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
Hauptverfasser: 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
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container_end_page 2972
container_issue 12
container_start_page 2965
container_title British journal of cancer
container_volume 109
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
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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%. 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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&amp;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. 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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. 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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
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