vuEYRS3cbd99CxSXvGqrHieR1R6QCnvQvBoHhUYiH00xCEaIjoUD9EQ2zj09m9vjyO_sxAB_AAIw_7z0f_R_g_tL1Eby4o</recordid><startdate>20200401</startdate><enddate>20200401</enddate><creator>Ishiguro, Hiroshi</creator><creator>Masuda, Norikazu</creator><creator>Sato, Nobuaki</creator><creator>Higaki, Kenji</creator><creator>Morimoto, Takashi</creator><creator>Yanagita, Yasuhiro</creator><creator>Mizutani, Makiko</creator><creator>Ohtani, Shoichiro</creator><creator>Kaneko, Koji</creator><creator>Fujisawa, Tomomi</creator><creator>Takahashi, Masato</creator><creator>Kadoya, Takayuki</creator><creator>Matsunami, Nobuki</creator><creator>Yamamoto, Yutaka</creator><creator>Ohno, Shinji</creator><creator>Takano, Toshimi</creator><creator>Morita, Satoshi</creator><creator>Tanaka-Mizuno, Sachiko</creator><creator>Toi, Masakazu</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</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>5PM</scope><orcidid>https://orcid.org/0000-0002-9859-5932</orcidid></search><sort><creationdate>20200401</creationdate><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><author>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</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 & dosage</topic><topic>Docetaxel - administration & dosage</topic><topic>Drug dosages</topic><topic>Edema</topic><topic>Epirubicin</topic><topic>Epirubicin - administration & dosage</topic><topic>ErbB-2 protein</topic><topic>Estrogens</topic><topic>Female</topic><topic>Fluorouracil - administration & 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 & 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 & 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 Edition)</collection><collection>ProQuest Central UK/Ireland</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>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 > 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> |
fulltext | fulltext |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T15%3A09%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20randomized%20study%20comparing%20docetaxel/cyclophosphamide%20(TC),%205-fluorouracil/epirubicin/cyclophosphamide%20(FEC)%20followed%20by%20TC,%20and%20TC%20followed%20by%20FEC%20for%20patients%20with%20hormone%20receptor-positive%20HER2-negative%20primary%20breast%20cancer&rft.jtitle=Breast%20cancer%20research%20and%20treatment&rft.au=Ishiguro,%20Hiroshi&rft.date=2020-04-01&rft.volume=180&rft.issue=3&rft.spage=715&rft.epage=724&rft.pages=715-724&rft.issn=0167-6806&rft.eissn=1573-7217&rft_id=info:doi/10.1007/s10549-020-05590-w&rft_dat=%3Cproquest_pubme%3E2383878355%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2383878355&rft_id=info:pmid/32170634&rfr_iscdi=true |