Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients

We evaluated the prognostic implications of the circulating tumor cell (CTC) count in non-metastatic, HER2-negative breast cancer patients who failed to achieve pathologic complete response (pCR) after neoadjuvant chemotherapy (NCT). A total of 173, non-metastatic breast cancer patients treated with...

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Veröffentlicht in:Scientific reports 2020-10, Vol.10 (1), p.17466-17466, Article 17466
Hauptverfasser: Gwark, Sungchan, Kim, Jisun, Kwon, Nak-Jung, Kim, Kyoung-Yeon, Kim, YongNam, Lee, Cham Han, Kim, Young Hun, Kim, Myoung Shin, Hong, Sung Woo, Choi, Mi Young, Jeon, Byung Hee, Chang, Suhwan, Yu, Jonghan, Park, Ji Yeon, Lee, Hee Jin, Lee, Sae Byul, Chung, Il Yong, Ko, Beom Seok, Kim, Hee Jeong, Lee, Jong Won, Son, Byung Ho, Ahn, Jin-Hee, Jung, Kyung Hae, Kim, Sung-Bae, Gong, Gyung-Yub, Ahn, Sei Hyun
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container_title Scientific reports
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creator Gwark, Sungchan
Kim, Jisun
Kwon, Nak-Jung
Kim, Kyoung-Yeon
Kim, YongNam
Lee, Cham Han
Kim, Young Hun
Kim, Myoung Shin
Hong, Sung Woo
Choi, Mi Young
Jeon, Byung Hee
Chang, Suhwan
Yu, Jonghan
Park, Ji Yeon
Lee, Hee Jin
Lee, Sae Byul
Chung, Il Yong
Ko, Beom Seok
Kim, Hee Jeong
Lee, Jong Won
Son, Byung Ho
Ahn, Jin-Hee
Jung, Kyung Hae
Kim, Sung-Bae
Gong, Gyung-Yub
Ahn, Sei Hyun
description We evaluated the prognostic implications of the circulating tumor cell (CTC) count in non-metastatic, HER2-negative breast cancer patients who failed to achieve pathologic complete response (pCR) after neoadjuvant chemotherapy (NCT). A total of 173, non-metastatic breast cancer patients treated with NCT were prospectively enrolled. CTCs were obtained from blood drawn pre-NCT and post-NCT using a SMART BIOPSY SYSTEM isolation kit (Cytogen Inc., Seoul, Korea) with immunofluorescence staining. Excluding 26 HER2-positive patients, Relapse-free survival (RFS) and overall survival (OS) related to the CTC count and the association of the CTC count with the treatment response to given therapy were analyzed in 147 HER2-negative patients. Among 147 HER2-negative patients, 28 relapses (19.0%) and 13 deaths (8.8%, all breast cancer-specific) were observed during a median follow-up of 37.3 months. One hundred and seven patients (72.8%) were hormone receptor-positive, and 40 patients (27.2%) had triple-negative breast cancer (TNBC). One or more CTCs were identified in 88 of the 147 patients (59.9%) before NCT and 77 of the 134 patients (52.4%) after NCT. In the entire HER2-negative patient cohort, the initial nodal status was the most significant factor influencing RFS and OS. In TNBC, 11 patients (27.5%) achieved pCR and patients that failed to achieve pCR with ≥ 5 CTCs after NCT, showed worse RFS (HR, 10.66; 95% CI, 1.80–63.07; p  = 0.009) and OS (HR, 14.00; 95% CI, 1.26–155.53; p  = 0.032). The patients with residual tumor and a high number of the CTCs after NCT displayed the worse outcome. These findings could provide justification to launch a future, well designed trial with longer follow-up data to obtain regulatory approval for clinical use of the assay, especially for the ER-positive, HER2-negative breast cancer subset.
doi_str_mv 10.1038/s41598-020-74577-w
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A total of 173, non-metastatic breast cancer patients treated with NCT were prospectively enrolled. CTCs were obtained from blood drawn pre-NCT and post-NCT using a SMART BIOPSY SYSTEM isolation kit (Cytogen Inc., Seoul, Korea) with immunofluorescence staining. Excluding 26 HER2-positive patients, Relapse-free survival (RFS) and overall survival (OS) related to the CTC count and the association of the CTC count with the treatment response to given therapy were analyzed in 147 HER2-negative patients. Among 147 HER2-negative patients, 28 relapses (19.0%) and 13 deaths (8.8%, all breast cancer-specific) were observed during a median follow-up of 37.3 months. One hundred and seven patients (72.8%) were hormone receptor-positive, and 40 patients (27.2%) had triple-negative breast cancer (TNBC). One or more CTCs were identified in 88 of the 147 patients (59.9%) before NCT and 77 of the 134 patients (52.4%) after NCT. In the entire HER2-negative patient cohort, the initial nodal status was the most significant factor influencing RFS and OS. In TNBC, 11 patients (27.5%) achieved pCR and patients that failed to achieve pCR with ≥ 5 CTCs after NCT, showed worse RFS (HR, 10.66; 95% CI, 1.80–63.07; p  = 0.009) and OS (HR, 14.00; 95% CI, 1.26–155.53; p  = 0.032). The patients with residual tumor and a high number of the CTCs after NCT displayed the worse outcome. These findings could provide justification to launch a future, well designed trial with longer follow-up data to obtain regulatory approval for clinical use of the assay, especially for the ER-positive, HER2-negative breast cancer subset.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-74577-w</identifier><identifier>PMID: 33060768</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67/1347 ; 631/67/1857 ; 692/4028/67/1347 ; Adult ; Aged ; Biomarkers, Tumor - metabolism ; Biopsy ; Breast cancer ; Breast Neoplasms - blood ; Breast Neoplasms - drug therapy ; Cancer therapies ; Cell Count ; Chemotherapy ; Chemotherapy, Adjuvant ; Disease-Free Survival ; ErbB-2 protein ; Estrogen Receptor alpha - metabolism ; Female ; Follow-Up Studies ; Humanities and Social Sciences ; Humans ; Immunofluorescence ; MCF-7 Cells ; Metastases ; Metastasis ; Microscopy, Fluorescence ; Middle Aged ; multidisciplinary ; Neoadjuvant Therapy ; Neoplasm Recurrence, Local - blood ; Neoplasm Recurrence, Local - pathology ; Neoplasm, Residual - blood ; Neoplasm, Residual - drug therapy ; Neoplastic Cells, Circulating - pathology ; Patients ; Prognosis ; Receptor, ErbB-2 - metabolism ; Recurrence ; Regulatory approval ; Science ; Science (multidisciplinary) ; Treatment Outcome ; Triple Negative Breast Neoplasms - blood ; Triple Negative Breast Neoplasms - drug therapy</subject><ispartof>Scientific reports, 2020-10, Vol.10 (1), p.17466-17466, Article 17466</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. 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A total of 173, non-metastatic breast cancer patients treated with NCT were prospectively enrolled. CTCs were obtained from blood drawn pre-NCT and post-NCT using a SMART BIOPSY SYSTEM isolation kit (Cytogen Inc., Seoul, Korea) with immunofluorescence staining. Excluding 26 HER2-positive patients, Relapse-free survival (RFS) and overall survival (OS) related to the CTC count and the association of the CTC count with the treatment response to given therapy were analyzed in 147 HER2-negative patients. Among 147 HER2-negative patients, 28 relapses (19.0%) and 13 deaths (8.8%, all breast cancer-specific) were observed during a median follow-up of 37.3 months. One hundred and seven patients (72.8%) were hormone receptor-positive, and 40 patients (27.2%) had triple-negative breast cancer (TNBC). One or more CTCs were identified in 88 of the 147 patients (59.9%) before NCT and 77 of the 134 patients (52.4%) after NCT. In the entire HER2-negative patient cohort, the initial nodal status was the most significant factor influencing RFS and OS. In TNBC, 11 patients (27.5%) achieved pCR and patients that failed to achieve pCR with ≥ 5 CTCs after NCT, showed worse RFS (HR, 10.66; 95% CI, 1.80–63.07; p  = 0.009) and OS (HR, 14.00; 95% CI, 1.26–155.53; p  = 0.032). The patients with residual tumor and a high number of the CTCs after NCT displayed the worse outcome. These findings could provide justification to launch a future, well designed trial with longer follow-up data to obtain regulatory approval for clinical use of the assay, especially for the ER-positive, HER2-negative breast cancer subset.</description><subject>631/67/1347</subject><subject>631/67/1857</subject><subject>692/4028/67/1347</subject><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Biopsy</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - blood</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Cancer therapies</subject><subject>Cell Count</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Disease-Free Survival</subject><subject>ErbB-2 protein</subject><subject>Estrogen Receptor alpha - metabolism</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Immunofluorescence</subject><subject>MCF-7 Cells</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Microscopy, Fluorescence</subject><subject>Middle Aged</subject><subject>multidisciplinary</subject><subject>Neoadjuvant Therapy</subject><subject>Neoplasm Recurrence, Local - blood</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm, Residual - blood</subject><subject>Neoplasm, Residual - drug therapy</subject><subject>Neoplastic Cells, Circulating - pathology</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Recurrence</subject><subject>Regulatory approval</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Treatment Outcome</subject><subject>Triple Negative Breast Neoplasms - blood</subject><subject>Triple Negative Breast Neoplasms - drug therapy</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kUtP3TAQha2qqKALf4BFZambbtKOX0m8qYRQXxJSN2VtGWfC9VUSp3YMuv8ep5dS2gXe2Dr-5ow9h5BzBh8YiPZjkkzptgIOVSNV01T3r8gJB6kqLjh__ex8TM5S2kFZimvJ9BtyLATU0NTtCRkvJjvsk0809HTZIk0YvR2o89HlwS5-uqVLHkOkDocihzwttMtx1ScMttvlO1skt8UxlPpo5z31E72JaFOR7eQw0rkY4bSkU3LU2yHh2eO-IddfPv-8_FZd_fj6_fLiqnIK-FL1CoRQIDUohxq56m0jm1qyrhd13wnsQGvdKomyA2ElE8AkthY1Z9K2TGzIp4PvnG9G7FzpHe1g5uhHG_cmWG_-vZn81tyGO9Oomjdlvhvy_tEghl8Z02JGn9YJ2PLpnAyXirVSab32evcfugs5lqkWSqlayZYp9TIFwGrOYKX4gXIxpBSxf3oyA7PGbg6xmxK7-R27uS9Fb59_9qnkT8gFEAcgzWtuGP_2fsH2AZkTuWs</recordid><startdate>20201015</startdate><enddate>20201015</enddate><creator>Gwark, Sungchan</creator><creator>Kim, Jisun</creator><creator>Kwon, Nak-Jung</creator><creator>Kim, Kyoung-Yeon</creator><creator>Kim, YongNam</creator><creator>Lee, Cham Han</creator><creator>Kim, Young Hun</creator><creator>Kim, Myoung Shin</creator><creator>Hong, Sung Woo</creator><creator>Choi, Mi Young</creator><creator>Jeon, Byung Hee</creator><creator>Chang, Suhwan</creator><creator>Yu, Jonghan</creator><creator>Park, Ji Yeon</creator><creator>Lee, Hee Jin</creator><creator>Lee, Sae Byul</creator><creator>Chung, Il Yong</creator><creator>Ko, Beom Seok</creator><creator>Kim, Hee Jeong</creator><creator>Lee, Jong Won</creator><creator>Son, Byung Ho</creator><creator>Ahn, Jin-Hee</creator><creator>Jung, Kyung Hae</creator><creator>Kim, Sung-Bae</creator><creator>Gong, Gyung-Yub</creator><creator>Ahn, Sei Hyun</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</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>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5271-8530</orcidid><orcidid>https://orcid.org/0000-0002-4963-6603</orcidid><orcidid>https://orcid.org/0000-0002-6757-0388</orcidid><orcidid>https://orcid.org/0000-0002-4884-6107</orcidid><orcidid>https://orcid.org/0000-0001-7875-1603</orcidid></search><sort><creationdate>20201015</creationdate><title>Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients</title><author>Gwark, Sungchan ; Kim, Jisun ; Kwon, Nak-Jung ; Kim, Kyoung-Yeon ; Kim, YongNam ; Lee, Cham Han ; Kim, Young Hun ; Kim, Myoung Shin ; Hong, Sung Woo ; Choi, Mi Young ; Jeon, Byung Hee ; Chang, Suhwan ; Yu, Jonghan ; Park, Ji Yeon ; Lee, Hee Jin ; Lee, Sae Byul ; Chung, Il Yong ; Ko, Beom Seok ; Kim, Hee Jeong ; Lee, Jong Won ; Son, Byung Ho ; Ahn, Jin-Hee ; Jung, Kyung Hae ; Kim, Sung-Bae ; Gong, Gyung-Yub ; Ahn, Sei Hyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c502t-f5033504905ce9e25fa747641df36fd3ed0999854e4d03a413014e8ae9214a813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>631/67/1347</topic><topic>631/67/1857</topic><topic>692/4028/67/1347</topic><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Biopsy</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - blood</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Cancer therapies</topic><topic>Cell Count</topic><topic>Chemotherapy</topic><topic>Chemotherapy, Adjuvant</topic><topic>Disease-Free Survival</topic><topic>ErbB-2 protein</topic><topic>Estrogen Receptor alpha - metabolism</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Immunofluorescence</topic><topic>MCF-7 Cells</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Microscopy, Fluorescence</topic><topic>Middle Aged</topic><topic>multidisciplinary</topic><topic>Neoadjuvant Therapy</topic><topic>Neoplasm Recurrence, Local - blood</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm, Residual - blood</topic><topic>Neoplasm, Residual - drug therapy</topic><topic>Neoplastic Cells, Circulating - pathology</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Recurrence</topic><topic>Regulatory approval</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Treatment Outcome</topic><topic>Triple Negative Breast Neoplasms - blood</topic><topic>Triple Negative Breast Neoplasms - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gwark, Sungchan</creatorcontrib><creatorcontrib>Kim, Jisun</creatorcontrib><creatorcontrib>Kwon, Nak-Jung</creatorcontrib><creatorcontrib>Kim, Kyoung-Yeon</creatorcontrib><creatorcontrib>Kim, YongNam</creatorcontrib><creatorcontrib>Lee, Cham Han</creatorcontrib><creatorcontrib>Kim, Young Hun</creatorcontrib><creatorcontrib>Kim, Myoung Shin</creatorcontrib><creatorcontrib>Hong, Sung Woo</creatorcontrib><creatorcontrib>Choi, Mi Young</creatorcontrib><creatorcontrib>Jeon, Byung Hee</creatorcontrib><creatorcontrib>Chang, Suhwan</creatorcontrib><creatorcontrib>Yu, Jonghan</creatorcontrib><creatorcontrib>Park, Ji Yeon</creatorcontrib><creatorcontrib>Lee, Hee Jin</creatorcontrib><creatorcontrib>Lee, Sae Byul</creatorcontrib><creatorcontrib>Chung, Il Yong</creatorcontrib><creatorcontrib>Ko, Beom Seok</creatorcontrib><creatorcontrib>Kim, Hee Jeong</creatorcontrib><creatorcontrib>Lee, Jong Won</creatorcontrib><creatorcontrib>Son, Byung Ho</creatorcontrib><creatorcontrib>Ahn, Jin-Hee</creatorcontrib><creatorcontrib>Jung, Kyung Hae</creatorcontrib><creatorcontrib>Kim, Sung-Bae</creatorcontrib><creatorcontrib>Gong, Gyung-Yub</creatorcontrib><creatorcontrib>Ahn, Sei Hyun</creatorcontrib><collection>Springer Nature OA Free Journals</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>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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 One Sustainability</collection><collection>ProQuest Central UK/Ireland</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>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gwark, Sungchan</au><au>Kim, Jisun</au><au>Kwon, Nak-Jung</au><au>Kim, Kyoung-Yeon</au><au>Kim, YongNam</au><au>Lee, Cham Han</au><au>Kim, Young Hun</au><au>Kim, Myoung Shin</au><au>Hong, Sung Woo</au><au>Choi, Mi Young</au><au>Jeon, Byung Hee</au><au>Chang, Suhwan</au><au>Yu, Jonghan</au><au>Park, Ji Yeon</au><au>Lee, Hee Jin</au><au>Lee, Sae Byul</au><au>Chung, Il Yong</au><au>Ko, Beom Seok</au><au>Kim, Hee Jeong</au><au>Lee, Jong Won</au><au>Son, Byung Ho</au><au>Ahn, Jin-Hee</au><au>Jung, Kyung Hae</au><au>Kim, Sung-Bae</au><au>Gong, Gyung-Yub</au><au>Ahn, Sei Hyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-10-15</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>17466</spage><epage>17466</epage><pages>17466-17466</pages><artnum>17466</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>We evaluated the prognostic implications of the circulating tumor cell (CTC) count in non-metastatic, HER2-negative breast cancer patients who failed to achieve pathologic complete response (pCR) after neoadjuvant chemotherapy (NCT). A total of 173, non-metastatic breast cancer patients treated with NCT were prospectively enrolled. CTCs were obtained from blood drawn pre-NCT and post-NCT using a SMART BIOPSY SYSTEM isolation kit (Cytogen Inc., Seoul, Korea) with immunofluorescence staining. Excluding 26 HER2-positive patients, Relapse-free survival (RFS) and overall survival (OS) related to the CTC count and the association of the CTC count with the treatment response to given therapy were analyzed in 147 HER2-negative patients. Among 147 HER2-negative patients, 28 relapses (19.0%) and 13 deaths (8.8%, all breast cancer-specific) were observed during a median follow-up of 37.3 months. One hundred and seven patients (72.8%) were hormone receptor-positive, and 40 patients (27.2%) had triple-negative breast cancer (TNBC). One or more CTCs were identified in 88 of the 147 patients (59.9%) before NCT and 77 of the 134 patients (52.4%) after NCT. In the entire HER2-negative patient cohort, the initial nodal status was the most significant factor influencing RFS and OS. In TNBC, 11 patients (27.5%) achieved pCR and patients that failed to achieve pCR with ≥ 5 CTCs after NCT, showed worse RFS (HR, 10.66; 95% CI, 1.80–63.07; p  = 0.009) and OS (HR, 14.00; 95% CI, 1.26–155.53; p  = 0.032). The patients with residual tumor and a high number of the CTCs after NCT displayed the worse outcome. These findings could provide justification to launch a future, well designed trial with longer follow-up data to obtain regulatory approval for clinical use of the assay, especially for the ER-positive, HER2-negative breast cancer subset.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33060768</pmid><doi>10.1038/s41598-020-74577-w</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-5271-8530</orcidid><orcidid>https://orcid.org/0000-0002-4963-6603</orcidid><orcidid>https://orcid.org/0000-0002-6757-0388</orcidid><orcidid>https://orcid.org/0000-0002-4884-6107</orcidid><orcidid>https://orcid.org/0000-0001-7875-1603</orcidid><oa>free_for_read</oa></addata></record>
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subjects 631/67/1347
631/67/1857
692/4028/67/1347
Adult
Aged
Biomarkers, Tumor - metabolism
Biopsy
Breast cancer
Breast Neoplasms - blood
Breast Neoplasms - drug therapy
Cancer therapies
Cell Count
Chemotherapy
Chemotherapy, Adjuvant
Disease-Free Survival
ErbB-2 protein
Estrogen Receptor alpha - metabolism
Female
Follow-Up Studies
Humanities and Social Sciences
Humans
Immunofluorescence
MCF-7 Cells
Metastases
Metastasis
Microscopy, Fluorescence
Middle Aged
multidisciplinary
Neoadjuvant Therapy
Neoplasm Recurrence, Local - blood
Neoplasm Recurrence, Local - pathology
Neoplasm, Residual - blood
Neoplasm, Residual - drug therapy
Neoplastic Cells, Circulating - pathology
Patients
Prognosis
Receptor, ErbB-2 - metabolism
Recurrence
Regulatory approval
Science
Science (multidisciplinary)
Treatment Outcome
Triple Negative Breast Neoplasms - blood
Triple Negative Breast Neoplasms - drug therapy
title Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients
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