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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7562710</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2451845991</sourcerecordid><originalsourceid>FETCH-LOGICAL-c502t-f5033504905ce9e25fa747641df36fd3ed0999854e4d03a413014e8ae9214a813</originalsourceid><addsrcrecordid>eNp9kUtP3TAQha2qqKALf4BFZambbtKOX0m8qYRQXxJSN2VtGWfC9VUSp3YMuv8ep5dS2gXe2Dr-5ow9h5BzBh8YiPZjkkzptgIOVSNV01T3r8gJB6kqLjh__ex8TM5S2kFZimvJ9BtyLATU0NTtCRkvJjvsk0809HTZIk0YvR2o89HlwS5-uqVLHkOkDocihzwttMtx1ScMttvlO1skt8UxlPpo5z31E72JaFOR7eQw0rkY4bSkU3LU2yHh2eO-IddfPv-8_FZd_fj6_fLiqnIK-FL1CoRQIDUohxq56m0jm1qyrhd13wnsQGvdKomyA2ElE8AkthY1Z9K2TGzIp4PvnG9G7FzpHe1g5uhHG_cmWG_-vZn81tyGO9Oomjdlvhvy_tEghl8Z02JGn9YJ2PLpnAyXirVSab32evcfugs5lqkWSqlayZYp9TIFwGrOYKX4gXIxpBSxf3oyA7PGbg6xmxK7-R27uS9Fb59_9qnkT8gFEAcgzWtuGP_2fsH2AZkTuWs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2500162105</pqid></control><display><type>article</type><title>Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients</title><source>MEDLINE</source><source>Nature Free</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature OA Free Journals</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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. This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c502t-f5033504905ce9e25fa747641df36fd3ed0999854e4d03a413014e8ae9214a813</citedby><cites>FETCH-LOGICAL-c502t-f5033504905ce9e25fa747641df36fd3ed0999854e4d03a413014e8ae9214a813</cites><orcidid>0000-0001-5271-8530 ; 0000-0002-4963-6603 ; 0000-0002-6757-0388 ; 0000-0002-4884-6107 ; 0000-0001-7875-1603</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562710/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562710/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33060768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><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.</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 & 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 & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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> |
fulltext | fulltext |
identifier | ISSN: 2045-2322 |
ispartof | Scientific reports, 2020-10, Vol.10 (1), p.17466-17466, Article 17466 |
issn | 2045-2322 2045-2322 |
language | eng |
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source | MEDLINE; Nature Free; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry; Springer Nature OA Free Journals |
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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