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Carboplatin plus taxanes are non-inferior to epirubicin plus cyclophosphamide followed by taxanes as adjuvant chemotherapy for early triple-negative breast cancer
Purpose Platinum plays an important role in the treatment of triple-negative breast cancer (TNBC) in neoadjuvant and metastatic settings. However, its role in an adjuvant setting remains unclear. Methods In this non-inferior randomized phase 2 trial, we randomly assigned 308 chemotherapy-naive patie...
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Published in: | Breast cancer research and treatment 2020-07, Vol.182 (1), p.67-77 |
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container_title | Breast cancer research and treatment |
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creator | Du, Feng Wang, Wenmiao Wang, Yongsheng Li, Ming Zhu, Anjie Wang, Jiayu Cai, Ruigang Ma, Fei Fan, Ying Li, Qing Zhang, Pin Todorovic, Vladimir Yuan, Peng Xu, Binghe |
description | Purpose
Platinum plays an important role in the treatment of triple-negative breast cancer (TNBC) in neoadjuvant and metastatic settings. However, its role in an adjuvant setting remains unclear.
Methods
In this non-inferior randomized phase 2 trial, we randomly assigned 308 chemotherapy-naive patients with histologically confirmed TNBC after primary surgery to receive either six cycles of TP (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
d1; carboplatin AUC = 5, day 1), or four cycles of EC (epirubicin: 90 mg/m
2
; cyclophosphamide: 600 mg/m
2
, day 1) followed by four cycles of T (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
, day 1). The primary end point was the disease-free survival (DFS) rate at 5 years. Both regimens were repeated every 3 weeks. The prognostic and predictive value of germline breast cancer gene mutations and programmed death ligand-1 (PD-L1) expression was evaluated.
Results
At a median follow-up of 66.9 months, the 5-year DFS rate was 85.8% in the EC-T arm, and 84.4% in the TP arm (p non-inferiority = 0.034,
p
log-rank = 0.712). The 5-year overall survival (OS) rate was 94.4% in the EC-T arm and 93.5% in the TP arm (
p
= 0.770). Patients in the TP arm showed better compliance and experienced significantly lower frequencies of G3/4 neutrocytopenia and G3/4 alopecia, but higher rates of G1–4 thrombocytopenia than those in the EC-T arm. Patients with PD-L1 expressing tumors showed significantly improved DFS and OS.
Conclusions
This study indicates that carboplatin plus taxanes could be a feasible adjuvant chemotherapy for patients with early TNBC who are cannot tolerate intensive chemotherapy with anthracycline. |
doi_str_mv | 10.1007/s10549-020-05648-9 |
format | article |
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Platinum plays an important role in the treatment of triple-negative breast cancer (TNBC) in neoadjuvant and metastatic settings. However, its role in an adjuvant setting remains unclear.
Methods
In this non-inferior randomized phase 2 trial, we randomly assigned 308 chemotherapy-naive patients with histologically confirmed TNBC after primary surgery to receive either six cycles of TP (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
d1; carboplatin AUC = 5, day 1), or four cycles of EC (epirubicin: 90 mg/m
2
; cyclophosphamide: 600 mg/m
2
, day 1) followed by four cycles of T (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
, day 1). The primary end point was the disease-free survival (DFS) rate at 5 years. Both regimens were repeated every 3 weeks. The prognostic and predictive value of germline breast cancer gene mutations and programmed death ligand-1 (PD-L1) expression was evaluated.
Results
At a median follow-up of 66.9 months, the 5-year DFS rate was 85.8% in the EC-T arm, and 84.4% in the TP arm (p non-inferiority = 0.034,
p
log-rank = 0.712). The 5-year overall survival (OS) rate was 94.4% in the EC-T arm and 93.5% in the TP arm (
p
= 0.770). Patients in the TP arm showed better compliance and experienced significantly lower frequencies of G3/4 neutrocytopenia and G3/4 alopecia, but higher rates of G1–4 thrombocytopenia than those in the EC-T arm. Patients with PD-L1 expressing tumors showed significantly improved DFS and OS.
Conclusions
This study indicates that carboplatin plus taxanes could be a feasible adjuvant chemotherapy for patients with early TNBC who are cannot tolerate intensive chemotherapy with anthracycline.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-020-05648-9</identifier><identifier>PMID: 32394350</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject><![CDATA[Adjuvant treatment ; Alopecia ; Anthracycline ; Anthracyclines ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Breast cancer ; Cancer ; Cancer research ; Carboplatin ; Carboplatin - administration & dosage ; Care and treatment ; Chemotherapy ; Chemotherapy, Adjuvant - mortality ; Clinical Trial ; Cyclophosphamide ; Cyclophosphamide - administration & dosage ; Docetaxel - administration & dosage ; Epirubicin ; Epirubicin - administration & dosage ; Equivalence Trials as Topic ; Female ; Follow-Up Studies ; Gene mutations ; Humans ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Middle Aged ; Oncology ; Paclitaxel ; Paclitaxel - administration & dosage ; Patients ; PD-L1 protein ; Platinum ; Prognosis ; Prospective Studies ; Rankings ; Surgery ; Survival ; Survival Rate ; Taxanes ; Thrombocytopenia ; Triple Negative Breast Neoplasms - drug therapy ; Triple Negative Breast Neoplasms - pathology ; Tumors]]></subject><ispartof>Breast cancer research and treatment, 2020-07, Vol.182 (1), p.67-77</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>COPYRIGHT 2020 Springer</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-5b0f6c329c3593be39b3a3c8535ba1a591cc776cdf99806db4ed8df2863d5a543</citedby><cites>FETCH-LOGICAL-c473t-5b0f6c329c3593be39b3a3c8535ba1a591cc776cdf99806db4ed8df2863d5a543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32394350$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Du, Feng</creatorcontrib><creatorcontrib>Wang, Wenmiao</creatorcontrib><creatorcontrib>Wang, Yongsheng</creatorcontrib><creatorcontrib>Li, Ming</creatorcontrib><creatorcontrib>Zhu, Anjie</creatorcontrib><creatorcontrib>Wang, Jiayu</creatorcontrib><creatorcontrib>Cai, Ruigang</creatorcontrib><creatorcontrib>Ma, Fei</creatorcontrib><creatorcontrib>Fan, Ying</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Zhang, Pin</creatorcontrib><creatorcontrib>Todorovic, Vladimir</creatorcontrib><creatorcontrib>Yuan, Peng</creatorcontrib><creatorcontrib>Xu, Binghe</creatorcontrib><title>Carboplatin plus taxanes are non-inferior to epirubicin plus cyclophosphamide followed by taxanes as adjuvant chemotherapy for early triple-negative breast cancer</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose
Platinum plays an important role in the treatment of triple-negative breast cancer (TNBC) in neoadjuvant and metastatic settings. However, its role in an adjuvant setting remains unclear.
Methods
In this non-inferior randomized phase 2 trial, we randomly assigned 308 chemotherapy-naive patients with histologically confirmed TNBC after primary surgery to receive either six cycles of TP (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
d1; carboplatin AUC = 5, day 1), or four cycles of EC (epirubicin: 90 mg/m
2
; cyclophosphamide: 600 mg/m
2
, day 1) followed by four cycles of T (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
, day 1). The primary end point was the disease-free survival (DFS) rate at 5 years. Both regimens were repeated every 3 weeks. The prognostic and predictive value of germline breast cancer gene mutations and programmed death ligand-1 (PD-L1) expression was evaluated.
Results
At a median follow-up of 66.9 months, the 5-year DFS rate was 85.8% in the EC-T arm, and 84.4% in the TP arm (p non-inferiority = 0.034,
p
log-rank = 0.712). The 5-year overall survival (OS) rate was 94.4% in the EC-T arm and 93.5% in the TP arm (
p
= 0.770). Patients in the TP arm showed better compliance and experienced significantly lower frequencies of G3/4 neutrocytopenia and G3/4 alopecia, but higher rates of G1–4 thrombocytopenia than those in the EC-T arm. Patients with PD-L1 expressing tumors showed significantly improved DFS and OS.
Conclusions
This study indicates that carboplatin plus taxanes could be a feasible adjuvant chemotherapy for patients with early TNBC who are cannot tolerate intensive chemotherapy with anthracycline.</description><subject>Adjuvant treatment</subject><subject>Alopecia</subject><subject>Anthracycline</subject><subject>Anthracyclines</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Cancer research</subject><subject>Carboplatin</subject><subject>Carboplatin - administration & dosage</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant - mortality</subject><subject>Clinical Trial</subject><subject>Cyclophosphamide</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Docetaxel - administration & dosage</subject><subject>Epirubicin</subject><subject>Epirubicin - administration & dosage</subject><subject>Equivalence Trials as Topic</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gene mutations</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Paclitaxel</subject><subject>Paclitaxel - administration & dosage</subject><subject>Patients</subject><subject>PD-L1 protein</subject><subject>Platinum</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Rankings</subject><subject>Surgery</subject><subject>Survival</subject><subject>Survival Rate</subject><subject>Taxanes</subject><subject>Thrombocytopenia</subject><subject>Triple Negative Breast Neoplasms - drug therapy</subject><subject>Triple Negative Breast Neoplasms - pathology</subject><subject>Tumors</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kt-K3CAUxkNp6U63fYFeFKGwd241xiReLkP_wUJv2mtRczJxMJqq2e68Tp-0bme304VSFAT9fd_xHL6qek3JJSWke5co4Y3ApCaY8LbpsXhSbSjvGO5q2j2tNoS2HW570p5VL1LaE0JER8Tz6ozVTDSMk031c6uiDotT2Xq0uDWhrG6Vh4RUBOSDx9aPEG2IKAcEi42rtuaBNQfjwjKFtExqtgOgMTgXfsCA9OFkVPawX2-Uz8hMMIc8QVTLocARgYquoNEuDrCHXfnHDSAdQaVCK28gvqyejcoleHV_nlffPrz_uv2Er798_Ly9usam6VjGXJOxNawWhnHBNDChmWKm54xrRRUX1Jiua80wClFGMugGhn4Y675lA1e8YefV26PvEsP3FVKW-7BGX0rKuiGip5w0_YnaKQeyDCfkqMxsk5FXbc170daUF-ryH1RZA8zWBA-jLfePBBd_CSZQLk8puDXb4NNjsD6CJoaUIoxyiXZW8SApkXexkMdYyBIL-TsWUhTRm_vWVj3D8EfykIMCsCOQypPfQTz1_h_bX3a2xQ8</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Du, Feng</creator><creator>Wang, Wenmiao</creator><creator>Wang, Yongsheng</creator><creator>Li, Ming</creator><creator>Zhu, Anjie</creator><creator>Wang, Jiayu</creator><creator>Cai, Ruigang</creator><creator>Ma, Fei</creator><creator>Fan, Ying</creator><creator>Li, Qing</creator><creator>Zhang, Pin</creator><creator>Todorovic, Vladimir</creator><creator>Yuan, Peng</creator><creator>Xu, Binghe</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><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></search><sort><creationdate>20200701</creationdate><title>Carboplatin plus taxanes are non-inferior to epirubicin plus cyclophosphamide followed by taxanes as adjuvant chemotherapy for early triple-negative breast cancer</title><author>Du, Feng ; Wang, Wenmiao ; Wang, Yongsheng ; Li, Ming ; Zhu, Anjie ; Wang, Jiayu ; Cai, Ruigang ; Ma, Fei ; Fan, Ying ; Li, Qing ; Zhang, Pin ; Todorovic, Vladimir ; Yuan, Peng ; Xu, Binghe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-5b0f6c329c3593be39b3a3c8535ba1a591cc776cdf99806db4ed8df2863d5a543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adjuvant treatment</topic><topic>Alopecia</topic><topic>Anthracycline</topic><topic>Anthracyclines</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Cancer research</topic><topic>Carboplatin</topic><topic>Carboplatin - administration & dosage</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Chemotherapy, Adjuvant - mortality</topic><topic>Clinical Trial</topic><topic>Cyclophosphamide</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Docetaxel - administration & dosage</topic><topic>Epirubicin</topic><topic>Epirubicin - administration & dosage</topic><topic>Equivalence Trials as Topic</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gene mutations</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Paclitaxel</topic><topic>Paclitaxel - administration & dosage</topic><topic>Patients</topic><topic>PD-L1 protein</topic><topic>Platinum</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Rankings</topic><topic>Surgery</topic><topic>Survival</topic><topic>Survival Rate</topic><topic>Taxanes</topic><topic>Thrombocytopenia</topic><topic>Triple Negative Breast Neoplasms - drug therapy</topic><topic>Triple Negative Breast Neoplasms - pathology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Du, Feng</creatorcontrib><creatorcontrib>Wang, Wenmiao</creatorcontrib><creatorcontrib>Wang, Yongsheng</creatorcontrib><creatorcontrib>Li, Ming</creatorcontrib><creatorcontrib>Zhu, Anjie</creatorcontrib><creatorcontrib>Wang, Jiayu</creatorcontrib><creatorcontrib>Cai, Ruigang</creatorcontrib><creatorcontrib>Ma, Fei</creatorcontrib><creatorcontrib>Fan, Ying</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Zhang, Pin</creatorcontrib><creatorcontrib>Todorovic, Vladimir</creatorcontrib><creatorcontrib>Yuan, Peng</creatorcontrib><creatorcontrib>Xu, Binghe</creatorcontrib><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)</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><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Du, Feng</au><au>Wang, Wenmiao</au><au>Wang, Yongsheng</au><au>Li, Ming</au><au>Zhu, Anjie</au><au>Wang, Jiayu</au><au>Cai, Ruigang</au><au>Ma, Fei</au><au>Fan, Ying</au><au>Li, Qing</au><au>Zhang, Pin</au><au>Todorovic, Vladimir</au><au>Yuan, Peng</au><au>Xu, Binghe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carboplatin plus taxanes are non-inferior to epirubicin plus cyclophosphamide followed by taxanes as adjuvant chemotherapy for early triple-negative breast cancer</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2020-07-01</date><risdate>2020</risdate><volume>182</volume><issue>1</issue><spage>67</spage><epage>77</epage><pages>67-77</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><abstract>Purpose
Platinum plays an important role in the treatment of triple-negative breast cancer (TNBC) in neoadjuvant and metastatic settings. However, its role in an adjuvant setting remains unclear.
Methods
In this non-inferior randomized phase 2 trial, we randomly assigned 308 chemotherapy-naive patients with histologically confirmed TNBC after primary surgery to receive either six cycles of TP (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
d1; carboplatin AUC = 5, day 1), or four cycles of EC (epirubicin: 90 mg/m
2
; cyclophosphamide: 600 mg/m
2
, day 1) followed by four cycles of T (docetaxel: 75 mg/m
2
or paclitaxel 175 mg/m
2
, day 1). The primary end point was the disease-free survival (DFS) rate at 5 years. Both regimens were repeated every 3 weeks. The prognostic and predictive value of germline breast cancer gene mutations and programmed death ligand-1 (PD-L1) expression was evaluated.
Results
At a median follow-up of 66.9 months, the 5-year DFS rate was 85.8% in the EC-T arm, and 84.4% in the TP arm (p non-inferiority = 0.034,
p
log-rank = 0.712). The 5-year overall survival (OS) rate was 94.4% in the EC-T arm and 93.5% in the TP arm (
p
= 0.770). Patients in the TP arm showed better compliance and experienced significantly lower frequencies of G3/4 neutrocytopenia and G3/4 alopecia, but higher rates of G1–4 thrombocytopenia than those in the EC-T arm. Patients with PD-L1 expressing tumors showed significantly improved DFS and OS.
Conclusions
This study indicates that carboplatin plus taxanes could be a feasible adjuvant chemotherapy for patients with early TNBC who are cannot tolerate intensive chemotherapy with anthracycline.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32394350</pmid><doi>10.1007/s10549-020-05648-9</doi><tpages>11</tpages></addata></record> |
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subjects | Adjuvant treatment Alopecia Anthracycline Anthracyclines Antineoplastic Combined Chemotherapy Protocols - therapeutic use Breast cancer Cancer Cancer research Carboplatin Carboplatin - administration & dosage Care and treatment Chemotherapy Chemotherapy, Adjuvant - mortality Clinical Trial Cyclophosphamide Cyclophosphamide - administration & dosage Docetaxel - administration & dosage Epirubicin Epirubicin - administration & dosage Equivalence Trials as Topic Female Follow-Up Studies Gene mutations Humans Medicine Medicine & Public Health Metastases Metastasis Middle Aged Oncology Paclitaxel Paclitaxel - administration & dosage Patients PD-L1 protein Platinum Prognosis Prospective Studies Rankings Surgery Survival Survival Rate Taxanes Thrombocytopenia Triple Negative Breast Neoplasms - drug therapy Triple Negative Breast Neoplasms - pathology Tumors |
title | Carboplatin plus taxanes are non-inferior to epirubicin plus cyclophosphamide followed by taxanes as adjuvant chemotherapy for early triple-negative breast cancer |
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