Analysis of the Pathologic Response to Primary Chemotherapy in Patients with Locally Advanced Breast Cancer Grouped According to Estrogen Receptor, Progesterone Receptor, and HER2 Status

Abstract Purpose In clinical practice, it is possible to classify breast tumors according to estrogen receptor (ER), progesterone receptor (PgR), and HER2 overexpression: ER negative, PgR negative, and HER2 overexpressing; ER negative, PgR negative, and HER2 negative; ER positive, PgR positive, and...

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Veröffentlicht in:Clinical breast cancer 2007-04, Vol.7 (7), p.559-564
Hauptverfasser: Fernández-Morales, Luis A, Seguí, Miquel A, Andreu, Xavier, Dalmau, Elsa, Sáez, Amparo, Pericay, Carles, Santos, Cristina, Montesinos, Jesús, Gallardo, Enrique, Arcusa, Angels, Saigí, Eugeni
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container_end_page 564
container_issue 7
container_start_page 559
container_title Clinical breast cancer
container_volume 7
creator Fernández-Morales, Luis A
Seguí, Miquel A
Andreu, Xavier
Dalmau, Elsa
Sáez, Amparo
Pericay, Carles
Santos, Cristina
Montesinos, Jesús
Gallardo, Enrique
Arcusa, Angels
Saigí, Eugeni
description Abstract Purpose In clinical practice, it is possible to classify breast tumors according to estrogen receptor (ER), progesterone receptor (PgR), and HER2 overexpression: ER negative, PgR negative, and HER2 overexpressing; ER negative, PgR negative, and HER2 negative; ER positive, PgR positive, and HER2 negative; ER positive, PgR positive, and HER2 overexpressing; and the less frequent remaining 4 combinations. The aim of this study was to determine the percentage of pathologic complete response (pCR) in patients with locally advanced breast cancer (LABC) treated with neoadjuvant or primary chemotherapy with anthracyclines and taxanes grouped according to ER, PgR, and HER2 status. Patients and Methods Patients with LABC treated with primary chemotherapy including anthracyclines and taxanes were grouped according to ER, PgR, and HER2 status; pCR rates were analyzed using the χ2 test; and correlations with a P value of ≤ 0.05 were considered statistically significant. Results A total of 103 patients were treated. Only 100 patients were included for the analysis of pCR. Eighteen patients exhibited pCR. The pCR rate for each subgroup was as follows: 39.1% (9 of 23) had ER-negative, PgR-negative, and HER2-negative disease ( P < 0.01); 35.7% (5 of 14) had ER-negative, PgR-negative, and HER2-overexpressing disease; 33.3% (3 of 9) had ER-positive, PgR-positive, and HER2-overexpressing disease; and 2.8% (1 of 36) had ER-positive, PgR-positive, and HER2-negative disease ( P < 0.01). Conclusion In patients with LABC, grouping breast tumors according to ER, PgR, and HER2 status can help predict pCR to primary chemotherapy.
doi_str_mv 10.3816/CBC.2007.n.012
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The aim of this study was to determine the percentage of pathologic complete response (pCR) in patients with locally advanced breast cancer (LABC) treated with neoadjuvant or primary chemotherapy with anthracyclines and taxanes grouped according to ER, PgR, and HER2 status. Patients and Methods Patients with LABC treated with primary chemotherapy including anthracyclines and taxanes were grouped according to ER, PgR, and HER2 status; pCR rates were analyzed using the χ2 test; and correlations with a P value of ≤ 0.05 were considered statistically significant. Results A total of 103 patients were treated. Only 100 patients were included for the analysis of pCR. Eighteen patients exhibited pCR. The pCR rate for each subgroup was as follows: 39.1% (9 of 23) had ER-negative, PgR-negative, and HER2-negative disease ( P &lt; 0.01); 35.7% (5 of 14) had ER-negative, PgR-negative, and HER2-overexpressing disease; 33.3% (3 of 9) had ER-positive, PgR-positive, and HER2-overexpressing disease; and 2.8% (1 of 36) had ER-positive, PgR-positive, and HER2-negative disease ( P &lt; 0.01). Conclusion In patients with LABC, grouping breast tumors according to ER, PgR, and HER2 status can help predict pCR to primary chemotherapy.</description><identifier>ISSN: 1526-8209</identifier><identifier>EISSN: 1938-0666</identifier><identifier>DOI: 10.3816/CBC.2007.n.012</identifier><identifier>PMID: 17509165</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Anthracyclines ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Basal-like subgroups ; Breast Neoplasms - drug therapy ; Breast Neoplasms - physiopathology ; Female ; Gene Expression - drug effects ; Genes, erbB-2 - drug effects ; Hematology, Oncology and Palliative Medicine ; Hormone receptor ; Humans ; Middle Aged ; Obstetrics and Gynecology ; Receptors, Estrogen - drug effects ; Receptors, Progesterone - drug effects ; Retrospective Studies ; Taxanes ; Trastuzumab ; Treatment Outcome</subject><ispartof>Clinical breast cancer, 2007-04, Vol.7 (7), p.559-564</ispartof><rights>Elsevier Inc.</rights><rights>2007 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-d6120f77f93818490ffc7512c575d9cd755b89580d0f15c31bc3ff2cdca453793</citedby><cites>FETCH-LOGICAL-c397t-d6120f77f93818490ffc7512c575d9cd755b89580d0f15c31bc3ff2cdca453793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.3816/CBC.2007.n.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17509165$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fernández-Morales, Luis A</creatorcontrib><creatorcontrib>Seguí, Miquel A</creatorcontrib><creatorcontrib>Andreu, Xavier</creatorcontrib><creatorcontrib>Dalmau, Elsa</creatorcontrib><creatorcontrib>Sáez, Amparo</creatorcontrib><creatorcontrib>Pericay, Carles</creatorcontrib><creatorcontrib>Santos, Cristina</creatorcontrib><creatorcontrib>Montesinos, Jesús</creatorcontrib><creatorcontrib>Gallardo, Enrique</creatorcontrib><creatorcontrib>Arcusa, Angels</creatorcontrib><creatorcontrib>Saigí, Eugeni</creatorcontrib><title>Analysis of the Pathologic Response to Primary Chemotherapy in Patients with Locally Advanced Breast Cancer Grouped According to Estrogen Receptor, Progesterone Receptor, and HER2 Status</title><title>Clinical breast cancer</title><addtitle>Clin Breast Cancer</addtitle><description>Abstract Purpose In clinical practice, it is possible to classify breast tumors according to estrogen receptor (ER), progesterone receptor (PgR), and HER2 overexpression: ER negative, PgR negative, and HER2 overexpressing; ER negative, PgR negative, and HER2 negative; ER positive, PgR positive, and HER2 negative; ER positive, PgR positive, and HER2 overexpressing; and the less frequent remaining 4 combinations. The aim of this study was to determine the percentage of pathologic complete response (pCR) in patients with locally advanced breast cancer (LABC) treated with neoadjuvant or primary chemotherapy with anthracyclines and taxanes grouped according to ER, PgR, and HER2 status. Patients and Methods Patients with LABC treated with primary chemotherapy including anthracyclines and taxanes were grouped according to ER, PgR, and HER2 status; pCR rates were analyzed using the χ2 test; and correlations with a P value of ≤ 0.05 were considered statistically significant. Results A total of 103 patients were treated. Only 100 patients were included for the analysis of pCR. Eighteen patients exhibited pCR. The pCR rate for each subgroup was as follows: 39.1% (9 of 23) had ER-negative, PgR-negative, and HER2-negative disease ( P &lt; 0.01); 35.7% (5 of 14) had ER-negative, PgR-negative, and HER2-overexpressing disease; 33.3% (3 of 9) had ER-positive, PgR-positive, and HER2-overexpressing disease; and 2.8% (1 of 36) had ER-positive, PgR-positive, and HER2-negative disease ( P &lt; 0.01). Conclusion In patients with LABC, grouping breast tumors according to ER, PgR, and HER2 status can help predict pCR to primary chemotherapy.</description><subject>Adult</subject><subject>Aged</subject><subject>Anthracyclines</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Basal-like subgroups</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - physiopathology</subject><subject>Female</subject><subject>Gene Expression - drug effects</subject><subject>Genes, erbB-2 - drug effects</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hormone receptor</subject><subject>Humans</subject><subject>Middle Aged</subject><subject>Obstetrics and Gynecology</subject><subject>Receptors, Estrogen - drug effects</subject><subject>Receptors, Progesterone - drug effects</subject><subject>Retrospective Studies</subject><subject>Taxanes</subject><subject>Trastuzumab</subject><subject>Treatment Outcome</subject><issn>1526-8209</issn><issn>1938-0666</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kl-P1CAUxRujcf_oq4-GJ5_sCHQo7YvJbDPumkziZlcT3wgDlxnWDlSga_rV9tNJM5NoTHwCbs49F86PonhD8KJqSP2hu-oWFGO-cAtM6LPinLRVU-K6rp_nPaN12VDcnhUXMT5gTOuK4JfFGeEMt6Rm58XTysl-ijYib1DaA7qVae97v7MK3UEcvIuAkke3wR5kmFC3h4PPuiCHCVk3yy24FNEvm_Zo45Xs-wmt9KN0CjS6CiBjQt18Cug6-HHI1ZVSPmjrdrPzOqbgd-DyOAVD8uF9HpYLMUHwDv4qS6fRzfqOovsk0xhfFS-M7CO8Pq2XxbdP66_dTbn5cv25W21KVbU8lbomFBvOTQ6GNMsWG6M4I1QxznSrNGds27SswRobwlRFtqoyhiqt5JJVvK0ui3dH3yH4n2O-lzjYqKDvpQM_RsExo9WSNVm4OApV8DEGMGI4piYIFjMtkWmJmZZwItPKDW9PzuP2APqP_IQnC5qjAPL7Hi0EEVWOOydrA6gktLf_9_74T6vqrbOZzw-YID74MWTyURARqcDifv4r81chhGO-pN-r355Lupw</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Fernández-Morales, Luis A</creator><creator>Seguí, Miquel A</creator><creator>Andreu, Xavier</creator><creator>Dalmau, Elsa</creator><creator>Sáez, Amparo</creator><creator>Pericay, Carles</creator><creator>Santos, Cristina</creator><creator>Montesinos, Jesús</creator><creator>Gallardo, Enrique</creator><creator>Arcusa, Angels</creator><creator>Saigí, Eugeni</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20070401</creationdate><title>Analysis of the Pathologic Response to Primary Chemotherapy in Patients with Locally Advanced Breast Cancer Grouped According to Estrogen Receptor, Progesterone Receptor, and HER2 Status</title><author>Fernández-Morales, Luis A ; Seguí, Miquel A ; Andreu, Xavier ; Dalmau, Elsa ; Sáez, Amparo ; Pericay, Carles ; Santos, Cristina ; Montesinos, Jesús ; Gallardo, Enrique ; Arcusa, Angels ; Saigí, Eugeni</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-d6120f77f93818490ffc7512c575d9cd755b89580d0f15c31bc3ff2cdca453793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anthracyclines</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Basal-like subgroups</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - physiopathology</topic><topic>Female</topic><topic>Gene Expression - drug effects</topic><topic>Genes, erbB-2 - drug effects</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hormone receptor</topic><topic>Humans</topic><topic>Middle Aged</topic><topic>Obstetrics and Gynecology</topic><topic>Receptors, Estrogen - drug effects</topic><topic>Receptors, Progesterone - drug effects</topic><topic>Retrospective Studies</topic><topic>Taxanes</topic><topic>Trastuzumab</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fernández-Morales, Luis A</creatorcontrib><creatorcontrib>Seguí, Miquel A</creatorcontrib><creatorcontrib>Andreu, Xavier</creatorcontrib><creatorcontrib>Dalmau, Elsa</creatorcontrib><creatorcontrib>Sáez, Amparo</creatorcontrib><creatorcontrib>Pericay, Carles</creatorcontrib><creatorcontrib>Santos, Cristina</creatorcontrib><creatorcontrib>Montesinos, Jesús</creatorcontrib><creatorcontrib>Gallardo, Enrique</creatorcontrib><creatorcontrib>Arcusa, Angels</creatorcontrib><creatorcontrib>Saigí, Eugeni</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical breast cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernández-Morales, Luis A</au><au>Seguí, Miquel A</au><au>Andreu, Xavier</au><au>Dalmau, Elsa</au><au>Sáez, Amparo</au><au>Pericay, Carles</au><au>Santos, Cristina</au><au>Montesinos, Jesús</au><au>Gallardo, Enrique</au><au>Arcusa, Angels</au><au>Saigí, Eugeni</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of the Pathologic Response to Primary Chemotherapy in Patients with Locally Advanced Breast Cancer Grouped According to Estrogen Receptor, Progesterone Receptor, and HER2 Status</atitle><jtitle>Clinical breast cancer</jtitle><addtitle>Clin Breast Cancer</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>7</volume><issue>7</issue><spage>559</spage><epage>564</epage><pages>559-564</pages><issn>1526-8209</issn><eissn>1938-0666</eissn><abstract>Abstract Purpose In clinical practice, it is possible to classify breast tumors according to estrogen receptor (ER), progesterone receptor (PgR), and HER2 overexpression: ER negative, PgR negative, and HER2 overexpressing; ER negative, PgR negative, and HER2 negative; ER positive, PgR positive, and HER2 negative; ER positive, PgR positive, and HER2 overexpressing; and the less frequent remaining 4 combinations. The aim of this study was to determine the percentage of pathologic complete response (pCR) in patients with locally advanced breast cancer (LABC) treated with neoadjuvant or primary chemotherapy with anthracyclines and taxanes grouped according to ER, PgR, and HER2 status. Patients and Methods Patients with LABC treated with primary chemotherapy including anthracyclines and taxanes were grouped according to ER, PgR, and HER2 status; pCR rates were analyzed using the χ2 test; and correlations with a P value of ≤ 0.05 were considered statistically significant. Results A total of 103 patients were treated. Only 100 patients were included for the analysis of pCR. Eighteen patients exhibited pCR. The pCR rate for each subgroup was as follows: 39.1% (9 of 23) had ER-negative, PgR-negative, and HER2-negative disease ( P &lt; 0.01); 35.7% (5 of 14) had ER-negative, PgR-negative, and HER2-overexpressing disease; 33.3% (3 of 9) had ER-positive, PgR-positive, and HER2-overexpressing disease; and 2.8% (1 of 36) had ER-positive, PgR-positive, and HER2-negative disease ( P &lt; 0.01). Conclusion In patients with LABC, grouping breast tumors according to ER, PgR, and HER2 status can help predict pCR to primary chemotherapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>17509165</pmid><doi>10.3816/CBC.2007.n.012</doi><tpages>6</tpages></addata></record>
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identifier ISSN: 1526-8209
ispartof Clinical breast cancer, 2007-04, Vol.7 (7), p.559-564
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1938-0666
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Adult
Aged
Anthracyclines
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Basal-like subgroups
Breast Neoplasms - drug therapy
Breast Neoplasms - physiopathology
Female
Gene Expression - drug effects
Genes, erbB-2 - drug effects
Hematology, Oncology and Palliative Medicine
Hormone receptor
Humans
Middle Aged
Obstetrics and Gynecology
Receptors, Estrogen - drug effects
Receptors, Progesterone - drug effects
Retrospective Studies
Taxanes
Trastuzumab
Treatment Outcome
title Analysis of the Pathologic Response to Primary Chemotherapy in Patients with Locally Advanced Breast Cancer Grouped According to Estrogen Receptor, Progesterone Receptor, and HER2 Status
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