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Multicenter analysis of neoadjuvant docetaxel, carboplatin, and trastuzumab in HER2-positive breast cancer
Purpose In an era where neoadjuvant dual blockade is emerging as the standard of care for early and locally advanced HER2-positive breast cancer, we aimed to identify predictors of response to single-blockade chemotherapy. Methods This retrospective analysis reviewed all the incident stage I–III HER...
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Published in: | Breast cancer research and treatment 2017-02, Vol.162 (1), p.181-189 |
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creator | Echavarria, Isabel Granja, Mónica Bueno, Coralia Lopez-Tarruella, Sara Peinado, Paloma Sotelo, Miguel Jerez, Yolanda Moreno, Fernando Torres, Gabriela Lobo, Miriam Marquez-Rodas, Ivan Del Monte-Millan, Maria Martín, Miguel García-Saenz, Jose Angel |
description | Purpose
In an era where neoadjuvant dual blockade is emerging as the standard of care for early and locally advanced HER2-positive breast cancer, we aimed to identify predictors of response to single-blockade chemotherapy.
Methods
This retrospective analysis reviewed all the incident stage I–III HER2-positive breast cancer patients who received neoadjuvant docetaxel, carboplatin, and trastuzumab (TCH) in three institutions. pCR was defined as the absence of invasive tumor in breast and axillary nodes (ypT0/isypN0).
Results
From 2008 to 2015, 84 patients receiving neoadjuvant TCH were identified within our institutions. The mean age at diagnosis was 51.8 years. 59.5% of the patients were hormone receptor (HR) positive, lymph node involvement occurred in 67.9%, and clinical distribution was 2.4, 65.5, and 32.1% for stage I, II, and III, respectively. pCR rate was 47.6%; there was a significantly lower response in HR-positive patients compared to HR-negative ones (34 vs 67.6%,
p
= 0.005). pCR rate was associated with tumor size, whereas differences did not reach significance either for stage or for nodal status. Multivariate analysis found that only HR status was associated with response (
p
= 0.003). At a median follow-up of 31.7 months, disease-free survival, distant disease-free survival, and overall survival were 78.6, 85.7, and 94%, respectively. Breast-conserving surgery was performed in 44% of the patients. Overall, TCH was well tolerated, with low rates of grade 3–4 adverse events, and neither late toxicities nor cardiac dysfunctions were reported.
Conclusions
Neoadjuvant TCH, an anthracycline-free single-blockade regimen, achieved a pCR of 47.6%. Further molecular analyses are required in order to identify stronger predictive markers of pCR and thus for an accurate selection of patients who do not benefit from dual blockade. |
doi_str_mv | 10.1007/s10549-016-4098-z |
format | article |
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In an era where neoadjuvant dual blockade is emerging as the standard of care for early and locally advanced HER2-positive breast cancer, we aimed to identify predictors of response to single-blockade chemotherapy.
Methods
This retrospective analysis reviewed all the incident stage I–III HER2-positive breast cancer patients who received neoadjuvant docetaxel, carboplatin, and trastuzumab (TCH) in three institutions. pCR was defined as the absence of invasive tumor in breast and axillary nodes (ypT0/isypN0).
Results
From 2008 to 2015, 84 patients receiving neoadjuvant TCH were identified within our institutions. The mean age at diagnosis was 51.8 years. 59.5% of the patients were hormone receptor (HR) positive, lymph node involvement occurred in 67.9%, and clinical distribution was 2.4, 65.5, and 32.1% for stage I, II, and III, respectively. pCR rate was 47.6%; there was a significantly lower response in HR-positive patients compared to HR-negative ones (34 vs 67.6%,
p
= 0.005). pCR rate was associated with tumor size, whereas differences did not reach significance either for stage or for nodal status. Multivariate analysis found that only HR status was associated with response (
p
= 0.003). At a median follow-up of 31.7 months, disease-free survival, distant disease-free survival, and overall survival were 78.6, 85.7, and 94%, respectively. Breast-conserving surgery was performed in 44% of the patients. Overall, TCH was well tolerated, with low rates of grade 3–4 adverse events, and neither late toxicities nor cardiac dysfunctions were reported.
Conclusions
Neoadjuvant TCH, an anthracycline-free single-blockade regimen, achieved a pCR of 47.6%. Further molecular analyses are required in order to identify stronger predictive markers of pCR and thus for an accurate selection of patients who do not benefit from dual blockade.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-016-4098-z</identifier><identifier>PMID: 28040858</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adult ; Aged ; Analysis ; Anthracyclines ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biomarkers, Tumor ; Breast cancer ; Breast Neoplasms - diagnosis ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Breast Neoplasms - mortality ; Brief Report ; Cancer ; Cancer research ; Cancer therapies ; Carboplatin ; Carboplatin - administration & dosage ; Chemotherapy ; Epidermal growth factor ; Female ; Humans ; Kaplan-Meier Estimate ; Lumpectomy ; Medicine ; Medicine & Public Health ; Middle Aged ; Neoadjuvant Therapy ; Neoplasm Grading ; Neoplasm Staging ; Oncology ; Pertuzumab ; Receptor, ErbB-2 - metabolism ; Taxoids - administration & dosage ; Trastuzumab - administration & dosage ; Treatment Outcome ; Young Adult</subject><ispartof>Breast cancer research and treatment, 2017-02, Vol.162 (1), p.181-189</ispartof><rights>Springer Science+Business Media New York 2016</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Breast Cancer Research and Treatment is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-128ceec0bd535942428adad4911aaa8e3b316a83fc92372282261f4c11e1a1ed3</citedby><cites>FETCH-LOGICAL-c470t-128ceec0bd535942428adad4911aaa8e3b316a83fc92372282261f4c11e1a1ed3</cites><orcidid>0000-0002-1156-7681</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28040858$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Echavarria, Isabel</creatorcontrib><creatorcontrib>Granja, Mónica</creatorcontrib><creatorcontrib>Bueno, Coralia</creatorcontrib><creatorcontrib>Lopez-Tarruella, Sara</creatorcontrib><creatorcontrib>Peinado, Paloma</creatorcontrib><creatorcontrib>Sotelo, Miguel</creatorcontrib><creatorcontrib>Jerez, Yolanda</creatorcontrib><creatorcontrib>Moreno, Fernando</creatorcontrib><creatorcontrib>Torres, Gabriela</creatorcontrib><creatorcontrib>Lobo, Miriam</creatorcontrib><creatorcontrib>Marquez-Rodas, Ivan</creatorcontrib><creatorcontrib>Del Monte-Millan, Maria</creatorcontrib><creatorcontrib>Martín, Miguel</creatorcontrib><creatorcontrib>García-Saenz, Jose Angel</creatorcontrib><title>Multicenter analysis of neoadjuvant docetaxel, carboplatin, and trastuzumab in HER2-positive breast cancer</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose
In an era where neoadjuvant dual blockade is emerging as the standard of care for early and locally advanced HER2-positive breast cancer, we aimed to identify predictors of response to single-blockade chemotherapy.
Methods
This retrospective analysis reviewed all the incident stage I–III HER2-positive breast cancer patients who received neoadjuvant docetaxel, carboplatin, and trastuzumab (TCH) in three institutions. pCR was defined as the absence of invasive tumor in breast and axillary nodes (ypT0/isypN0).
Results
From 2008 to 2015, 84 patients receiving neoadjuvant TCH were identified within our institutions. The mean age at diagnosis was 51.8 years. 59.5% of the patients were hormone receptor (HR) positive, lymph node involvement occurred in 67.9%, and clinical distribution was 2.4, 65.5, and 32.1% for stage I, II, and III, respectively. pCR rate was 47.6%; there was a significantly lower response in HR-positive patients compared to HR-negative ones (34 vs 67.6%,
p
= 0.005). pCR rate was associated with tumor size, whereas differences did not reach significance either for stage or for nodal status. Multivariate analysis found that only HR status was associated with response (
p
= 0.003). At a median follow-up of 31.7 months, disease-free survival, distant disease-free survival, and overall survival were 78.6, 85.7, and 94%, respectively. Breast-conserving surgery was performed in 44% of the patients. Overall, TCH was well tolerated, with low rates of grade 3–4 adverse events, and neither late toxicities nor cardiac dysfunctions were reported.
Conclusions
Neoadjuvant TCH, an anthracycline-free single-blockade regimen, achieved a pCR of 47.6%. Further molecular analyses are required in order to identify stronger predictive markers of pCR and thus for an accurate selection of patients who do not benefit from dual blockade.</description><subject>Adult</subject><subject>Aged</subject><subject>Analysis</subject><subject>Anthracyclines</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biomarkers, Tumor</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - diagnosis</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - mortality</subject><subject>Brief Report</subject><subject>Cancer</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Carboplatin</subject><subject>Carboplatin - administration & dosage</subject><subject>Chemotherapy</subject><subject>Epidermal growth factor</subject><subject>Female</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lumpectomy</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>Neoplasm Grading</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Pertuzumab</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Taxoids - administration & dosage</subject><subject>Trastuzumab - administration & dosage</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1klFrFDEUhYModq3-AF9kQBAfOjXJTGaSx1JqK1QE0edwJ3OnzZJJ1iRT7P56s2yrrSh5COR858DJvYS8ZvSYUdp_SIyKVtWUdXVLlay3T8iKib6pe876p2RVhL7uJO0OyIuU1pRS1VP1nBxwSVsqhVyR9efFZWvQZ4wVeHC3yaYqTJXHAON6uQGfqzEYzPAT3VFlIA5h4yBbf1T4scoRUl62ywxDZX11cfaV15uQbLY3WA0Ri1pM3mB8SZ5N4BK-ursPyfePZ99OL-rLL-efTk8ua9P2NNeMS4No6DCKRqiWt1zCCGOrGAMAic3QsA5kMxnFm55zyXnHptYwhgwYjs0heb_P3cTwY8GU9WyTQeegdFqSZlK0vVKUqYK-_QtdhyWWX9hRneBCNY34Q12BQ239FEppswvVJ0IwypXkbaGO_0GVM-JsTfA42fL-yPDugeEaweXrFNySbfDpMcj2oIkhpYiT3kQ7Q7zVjOrdIuj9Iugyb71bBL0tnjd3zZZhxvG3437yBeB7IBXJX2F8UP2_qb8ABZy8Yw</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Echavarria, Isabel</creator><creator>Granja, Mónica</creator><creator>Bueno, Coralia</creator><creator>Lopez-Tarruella, Sara</creator><creator>Peinado, Paloma</creator><creator>Sotelo, Miguel</creator><creator>Jerez, Yolanda</creator><creator>Moreno, Fernando</creator><creator>Torres, Gabriela</creator><creator>Lobo, Miriam</creator><creator>Marquez-Rodas, Ivan</creator><creator>Del Monte-Millan, Maria</creator><creator>Martín, Miguel</creator><creator>García-Saenz, Jose Angel</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><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1156-7681</orcidid></search><sort><creationdate>20170201</creationdate><title>Multicenter analysis of neoadjuvant docetaxel, carboplatin, and trastuzumab in HER2-positive breast cancer</title><author>Echavarria, Isabel ; Granja, Mónica ; Bueno, Coralia ; Lopez-Tarruella, Sara ; Peinado, Paloma ; Sotelo, Miguel ; Jerez, Yolanda ; Moreno, Fernando ; Torres, Gabriela ; Lobo, Miriam ; Marquez-Rodas, Ivan ; Del Monte-Millan, Maria ; Martín, Miguel ; García-Saenz, Jose Angel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-128ceec0bd535942428adad4911aaa8e3b316a83fc92372282261f4c11e1a1ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Analysis</topic><topic>Anthracyclines</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biomarkers, Tumor</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - diagnosis</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - mortality</topic><topic>Brief Report</topic><topic>Cancer</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Carboplatin</topic><topic>Carboplatin - administration & dosage</topic><topic>Chemotherapy</topic><topic>Epidermal growth factor</topic><topic>Female</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lumpectomy</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>Neoplasm Grading</topic><topic>Neoplasm Staging</topic><topic>Oncology</topic><topic>Pertuzumab</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Taxoids - administration & dosage</topic><topic>Trastuzumab - administration & dosage</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Echavarria, Isabel</creatorcontrib><creatorcontrib>Granja, Mónica</creatorcontrib><creatorcontrib>Bueno, Coralia</creatorcontrib><creatorcontrib>Lopez-Tarruella, Sara</creatorcontrib><creatorcontrib>Peinado, Paloma</creatorcontrib><creatorcontrib>Sotelo, Miguel</creatorcontrib><creatorcontrib>Jerez, Yolanda</creatorcontrib><creatorcontrib>Moreno, Fernando</creatorcontrib><creatorcontrib>Torres, Gabriela</creatorcontrib><creatorcontrib>Lobo, Miriam</creatorcontrib><creatorcontrib>Marquez-Rodas, Ivan</creatorcontrib><creatorcontrib>Del Monte-Millan, Maria</creatorcontrib><creatorcontrib>Martín, Miguel</creatorcontrib><creatorcontrib>García-Saenz, Jose Angel</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</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>MEDLINE - Academic</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Echavarria, Isabel</au><au>Granja, Mónica</au><au>Bueno, Coralia</au><au>Lopez-Tarruella, Sara</au><au>Peinado, Paloma</au><au>Sotelo, Miguel</au><au>Jerez, Yolanda</au><au>Moreno, Fernando</au><au>Torres, Gabriela</au><au>Lobo, Miriam</au><au>Marquez-Rodas, Ivan</au><au>Del Monte-Millan, Maria</au><au>Martín, Miguel</au><au>García-Saenz, Jose Angel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multicenter analysis of neoadjuvant docetaxel, carboplatin, and trastuzumab in HER2-positive breast cancer</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>162</volume><issue>1</issue><spage>181</spage><epage>189</epage><pages>181-189</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>Purpose
In an era where neoadjuvant dual blockade is emerging as the standard of care for early and locally advanced HER2-positive breast cancer, we aimed to identify predictors of response to single-blockade chemotherapy.
Methods
This retrospective analysis reviewed all the incident stage I–III HER2-positive breast cancer patients who received neoadjuvant docetaxel, carboplatin, and trastuzumab (TCH) in three institutions. pCR was defined as the absence of invasive tumor in breast and axillary nodes (ypT0/isypN0).
Results
From 2008 to 2015, 84 patients receiving neoadjuvant TCH were identified within our institutions. The mean age at diagnosis was 51.8 years. 59.5% of the patients were hormone receptor (HR) positive, lymph node involvement occurred in 67.9%, and clinical distribution was 2.4, 65.5, and 32.1% for stage I, II, and III, respectively. pCR rate was 47.6%; there was a significantly lower response in HR-positive patients compared to HR-negative ones (34 vs 67.6%,
p
= 0.005). pCR rate was associated with tumor size, whereas differences did not reach significance either for stage or for nodal status. Multivariate analysis found that only HR status was associated with response (
p
= 0.003). At a median follow-up of 31.7 months, disease-free survival, distant disease-free survival, and overall survival were 78.6, 85.7, and 94%, respectively. Breast-conserving surgery was performed in 44% of the patients. Overall, TCH was well tolerated, with low rates of grade 3–4 adverse events, and neither late toxicities nor cardiac dysfunctions were reported.
Conclusions
Neoadjuvant TCH, an anthracycline-free single-blockade regimen, achieved a pCR of 47.6%. Further molecular analyses are required in order to identify stronger predictive markers of pCR and thus for an accurate selection of patients who do not benefit from dual blockade.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>28040858</pmid><doi>10.1007/s10549-016-4098-z</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1156-7681</orcidid></addata></record> |
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source | Springer Nature |
subjects | Adult Aged Analysis Anthracyclines Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biomarkers, Tumor Breast cancer Breast Neoplasms - diagnosis Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Breast Neoplasms - mortality Brief Report Cancer Cancer research Cancer therapies Carboplatin Carboplatin - administration & dosage Chemotherapy Epidermal growth factor Female Humans Kaplan-Meier Estimate Lumpectomy Medicine Medicine & Public Health Middle Aged Neoadjuvant Therapy Neoplasm Grading Neoplasm Staging Oncology Pertuzumab Receptor, ErbB-2 - metabolism Taxoids - administration & dosage Trastuzumab - administration & dosage Treatment Outcome Young Adult |
title | Multicenter analysis of neoadjuvant docetaxel, carboplatin, and trastuzumab in HER2-positive breast cancer |
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