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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
Main Authors: 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
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container_title Breast cancer research and treatment
container_volume 182
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
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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). 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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 &amp; 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 &amp; dosage</subject><subject>Docetaxel - administration &amp; dosage</subject><subject>Epirubicin</subject><subject>Epirubicin - administration &amp; 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 &amp; 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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 &amp; 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 &amp; 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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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