Neoadjuvant chemotherapy adaptation and serial MRI response monitoring in ER-positive HER2-negative breast cancer
Background: Changing the neoadjuvant chemotherapy regimen in insufficiently responding breast cancer is not a standard policy. We analysed a series of patients with ‘luminal’-type breast cancer in whom the second half of neoadjuvant chemotherapy was selected based on the response to the first half....
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Veröffentlicht in: | British journal of cancer 2013-12, Vol.109 (12), p.2965-2972 |
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creator | Rigter, L S Loo, C E Linn, S C Sonke, G S van Werkhoven, E Lips, E H Warnars, H A Doll, P K Bruining, A Mandjes, I A Vrancken Peeters, M J Wesseling, J Gilhuijs, K G Rodenhuis, S |
description | Background:
Changing the neoadjuvant chemotherapy regimen in insufficiently responding breast cancer is not a standard policy. We analysed a series of patients with ‘luminal’-type breast cancer in whom the second half of neoadjuvant chemotherapy was selected based on the response to the first half.
Methods:
Patients with oestrogen receptor-positive (ER+) human epidermal growth factor receptor 2-negative (HER2−) breast cancer received three courses of neoadjuvant dose-dense doxorubicin and cyclophosphamide (ddAC). Three further courses of ddAC were administered in case of a ‘favourable response’ on the interim magnetic resonance imaging (MRI) and a switch to docetaxel and capecitabine (DC) was made in case of an ‘unfavourable response’, using previously published response criteria. The efficacy of this approach was evaluated by tumour size reductions on serial contrast-enhanced MRI, pathologic response and relapse-free survival.
Results:
Two hundred and forty-six patients received three courses of ddAC. One hundred and sixty-four patients (67%) had a favourable response at the interim MRI, with a mean tumour size reduction of 31% after the first three courses and 34% after the second three courses. Patients with unfavourable responsive tumours had a mean tumour size reduction of 12% after three courses and received three courses of DC rather than ddAC. This led to a mean shrinkage of 27%.
Conclusion:
The tumour size reduction of initially less responsive tumours after treatment adaptation adds further evidence that a response-adapted strategy may enhance the efficacy of neoadjuvant chemotherapy. |
doi_str_mv | 10.1038/bjc.2013.661 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3859944</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3152271441</sourcerecordid><originalsourceid>FETCH-LOGICAL-c480t-9e52dbb7aca6bca0911df32f07e1d0e810abe6adcf466752b785c9d7d120b19b3</originalsourceid><addsrcrecordid>eNptkU2LUzEUhoMoTh3duZaAuPPWJPcj924EGaozMCoUXYeT5Nw2pU3uJGlh_r2preMIrsIhD-97OA8hrzmbc1b3H_TGzAXj9bzr-BMy420tKt4L-ZTMGGOyYoNgF-RFSpsyDqyXz8mFaHgzcNnPyN03DGA3-wP4TM0adyGvMcJ0T8HClCG74Cl4SxNGB1v6dXlDI6Yp-IR0F7zLITq_os7TxbKaQnLZHZBeL5ai8riC35OOCKnEgzcYX5JnI2wTvjq_l-Tn58WPq-vq9vuXm6tPt5VpeparAVthtZZgoNMG2MC5HWsxMoncMuw5A40dWDM2XSdboWXfmsFKywXTfND1Jfl4yp32eofWoM8RtmqKbgfxXgVw6t8f79ZqFQ6q7tthaJoS8PYcEMPdHlNWm7CPvuyseOlsWy4ZK9T7E2ViSCni-NDAmToKUkWQOgpSRVDB3zze6gH-Y6QA784AJAPbMZajufSX61nTdp0oXHXi0nQUgPHRdv8r_gVtZ6qD</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1466551700</pqid></control><display><type>article</type><title>Neoadjuvant chemotherapy adaptation and serial MRI response monitoring in ER-positive HER2-negative breast cancer</title><source>MEDLINE</source><source>Nature</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>SpringerLink Journals - AutoHoldings</source><creator>Rigter, L S ; Loo, C E ; Linn, S C ; Sonke, G S ; van Werkhoven, E ; Lips, E H ; Warnars, H A ; Doll, P K ; Bruining, A ; Mandjes, I A ; Vrancken Peeters, M J ; Wesseling, J ; Gilhuijs, K G ; Rodenhuis, S</creator><creatorcontrib>Rigter, L S ; Loo, C E ; Linn, S C ; Sonke, G S ; van Werkhoven, E ; Lips, E H ; Warnars, H A ; Doll, P K ; Bruining, A ; Mandjes, I A ; Vrancken Peeters, M J ; Wesseling, J ; Gilhuijs, K G ; Rodenhuis, S</creatorcontrib><description>Background:
Changing the neoadjuvant chemotherapy regimen in insufficiently responding breast cancer is not a standard policy. We analysed a series of patients with ‘luminal’-type breast cancer in whom the second half of neoadjuvant chemotherapy was selected based on the response to the first half.
Methods:
Patients with oestrogen receptor-positive (ER+) human epidermal growth factor receptor 2-negative (HER2−) breast cancer received three courses of neoadjuvant dose-dense doxorubicin and cyclophosphamide (ddAC). Three further courses of ddAC were administered in case of a ‘favourable response’ on the interim magnetic resonance imaging (MRI) and a switch to docetaxel and capecitabine (DC) was made in case of an ‘unfavourable response’, using previously published response criteria. The efficacy of this approach was evaluated by tumour size reductions on serial contrast-enhanced MRI, pathologic response and relapse-free survival.
Results:
Two hundred and forty-six patients received three courses of ddAC. One hundred and sixty-four patients (67%) had a favourable response at the interim MRI, with a mean tumour size reduction of 31% after the first three courses and 34% after the second three courses. Patients with unfavourable responsive tumours had a mean tumour size reduction of 12% after three courses and received three courses of DC rather than ddAC. This led to a mean shrinkage of 27%.
Conclusion:
The tumour size reduction of initially less responsive tumours after treatment adaptation adds further evidence that a response-adapted strategy may enhance the efficacy of neoadjuvant chemotherapy.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.2013.661</identifier><identifier>PMID: 24149178</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject><![CDATA[692/699/67/1059/99 ; 692/699/67/1347 ; 692/700/1421/1628 ; Adaptation ; Adolescent ; Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Cancer Research ; Cancer therapies ; Capecitabine ; Chemotherapy ; Chemotherapy, Adjuvant ; Clinical Study ; Clinical trials ; Cyclophosphamide - administration & dosage ; Deoxycytidine - administration & dosage ; Deoxycytidine - analogs & derivatives ; Doxorubicin - administration & dosage ; Drug Resistance ; Epidemiology ; Epidermal growth factor ; Female ; Filgrastim ; Fluorouracil - administration & dosage ; Fluorouracil - analogs & derivatives ; Granulocyte Colony-Stimulating Factor - administration & dosage ; Gynecology. Andrology. Obstetrics ; Humans ; Immunohistochemistry ; Magnetic Resonance Imaging ; Mammary gland diseases ; Medical sciences ; Middle Aged ; Molecular Medicine ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Neoadjuvant Therapy ; Oncology ; Receptor, ErbB-2 - biosynthesis ; Receptors, Estrogen - biosynthesis ; Recombinant Proteins - administration & dosage ; Survival Analysis ; Taxoids - administration & dosage ; Tumors ; Young Adult]]></subject><ispartof>British journal of cancer, 2013-12, Vol.109 (12), p.2965-2972</ispartof><rights>The Author(s) 2013</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Dec 10, 2013</rights><rights>Copyright © 2013 Cancer Research UK 2013 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-9e52dbb7aca6bca0911df32f07e1d0e810abe6adcf466752b785c9d7d120b19b3</citedby><cites>FETCH-LOGICAL-c480t-9e52dbb7aca6bca0911df32f07e1d0e810abe6adcf466752b785c9d7d120b19b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859944/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859944/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28045662$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24149178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rigter, L S</creatorcontrib><creatorcontrib>Loo, C E</creatorcontrib><creatorcontrib>Linn, S C</creatorcontrib><creatorcontrib>Sonke, G S</creatorcontrib><creatorcontrib>van Werkhoven, E</creatorcontrib><creatorcontrib>Lips, E H</creatorcontrib><creatorcontrib>Warnars, H A</creatorcontrib><creatorcontrib>Doll, P K</creatorcontrib><creatorcontrib>Bruining, A</creatorcontrib><creatorcontrib>Mandjes, I A</creatorcontrib><creatorcontrib>Vrancken Peeters, M J</creatorcontrib><creatorcontrib>Wesseling, J</creatorcontrib><creatorcontrib>Gilhuijs, K G</creatorcontrib><creatorcontrib>Rodenhuis, S</creatorcontrib><title>Neoadjuvant chemotherapy adaptation and serial MRI response monitoring in ER-positive HER2-negative breast cancer</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Background:
Changing the neoadjuvant chemotherapy regimen in insufficiently responding breast cancer is not a standard policy. We analysed a series of patients with ‘luminal’-type breast cancer in whom the second half of neoadjuvant chemotherapy was selected based on the response to the first half.
Methods:
Patients with oestrogen receptor-positive (ER+) human epidermal growth factor receptor 2-negative (HER2−) breast cancer received three courses of neoadjuvant dose-dense doxorubicin and cyclophosphamide (ddAC). Three further courses of ddAC were administered in case of a ‘favourable response’ on the interim magnetic resonance imaging (MRI) and a switch to docetaxel and capecitabine (DC) was made in case of an ‘unfavourable response’, using previously published response criteria. The efficacy of this approach was evaluated by tumour size reductions on serial contrast-enhanced MRI, pathologic response and relapse-free survival.
Results:
Two hundred and forty-six patients received three courses of ddAC. One hundred and sixty-four patients (67%) had a favourable response at the interim MRI, with a mean tumour size reduction of 31% after the first three courses and 34% after the second three courses. Patients with unfavourable responsive tumours had a mean tumour size reduction of 12% after three courses and received three courses of DC rather than ddAC. This led to a mean shrinkage of 27%.
Conclusion:
The tumour size reduction of initially less responsive tumours after treatment adaptation adds further evidence that a response-adapted strategy may enhance the efficacy of neoadjuvant chemotherapy.</description><subject>692/699/67/1059/99</subject><subject>692/699/67/1347</subject><subject>692/700/1421/1628</subject><subject>Adaptation</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer Research</subject><subject>Cancer therapies</subject><subject>Capecitabine</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Clinical Study</subject><subject>Clinical trials</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Deoxycytidine - administration & dosage</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Doxorubicin - administration & dosage</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Epidermal growth factor</subject><subject>Female</subject><subject>Filgrastim</subject><subject>Fluorouracil - administration & dosage</subject><subject>Fluorouracil - analogs & derivatives</subject><subject>Granulocyte Colony-Stimulating Factor - administration & dosage</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Magnetic Resonance Imaging</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Neoadjuvant Therapy</subject><subject>Oncology</subject><subject>Receptor, ErbB-2 - biosynthesis</subject><subject>Receptors, Estrogen - biosynthesis</subject><subject>Recombinant Proteins - administration & dosage</subject><subject>Survival Analysis</subject><subject>Taxoids - administration & dosage</subject><subject>Tumors</subject><subject>Young Adult</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkU2LUzEUhoMoTh3duZaAuPPWJPcj924EGaozMCoUXYeT5Nw2pU3uJGlh_r2preMIrsIhD-97OA8hrzmbc1b3H_TGzAXj9bzr-BMy420tKt4L-ZTMGGOyYoNgF-RFSpsyDqyXz8mFaHgzcNnPyN03DGA3-wP4TM0adyGvMcJ0T8HClCG74Cl4SxNGB1v6dXlDI6Yp-IR0F7zLITq_os7TxbKaQnLZHZBeL5ai8riC35OOCKnEgzcYX5JnI2wTvjq_l-Tn58WPq-vq9vuXm6tPt5VpeparAVthtZZgoNMG2MC5HWsxMoncMuw5A40dWDM2XSdboWXfmsFKywXTfND1Jfl4yp32eofWoM8RtmqKbgfxXgVw6t8f79ZqFQ6q7tthaJoS8PYcEMPdHlNWm7CPvuyseOlsWy4ZK9T7E2ViSCni-NDAmToKUkWQOgpSRVDB3zze6gH-Y6QA784AJAPbMZajufSX61nTdp0oXHXi0nQUgPHRdv8r_gVtZ6qD</recordid><startdate>20131210</startdate><enddate>20131210</enddate><creator>Rigter, L S</creator><creator>Loo, C E</creator><creator>Linn, S C</creator><creator>Sonke, G S</creator><creator>van Werkhoven, E</creator><creator>Lips, E H</creator><creator>Warnars, H A</creator><creator>Doll, P K</creator><creator>Bruining, A</creator><creator>Mandjes, I A</creator><creator>Vrancken Peeters, M J</creator><creator>Wesseling, J</creator><creator>Gilhuijs, K G</creator><creator>Rodenhuis, S</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>IQODW</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>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20131210</creationdate><title>Neoadjuvant chemotherapy adaptation and serial MRI response monitoring in ER-positive HER2-negative breast cancer</title><author>Rigter, L S ; Loo, C E ; Linn, S C ; Sonke, G S ; van Werkhoven, E ; Lips, E H ; Warnars, H A ; Doll, P K ; Bruining, A ; Mandjes, I A ; Vrancken Peeters, M J ; Wesseling, J ; Gilhuijs, K G ; Rodenhuis, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-9e52dbb7aca6bca0911df32f07e1d0e810abe6adcf466752b785c9d7d120b19b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>692/699/67/1059/99</topic><topic>692/699/67/1347</topic><topic>692/700/1421/1628</topic><topic>Adaptation</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer Research</topic><topic>Cancer therapies</topic><topic>Capecitabine</topic><topic>Chemotherapy</topic><topic>Chemotherapy, Adjuvant</topic><topic>Clinical Study</topic><topic>Clinical trials</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Deoxycytidine - administration & dosage</topic><topic>Deoxycytidine - analogs & derivatives</topic><topic>Doxorubicin - administration & dosage</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Epidermal growth factor</topic><topic>Female</topic><topic>Filgrastim</topic><topic>Fluorouracil - administration & dosage</topic><topic>Fluorouracil - analogs & derivatives</topic><topic>Granulocyte Colony-Stimulating Factor - administration & dosage</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Magnetic Resonance Imaging</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Medicine</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Neoadjuvant Therapy</topic><topic>Oncology</topic><topic>Receptor, ErbB-2 - biosynthesis</topic><topic>Receptors, Estrogen - biosynthesis</topic><topic>Recombinant Proteins - administration & dosage</topic><topic>Survival Analysis</topic><topic>Taxoids - administration & dosage</topic><topic>Tumors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rigter, L S</creatorcontrib><creatorcontrib>Loo, C E</creatorcontrib><creatorcontrib>Linn, S C</creatorcontrib><creatorcontrib>Sonke, G S</creatorcontrib><creatorcontrib>van Werkhoven, E</creatorcontrib><creatorcontrib>Lips, E H</creatorcontrib><creatorcontrib>Warnars, H A</creatorcontrib><creatorcontrib>Doll, P K</creatorcontrib><creatorcontrib>Bruining, A</creatorcontrib><creatorcontrib>Mandjes, I A</creatorcontrib><creatorcontrib>Vrancken Peeters, M J</creatorcontrib><creatorcontrib>Wesseling, J</creatorcontrib><creatorcontrib>Gilhuijs, K G</creatorcontrib><creatorcontrib>Rodenhuis, S</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Pascal-Francis</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>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS 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>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</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>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rigter, L S</au><au>Loo, C E</au><au>Linn, S C</au><au>Sonke, G S</au><au>van Werkhoven, E</au><au>Lips, E H</au><au>Warnars, H A</au><au>Doll, P K</au><au>Bruining, A</au><au>Mandjes, I A</au><au>Vrancken Peeters, M J</au><au>Wesseling, J</au><au>Gilhuijs, K G</au><au>Rodenhuis, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neoadjuvant chemotherapy adaptation and serial MRI response monitoring in ER-positive HER2-negative breast cancer</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>2013-12-10</date><risdate>2013</risdate><volume>109</volume><issue>12</issue><spage>2965</spage><epage>2972</epage><pages>2965-2972</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Background:
Changing the neoadjuvant chemotherapy regimen in insufficiently responding breast cancer is not a standard policy. We analysed a series of patients with ‘luminal’-type breast cancer in whom the second half of neoadjuvant chemotherapy was selected based on the response to the first half.
Methods:
Patients with oestrogen receptor-positive (ER+) human epidermal growth factor receptor 2-negative (HER2−) breast cancer received three courses of neoadjuvant dose-dense doxorubicin and cyclophosphamide (ddAC). Three further courses of ddAC were administered in case of a ‘favourable response’ on the interim magnetic resonance imaging (MRI) and a switch to docetaxel and capecitabine (DC) was made in case of an ‘unfavourable response’, using previously published response criteria. The efficacy of this approach was evaluated by tumour size reductions on serial contrast-enhanced MRI, pathologic response and relapse-free survival.
Results:
Two hundred and forty-six patients received three courses of ddAC. One hundred and sixty-four patients (67%) had a favourable response at the interim MRI, with a mean tumour size reduction of 31% after the first three courses and 34% after the second three courses. Patients with unfavourable responsive tumours had a mean tumour size reduction of 12% after three courses and received three courses of DC rather than ddAC. This led to a mean shrinkage of 27%.
Conclusion:
The tumour size reduction of initially less responsive tumours after treatment adaptation adds further evidence that a response-adapted strategy may enhance the efficacy of neoadjuvant chemotherapy.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24149178</pmid><doi>10.1038/bjc.2013.661</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 692/699/67/1059/99 692/699/67/1347 692/700/1421/1628 Adaptation Adolescent Adult Aged Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Biomedical and Life Sciences Biomedicine Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Breast Neoplasms - pathology Cancer Research Cancer therapies Capecitabine Chemotherapy Chemotherapy, Adjuvant Clinical Study Clinical trials Cyclophosphamide - administration & dosage Deoxycytidine - administration & dosage Deoxycytidine - analogs & derivatives Doxorubicin - administration & dosage Drug Resistance Epidemiology Epidermal growth factor Female Filgrastim Fluorouracil - administration & dosage Fluorouracil - analogs & derivatives Granulocyte Colony-Stimulating Factor - administration & dosage Gynecology. Andrology. Obstetrics Humans Immunohistochemistry Magnetic Resonance Imaging Mammary gland diseases Medical sciences Middle Aged Molecular Medicine Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Neoadjuvant Therapy Oncology Receptor, ErbB-2 - biosynthesis Receptors, Estrogen - biosynthesis Recombinant Proteins - administration & dosage Survival Analysis Taxoids - administration & dosage Tumors Young Adult |
title | Neoadjuvant chemotherapy adaptation and serial MRI response monitoring in ER-positive HER2-negative breast cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T14%3A12%3A01IST&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=Neoadjuvant%20chemotherapy%20adaptation%20and%20serial%20MRI%20response%20monitoring%20in%20ER-positive%20HER2-negative%20breast%20cancer&rft.jtitle=British%20journal%20of%20cancer&rft.au=Rigter,%20L%20S&rft.date=2013-12-10&rft.volume=109&rft.issue=12&rft.spage=2965&rft.epage=2972&rft.pages=2965-2972&rft.issn=0007-0920&rft.eissn=1532-1827&rft.coden=BJCAAI&rft_id=info:doi/10.1038/bjc.2013.661&rft_dat=%3Cproquest_pubme%3E3152271441%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=1466551700&rft_id=info:pmid/24149178&rfr_iscdi=true |