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Radiologic complete response (rCR) in contrast-enhanced magnetic resonance imaging (CE-MRI) after neoadjuvant chemotherapy for early breast cancer predicts recurrence-free survival but not pathologic complete response (pCR)
Patients with early breast cancer (EBC) achieving pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) have a favorable prognosis. Breast surgery might be avoided in patients in whom the presence of residual tumor can be ruled out with high confidence. Here, we investigated the d...
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Published in: | Breast cancer research : BCR 2019-01, Vol.21 (1), p.19-19, Article 19 |
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creator | Gampenrieder, Simon Peter Peer, Andreas Weismann, Christian Meissnitzer, Matthias Rinnerthaler, Gabriel Webhofer, Johanna Westphal, Theresa Riedmann, Marina Meissnitzer, Thomas Egger, Heike Klaassen Federspiel, Frederike Reitsamer, Roland Hauser-Kronberger, Cornelia Stering, Katharina Hergan, Klaus Mlineritsch, Brigitte Greil, Richard |
description | Patients with early breast cancer (EBC) achieving pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) have a favorable prognosis. Breast surgery might be avoided in patients in whom the presence of residual tumor can be ruled out with high confidence. Here, we investigated the diagnostic accuracy of contrast-enhanced MRI (CE-MRI) in predicting pCR and long-term outcome after NACT.
Patients with EBC, including patients with locally advanced disease, who had undergone CE-MRI after NACT, were retrospectively analyzed (n = 246). Three radiologists, blinded to clinicopathologic data, reevaluated all MRI scans regarding to the absence (radiologic complete remission; rCR) or presence (no-rCR) of residual contrast enhancement. Clinical and pathologic responses were compared categorically using Cohen's kappa statistic. The Kaplan-Meier method was used to estimate recurrence-free survival (RFS) and overall survival (OS).
Overall rCR and pCR (no invasive tumor in the breast and axilla (ypT0/is N0)) rates were 45% (111/246) and 29% (71/246), respectively. Only 48% (53/111; 95% CI 38-57%) of rCR corresponded to a pCR (= positive predictive value - PPV). Conversely, in 87% (117/135; 95% CI 79-92%) of patients, residual tumor observed on MRI was pathologically confirmed (= negative predictive value - NPV). Sensitivity to detect a pCR was 75% (53/71; 95% CI 63-84%), while specificity to detect residual tumor and accuracy were 67% (117/175; 95% CI 59-74%) and 69% (170/246; 95% CI 63-75%), respectively. The PPV was significantly lower in hormone-receptor (HR)-positive compared to HR-negative tumors (17/52 = 33% vs. 36/59 = 61%; P = 0.004). The concordance between rCR and pCR was low (Cohen's kappa - 0.1), however in multivariate analysis both assessments were significantly associated with RFS (rCR P = 0.037; pCR P = 0.033) and OS (rCR P = 0.033; pCR P = 0.043).
Preoperative CE-MRI did not accurately predict pCR after NACT for EBC, especially not in HR-positive tumors. However, rCR was strongly associated with favorable RFS and OS. |
doi_str_mv | 10.1186/s13058-018-1091-y |
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Patients with EBC, including patients with locally advanced disease, who had undergone CE-MRI after NACT, were retrospectively analyzed (n = 246). Three radiologists, blinded to clinicopathologic data, reevaluated all MRI scans regarding to the absence (radiologic complete remission; rCR) or presence (no-rCR) of residual contrast enhancement. Clinical and pathologic responses were compared categorically using Cohen's kappa statistic. The Kaplan-Meier method was used to estimate recurrence-free survival (RFS) and overall survival (OS).
Overall rCR and pCR (no invasive tumor in the breast and axilla (ypT0/is N0)) rates were 45% (111/246) and 29% (71/246), respectively. Only 48% (53/111; 95% CI 38-57%) of rCR corresponded to a pCR (= positive predictive value - PPV). Conversely, in 87% (117/135; 95% CI 79-92%) of patients, residual tumor observed on MRI was pathologically confirmed (= negative predictive value - NPV). Sensitivity to detect a pCR was 75% (53/71; 95% CI 63-84%), while specificity to detect residual tumor and accuracy were 67% (117/175; 95% CI 59-74%) and 69% (170/246; 95% CI 63-75%), respectively. The PPV was significantly lower in hormone-receptor (HR)-positive compared to HR-negative tumors (17/52 = 33% vs. 36/59 = 61%; P = 0.004). The concordance between rCR and pCR was low (Cohen's kappa - 0.1), however in multivariate analysis both assessments were significantly associated with RFS (rCR P = 0.037; pCR P = 0.033) and OS (rCR P = 0.033; pCR P = 0.043).
Preoperative CE-MRI did not accurately predict pCR after NACT for EBC, especially not in HR-positive tumors. However, rCR was strongly associated with favorable RFS and OS.</description><identifier>ISSN: 1465-542X</identifier><identifier>ISSN: 1465-5411</identifier><identifier>EISSN: 1465-542X</identifier><identifier>DOI: 10.1186/s13058-018-1091-y</identifier><identifier>PMID: 30704493</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Accuracy ; Adult ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biopsy ; Breast - diagnostic imaging ; Breast - pathology ; Breast - surgery ; Breast cancer ; Breast Neoplasms - diagnostic imaging ; Breast Neoplasms - mortality ; Breast Neoplasms - pathology ; Breast Neoplasms - therapy ; Cancer therapies ; Chemotherapy ; Contrast Media - administration & dosage ; Disease-Free Survival ; Female ; Follow-Up Studies ; Humans ; Invasiveness ; Kaplan-Meier Estimate ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Mammography ; Mastectomy ; Medical imaging ; Medical prognosis ; Middle Aged ; MRI ; Multivariate analysis ; Neoadjuvant chemotherapy ; Neoadjuvant Therapy - methods ; Neoplasm Recurrence, Local - diagnosis ; Neoplasm, Residual ; NMR ; Nuclear magnetic resonance ; Prediction of complete pathologic response ; Predictive Value of Tests ; Preoperative Period ; Prognosis ; Remission ; Retrospective Studies ; Surgery ; Survival ; Tumors ; Young Adult</subject><ispartof>Breast cancer research : BCR, 2019-01, Vol.21 (1), p.19-19, Article 19</ispartof><rights>Copyright © 2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s). 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-87935bbe788615b6162c484d9a59529a40c2a36fe92f28b769aea2a946ec430e3</citedby><cites>FETCH-LOGICAL-c493t-87935bbe788615b6162c484d9a59529a40c2a36fe92f28b769aea2a946ec430e3</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/PMC6357474/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2183417385?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30704493$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gampenrieder, Simon Peter</creatorcontrib><creatorcontrib>Peer, Andreas</creatorcontrib><creatorcontrib>Weismann, Christian</creatorcontrib><creatorcontrib>Meissnitzer, Matthias</creatorcontrib><creatorcontrib>Rinnerthaler, Gabriel</creatorcontrib><creatorcontrib>Webhofer, Johanna</creatorcontrib><creatorcontrib>Westphal, Theresa</creatorcontrib><creatorcontrib>Riedmann, Marina</creatorcontrib><creatorcontrib>Meissnitzer, Thomas</creatorcontrib><creatorcontrib>Egger, Heike</creatorcontrib><creatorcontrib>Klaassen Federspiel, Frederike</creatorcontrib><creatorcontrib>Reitsamer, Roland</creatorcontrib><creatorcontrib>Hauser-Kronberger, Cornelia</creatorcontrib><creatorcontrib>Stering, Katharina</creatorcontrib><creatorcontrib>Hergan, Klaus</creatorcontrib><creatorcontrib>Mlineritsch, Brigitte</creatorcontrib><creatorcontrib>Greil, Richard</creatorcontrib><title>Radiologic complete response (rCR) in contrast-enhanced magnetic resonance imaging (CE-MRI) after neoadjuvant chemotherapy for early breast cancer predicts recurrence-free survival but not pathologic complete response (pCR)</title><title>Breast cancer research : BCR</title><addtitle>Breast Cancer Res</addtitle><description>Patients with early breast cancer (EBC) achieving pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) have a favorable prognosis. Breast surgery might be avoided in patients in whom the presence of residual tumor can be ruled out with high confidence. Here, we investigated the diagnostic accuracy of contrast-enhanced MRI (CE-MRI) in predicting pCR and long-term outcome after NACT.
Patients with EBC, including patients with locally advanced disease, who had undergone CE-MRI after NACT, were retrospectively analyzed (n = 246). Three radiologists, blinded to clinicopathologic data, reevaluated all MRI scans regarding to the absence (radiologic complete remission; rCR) or presence (no-rCR) of residual contrast enhancement. Clinical and pathologic responses were compared categorically using Cohen's kappa statistic. The Kaplan-Meier method was used to estimate recurrence-free survival (RFS) and overall survival (OS).
Overall rCR and pCR (no invasive tumor in the breast and axilla (ypT0/is N0)) rates were 45% (111/246) and 29% (71/246), respectively. Only 48% (53/111; 95% CI 38-57%) of rCR corresponded to a pCR (= positive predictive value - PPV). Conversely, in 87% (117/135; 95% CI 79-92%) of patients, residual tumor observed on MRI was pathologically confirmed (= negative predictive value - NPV). Sensitivity to detect a pCR was 75% (53/71; 95% CI 63-84%), while specificity to detect residual tumor and accuracy were 67% (117/175; 95% CI 59-74%) and 69% (170/246; 95% CI 63-75%), respectively. The PPV was significantly lower in hormone-receptor (HR)-positive compared to HR-negative tumors (17/52 = 33% vs. 36/59 = 61%; P = 0.004). The concordance between rCR and pCR was low (Cohen's kappa - 0.1), however in multivariate analysis both assessments were significantly associated with RFS (rCR P = 0.037; pCR P = 0.033) and OS (rCR P = 0.033; pCR P = 0.043).
Preoperative CE-MRI did not accurately predict pCR after NACT for EBC, especially not in HR-positive tumors. However, rCR was strongly associated with favorable RFS and OS.</description><subject>Accuracy</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biopsy</subject><subject>Breast - diagnostic imaging</subject><subject>Breast - pathology</subject><subject>Breast - surgery</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - diagnostic imaging</subject><subject>Breast Neoplasms - mortality</subject><subject>Breast Neoplasms - pathology</subject><subject>Breast Neoplasms - therapy</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Contrast Media - administration & dosage</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Invasiveness</subject><subject>Kaplan-Meier Estimate</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Mammography</subject><subject>Mastectomy</subject><subject>Medical imaging</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>MRI</subject><subject>Multivariate analysis</subject><subject>Neoadjuvant chemotherapy</subject><subject>Neoadjuvant Therapy - methods</subject><subject>Neoplasm Recurrence, Local - diagnosis</subject><subject>Neoplasm, Residual</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Prediction of complete pathologic response</subject><subject>Predictive Value of Tests</subject><subject>Preoperative Period</subject><subject>Prognosis</subject><subject>Remission</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Survival</subject><subject>Tumors</subject><subject>Young Adult</subject><issn>1465-542X</issn><issn>1465-5411</issn><issn>1465-542X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1ktGK1DAUhoso7rr6AN5IwJvZi65Jk7TpjbAMqw6sCIOCd-E0PZ3p0Elqkg7M0_oqps7usit4lXDOfz5O_vxZ9pbRK8ZU-SEwTqXKKVM5ozXLj8-ycyZKmUtR_Hz-6H6WvQphRymrlFQvszNOKypEzc-z32toeze4TW-IcftxwIjEYxidDUgWfrm-JL1NLRs9hJij3YI12JI9bCzGNJXEzs410qdabzdksbzJv65XlwS6iJ5YdNDupgPYSMwW9y5u0cN4JJ3zBMEPR9J4THBiZowno8e2NzEktJm8x1TMO49IwuQP_QEG0kyRWBfJCHH7_-XHtPzr7EUHQ8A3d-dF9uPTzffll_z22-fV8vo2N8mGmKuq5rJpsFKqZLIpWVkYoURbg6xlUYOgpgBedlgXXaGaqqwBoYBalGgEp8gvstWJ2zrY6dEnL_xRO-j134LzGw0-2TWgljDPMc7LFgSqTnHaMmpawwvGpWoS6-OJNU7NHluDs_fDE-jTju23euMOuuSyEpVIgMUdwLtfE4ao930wOAyQ_mIKumBVLSSrJE_S9_9Id27yNlmVVIoLVnElk4qdVMa7EDx2D8swquco6lMUdYqinqOoj2nm3eNXPEzcZ4__AZcm3zc</recordid><startdate>20190131</startdate><enddate>20190131</enddate><creator>Gampenrieder, Simon Peter</creator><creator>Peer, Andreas</creator><creator>Weismann, Christian</creator><creator>Meissnitzer, Matthias</creator><creator>Rinnerthaler, Gabriel</creator><creator>Webhofer, Johanna</creator><creator>Westphal, Theresa</creator><creator>Riedmann, Marina</creator><creator>Meissnitzer, Thomas</creator><creator>Egger, Heike</creator><creator>Klaassen Federspiel, Frederike</creator><creator>Reitsamer, Roland</creator><creator>Hauser-Kronberger, Cornelia</creator><creator>Stering, Katharina</creator><creator>Hergan, Klaus</creator><creator>Mlineritsch, Brigitte</creator><creator>Greil, Richard</creator><general>BioMed Central</general><general>BMC</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>8FI</scope><scope>8FJ</scope><scope>8FK</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20190131</creationdate><title>Radiologic complete response (rCR) in contrast-enhanced magnetic resonance imaging (CE-MRI) after neoadjuvant chemotherapy for early breast cancer predicts recurrence-free survival but not pathologic complete response (pCR)</title><author>Gampenrieder, Simon Peter ; Peer, Andreas ; Weismann, Christian ; Meissnitzer, Matthias ; Rinnerthaler, Gabriel ; Webhofer, Johanna ; Westphal, Theresa ; Riedmann, Marina ; Meissnitzer, Thomas ; Egger, Heike ; Klaassen Federspiel, Frederike ; Reitsamer, Roland ; Hauser-Kronberger, Cornelia ; Stering, Katharina ; Hergan, Klaus ; Mlineritsch, Brigitte ; Greil, Richard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-87935bbe788615b6162c484d9a59529a40c2a36fe92f28b769aea2a946ec430e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Accuracy</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biopsy</topic><topic>Breast - diagnostic imaging</topic><topic>Breast - pathology</topic><topic>Breast - surgery</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - diagnostic imaging</topic><topic>Breast Neoplasms - mortality</topic><topic>Breast Neoplasms - pathology</topic><topic>Breast Neoplasms - therapy</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Contrast Media - administration & dosage</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Invasiveness</topic><topic>Kaplan-Meier Estimate</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Mammography</topic><topic>Mastectomy</topic><topic>Medical imaging</topic><topic>Medical prognosis</topic><topic>Middle Aged</topic><topic>MRI</topic><topic>Multivariate analysis</topic><topic>Neoadjuvant chemotherapy</topic><topic>Neoadjuvant Therapy - methods</topic><topic>Neoplasm Recurrence, Local - diagnosis</topic><topic>Neoplasm, Residual</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Prediction of complete pathologic response</topic><topic>Predictive Value of Tests</topic><topic>Preoperative Period</topic><topic>Prognosis</topic><topic>Remission</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Survival</topic><topic>Tumors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gampenrieder, Simon Peter</creatorcontrib><creatorcontrib>Peer, Andreas</creatorcontrib><creatorcontrib>Weismann, Christian</creatorcontrib><creatorcontrib>Meissnitzer, Matthias</creatorcontrib><creatorcontrib>Rinnerthaler, Gabriel</creatorcontrib><creatorcontrib>Webhofer, Johanna</creatorcontrib><creatorcontrib>Westphal, Theresa</creatorcontrib><creatorcontrib>Riedmann, Marina</creatorcontrib><creatorcontrib>Meissnitzer, Thomas</creatorcontrib><creatorcontrib>Egger, Heike</creatorcontrib><creatorcontrib>Klaassen Federspiel, Frederike</creatorcontrib><creatorcontrib>Reitsamer, Roland</creatorcontrib><creatorcontrib>Hauser-Kronberger, Cornelia</creatorcontrib><creatorcontrib>Stering, Katharina</creatorcontrib><creatorcontrib>Hergan, Klaus</creatorcontrib><creatorcontrib>Mlineritsch, Brigitte</creatorcontrib><creatorcontrib>Greil, Richard</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>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Breast cancer research : BCR</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gampenrieder, Simon Peter</au><au>Peer, Andreas</au><au>Weismann, Christian</au><au>Meissnitzer, Matthias</au><au>Rinnerthaler, Gabriel</au><au>Webhofer, Johanna</au><au>Westphal, Theresa</au><au>Riedmann, Marina</au><au>Meissnitzer, Thomas</au><au>Egger, Heike</au><au>Klaassen Federspiel, Frederike</au><au>Reitsamer, Roland</au><au>Hauser-Kronberger, Cornelia</au><au>Stering, Katharina</au><au>Hergan, Klaus</au><au>Mlineritsch, Brigitte</au><au>Greil, Richard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiologic complete response (rCR) in contrast-enhanced magnetic resonance imaging (CE-MRI) after neoadjuvant chemotherapy for early breast cancer predicts recurrence-free survival but not pathologic complete response (pCR)</atitle><jtitle>Breast cancer research : BCR</jtitle><addtitle>Breast Cancer Res</addtitle><date>2019-01-31</date><risdate>2019</risdate><volume>21</volume><issue>1</issue><spage>19</spage><epage>19</epage><pages>19-19</pages><artnum>19</artnum><issn>1465-542X</issn><issn>1465-5411</issn><eissn>1465-542X</eissn><abstract>Patients with early breast cancer (EBC) achieving pathologic complete response (pCR) after neoadjuvant chemotherapy (NACT) have a favorable prognosis. Breast surgery might be avoided in patients in whom the presence of residual tumor can be ruled out with high confidence. Here, we investigated the diagnostic accuracy of contrast-enhanced MRI (CE-MRI) in predicting pCR and long-term outcome after NACT.
Patients with EBC, including patients with locally advanced disease, who had undergone CE-MRI after NACT, were retrospectively analyzed (n = 246). Three radiologists, blinded to clinicopathologic data, reevaluated all MRI scans regarding to the absence (radiologic complete remission; rCR) or presence (no-rCR) of residual contrast enhancement. Clinical and pathologic responses were compared categorically using Cohen's kappa statistic. The Kaplan-Meier method was used to estimate recurrence-free survival (RFS) and overall survival (OS).
Overall rCR and pCR (no invasive tumor in the breast and axilla (ypT0/is N0)) rates were 45% (111/246) and 29% (71/246), respectively. Only 48% (53/111; 95% CI 38-57%) of rCR corresponded to a pCR (= positive predictive value - PPV). Conversely, in 87% (117/135; 95% CI 79-92%) of patients, residual tumor observed on MRI was pathologically confirmed (= negative predictive value - NPV). Sensitivity to detect a pCR was 75% (53/71; 95% CI 63-84%), while specificity to detect residual tumor and accuracy were 67% (117/175; 95% CI 59-74%) and 69% (170/246; 95% CI 63-75%), respectively. The PPV was significantly lower in hormone-receptor (HR)-positive compared to HR-negative tumors (17/52 = 33% vs. 36/59 = 61%; P = 0.004). The concordance between rCR and pCR was low (Cohen's kappa - 0.1), however in multivariate analysis both assessments were significantly associated with RFS (rCR P = 0.037; pCR P = 0.033) and OS (rCR P = 0.033; pCR P = 0.043).
Preoperative CE-MRI did not accurately predict pCR after NACT for EBC, especially not in HR-positive tumors. However, rCR was strongly associated with favorable RFS and OS.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>30704493</pmid><doi>10.1186/s13058-018-1091-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1465-542X |
ispartof | Breast cancer research : BCR, 2019-01, Vol.21 (1), p.19-19, Article 19 |
issn | 1465-542X 1465-5411 1465-542X |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_5aa9461336da4e8f830d10cdc321358b |
source | Open Access: PubMed Central; Publicly Available Content (ProQuest) |
subjects | Accuracy Adult Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biopsy Breast - diagnostic imaging Breast - pathology Breast - surgery Breast cancer Breast Neoplasms - diagnostic imaging Breast Neoplasms - mortality Breast Neoplasms - pathology Breast Neoplasms - therapy Cancer therapies Chemotherapy Contrast Media - administration & dosage Disease-Free Survival Female Follow-Up Studies Humans Invasiveness Kaplan-Meier Estimate Magnetic resonance imaging Magnetic Resonance Imaging - methods Mammography Mastectomy Medical imaging Medical prognosis Middle Aged MRI Multivariate analysis Neoadjuvant chemotherapy Neoadjuvant Therapy - methods Neoplasm Recurrence, Local - diagnosis Neoplasm, Residual NMR Nuclear magnetic resonance Prediction of complete pathologic response Predictive Value of Tests Preoperative Period Prognosis Remission Retrospective Studies Surgery Survival Tumors Young Adult |
title | Radiologic complete response (rCR) in contrast-enhanced magnetic resonance imaging (CE-MRI) after neoadjuvant chemotherapy for early breast cancer predicts recurrence-free survival but not pathologic complete response (pCR) |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T04%3A12%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Radiologic%20complete%20response%20(rCR)%20in%20contrast-enhanced%20magnetic%20resonance%20imaging%20(CE-MRI)%20after%20neoadjuvant%20chemotherapy%20for%20early%20breast%20cancer%20predicts%20recurrence-free%20survival%20but%20not%20pathologic%20complete%20response%20(pCR)&rft.jtitle=Breast%20cancer%20research%20:%20BCR&rft.au=Gampenrieder,%20Simon%20Peter&rft.date=2019-01-31&rft.volume=21&rft.issue=1&rft.spage=19&rft.epage=19&rft.pages=19-19&rft.artnum=19&rft.issn=1465-542X&rft.eissn=1465-542X&rft_id=info:doi/10.1186/s13058-018-1091-y&rft_dat=%3Cproquest_doaj_%3E2183417385%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c493t-87935bbe788615b6162c484d9a59529a40c2a36fe92f28b769aea2a946ec430e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2183417385&rft_id=info:pmid/30704493&rfr_iscdi=true |