Prediction of the preoperative chemoradiotherapy response for rectal cancer by peripheral blood lymphocyte subsets
Although neoadjuvant chemoradiotherapy (CRT) has become a standard procedure to downstage locally advanced rectal cancer prior to surgery, markers to predict the response to CRT have not been fully identified. The aim of this study was to identify predictive factors of response to CRT, especially fo...
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Veröffentlicht in: | World journal of surgical oncology 2015-02, Vol.13 (1), p.30-30, Article 30 |
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creator | Tada, Noriko Kawai, Kazushige Tsuno, Nelson H Ishihara, Soichiro Yamaguchi, Hironori Sunami, Eiji Kitayama, Joji Oba, Koji Watanabe, Toshiaki |
description | Although neoadjuvant chemoradiotherapy (CRT) has become a standard procedure to downstage locally advanced rectal cancer prior to surgery, markers to predict the response to CRT have not been fully identified. The aim of this study was to identify predictive factors of response to CRT, especially focusing on peripheral blood leukocyte subsets.
A total of 45 consecutive patients diagnosed with primary rectal cancer were prospectively enrolled and received CRT followed by curative resection. The numbers of each lymphocyte subset in peripheral blood pre- and post-CRT were analyzed using flow cytometry. According to the pathological response to CRT, patients were classified into high (Hi-R) and low (Lo-R) response groups.
Hi-R cases had significantly higher numbers of pre-CRT lymphocytes (p = 0.018), T lymphocytes (p = 0.009) and helper T lymphocytes (Th lymphocytes, p = 0.015) compared to the Lo-R cases. With the receiver-operating characteristic curve for numbers of pre-CRT T lymphocytes, the area under the curve (AUC) was 0.733, and the optimal cutoff value was 1196/μl, with 76.5% sensitivity, 67.8% specificity, 59.1% positive and 82.6% negative predictive values. The numbers of pre-CRT Th lymphocytes and cytotoxic lymphocytes were both independent predictors of the high CRT response in the multivariate analysis.
In addition to the direct cytotoxicity of CRT, recent studies have demonstrated the induction of an immunological host response, which also contributed to the tumor regression induced by CRT. Our result suggested the potential role of circulating T lymphocytes in predicting the response to CRT in colorectal cancer patients. |
doi_str_mv | 10.1186/s12957-014-0418-0 |
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A total of 45 consecutive patients diagnosed with primary rectal cancer were prospectively enrolled and received CRT followed by curative resection. The numbers of each lymphocyte subset in peripheral blood pre- and post-CRT were analyzed using flow cytometry. According to the pathological response to CRT, patients were classified into high (Hi-R) and low (Lo-R) response groups.
Hi-R cases had significantly higher numbers of pre-CRT lymphocytes (p = 0.018), T lymphocytes (p = 0.009) and helper T lymphocytes (Th lymphocytes, p = 0.015) compared to the Lo-R cases. With the receiver-operating characteristic curve for numbers of pre-CRT T lymphocytes, the area under the curve (AUC) was 0.733, and the optimal cutoff value was 1196/μl, with 76.5% sensitivity, 67.8% specificity, 59.1% positive and 82.6% negative predictive values. The numbers of pre-CRT Th lymphocytes and cytotoxic lymphocytes were both independent predictors of the high CRT response in the multivariate analysis.
In addition to the direct cytotoxicity of CRT, recent studies have demonstrated the induction of an immunological host response, which also contributed to the tumor regression induced by CRT. Our result suggested the potential role of circulating T lymphocytes in predicting the response to CRT in colorectal cancer patients.</description><identifier>ISSN: 1477-7819</identifier><identifier>EISSN: 1477-7819</identifier><identifier>DOI: 10.1186/s12957-014-0418-0</identifier><identifier>PMID: 25890185</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adenocarcinoma - secondary ; Adenocarcinoma - therapy ; Adenocarcinoma, Mucinous - secondary ; Adenocarcinoma, Mucinous - therapy ; Adult ; Aged ; Aged, 80 and over ; Analysis ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Area Under Curve ; B cells ; Cancer ; Care and treatment ; Chemoradiotherapy ; Colorectal cancer ; Female ; Follow-Up Studies ; Health aspects ; Humans ; Lymphatic Metastasis ; Lymphocyte Subsets - pathology ; Male ; Medical equipment and supplies industry ; Medical test kit industry ; Middle Aged ; Multivariate Analysis ; Neoadjuvant Therapy ; Neoplasm Invasiveness ; Neoplasm Staging ; Prognosis ; Prospective Studies ; Rectal Neoplasms - pathology ; Rectal Neoplasms - therapy ; ROC Curve ; Survival Rate ; T cells</subject><ispartof>World journal of surgical oncology, 2015-02, Vol.13 (1), p.30-30, Article 30</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Tada et al.; licensee BioMed Central. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b624t-8174176113bd08e9ca7d01b77b8bd076216996d884853b83d5586a3d8c5338053</citedby><cites>FETCH-LOGICAL-b624t-8174176113bd08e9ca7d01b77b8bd076216996d884853b83d5586a3d8c5338053</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/PMC4327968/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327968/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25890185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tada, Noriko</creatorcontrib><creatorcontrib>Kawai, Kazushige</creatorcontrib><creatorcontrib>Tsuno, Nelson H</creatorcontrib><creatorcontrib>Ishihara, Soichiro</creatorcontrib><creatorcontrib>Yamaguchi, Hironori</creatorcontrib><creatorcontrib>Sunami, Eiji</creatorcontrib><creatorcontrib>Kitayama, Joji</creatorcontrib><creatorcontrib>Oba, Koji</creatorcontrib><creatorcontrib>Watanabe, Toshiaki</creatorcontrib><title>Prediction of the preoperative chemoradiotherapy response for rectal cancer by peripheral blood lymphocyte subsets</title><title>World journal of surgical oncology</title><addtitle>World J Surg Oncol</addtitle><description>Although neoadjuvant chemoradiotherapy (CRT) has become a standard procedure to downstage locally advanced rectal cancer prior to surgery, markers to predict the response to CRT have not been fully identified. The aim of this study was to identify predictive factors of response to CRT, especially focusing on peripheral blood leukocyte subsets.
A total of 45 consecutive patients diagnosed with primary rectal cancer were prospectively enrolled and received CRT followed by curative resection. The numbers of each lymphocyte subset in peripheral blood pre- and post-CRT were analyzed using flow cytometry. According to the pathological response to CRT, patients were classified into high (Hi-R) and low (Lo-R) response groups.
Hi-R cases had significantly higher numbers of pre-CRT lymphocytes (p = 0.018), T lymphocytes (p = 0.009) and helper T lymphocytes (Th lymphocytes, p = 0.015) compared to the Lo-R cases. With the receiver-operating characteristic curve for numbers of pre-CRT T lymphocytes, the area under the curve (AUC) was 0.733, and the optimal cutoff value was 1196/μl, with 76.5% sensitivity, 67.8% specificity, 59.1% positive and 82.6% negative predictive values. The numbers of pre-CRT Th lymphocytes and cytotoxic lymphocytes were both independent predictors of the high CRT response in the multivariate analysis.
In addition to the direct cytotoxicity of CRT, recent studies have demonstrated the induction of an immunological host response, which also contributed to the tumor regression induced by CRT. Our result suggested the potential role of circulating T lymphocytes in predicting the response to CRT in colorectal cancer patients.</description><subject>Adenocarcinoma - secondary</subject><subject>Adenocarcinoma - therapy</subject><subject>Adenocarcinoma, Mucinous - secondary</subject><subject>Adenocarcinoma, Mucinous - therapy</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Analysis</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Area Under Curve</subject><subject>B cells</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Chemoradiotherapy</subject><subject>Colorectal cancer</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Lymphatic Metastasis</subject><subject>Lymphocyte Subsets - pathology</subject><subject>Male</subject><subject>Medical equipment and supplies industry</subject><subject>Medical test kit industry</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Neoadjuvant Therapy</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Staging</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Rectal Neoplasms - pathology</subject><subject>Rectal Neoplasms - therapy</subject><subject>ROC Curve</subject><subject>Survival Rate</subject><subject>T cells</subject><issn>1477-7819</issn><issn>1477-7819</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1Ustq3TAQNaWlebQf0E0RFEI2TiXr6U0hpE8ItIt2LWR5HKvIlivZAf99ZZyGeyFFC2lmzjnM6ExRvCH4ihAl3idS1VyWmLASM6JK_Kw4JUzKUipSPz94nxRnKf3GuKKU05fFScVVjYnip0X8EaF1dnZhRKFDcw9oihAmiGZ294BsD0OIpnUhl6KZVhQhTWFMgLoQc2Bn45E1o4WImhVlops2pEeND6FFfh2mPth1BpSWJsGcXhUvOuMTvH64z4tfnz_9vPla3n7_8u3m-rZsRMXmUhHJiBSE0KbFCmprZItJI2WjckKKioi6Fq1STHHaKNpyroShrbKcUoU5PS8-7LrT0gzQWhjn3JaeohtMXHUwTh9XRtfru3CvGa1kLVQW-LgLNC78R-C4YsOgd0909kRvnmicZS4f-ojhzwJp1oNLFrw3I4QlaSIkE6rmimXoux16ZzxoN3Yh69oNrq85Ixxn-7bBrp5A5dPC4GwYoXM5f0S4OCD0YPzcp-CXzfV0DCQ70MaQUoTucViC9bZyT4739vCbHxn_doz-BRBy0sE</recordid><startdate>20150207</startdate><enddate>20150207</enddate><creator>Tada, Noriko</creator><creator>Kawai, Kazushige</creator><creator>Tsuno, Nelson H</creator><creator>Ishihara, Soichiro</creator><creator>Yamaguchi, Hironori</creator><creator>Sunami, Eiji</creator><creator>Kitayama, Joji</creator><creator>Oba, Koji</creator><creator>Watanabe, Toshiaki</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150207</creationdate><title>Prediction of the preoperative chemoradiotherapy response for rectal cancer by peripheral blood lymphocyte subsets</title><author>Tada, Noriko ; Kawai, Kazushige ; Tsuno, Nelson H ; Ishihara, Soichiro ; Yamaguchi, Hironori ; Sunami, Eiji ; Kitayama, Joji ; Oba, Koji ; Watanabe, Toshiaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b624t-8174176113bd08e9ca7d01b77b8bd076216996d884853b83d5586a3d8c5338053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adenocarcinoma - secondary</topic><topic>Adenocarcinoma - therapy</topic><topic>Adenocarcinoma, Mucinous - secondary</topic><topic>Adenocarcinoma, Mucinous - therapy</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Analysis</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Area Under Curve</topic><topic>B cells</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Chemoradiotherapy</topic><topic>Colorectal cancer</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Lymphatic Metastasis</topic><topic>Lymphocyte Subsets - pathology</topic><topic>Male</topic><topic>Medical equipment and supplies industry</topic><topic>Medical test kit industry</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Neoadjuvant Therapy</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Staging</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Rectal Neoplasms - pathology</topic><topic>Rectal Neoplasms - therapy</topic><topic>ROC Curve</topic><topic>Survival Rate</topic><topic>T cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tada, Noriko</creatorcontrib><creatorcontrib>Kawai, Kazushige</creatorcontrib><creatorcontrib>Tsuno, Nelson H</creatorcontrib><creatorcontrib>Ishihara, Soichiro</creatorcontrib><creatorcontrib>Yamaguchi, Hironori</creatorcontrib><creatorcontrib>Sunami, Eiji</creatorcontrib><creatorcontrib>Kitayama, Joji</creatorcontrib><creatorcontrib>Oba, Koji</creatorcontrib><creatorcontrib>Watanabe, Toshiaki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tada, Noriko</au><au>Kawai, Kazushige</au><au>Tsuno, Nelson H</au><au>Ishihara, Soichiro</au><au>Yamaguchi, Hironori</au><au>Sunami, Eiji</au><au>Kitayama, Joji</au><au>Oba, Koji</au><au>Watanabe, Toshiaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prediction of the preoperative chemoradiotherapy response for rectal cancer by peripheral blood lymphocyte subsets</atitle><jtitle>World journal of surgical oncology</jtitle><addtitle>World J Surg Oncol</addtitle><date>2015-02-07</date><risdate>2015</risdate><volume>13</volume><issue>1</issue><spage>30</spage><epage>30</epage><pages>30-30</pages><artnum>30</artnum><issn>1477-7819</issn><eissn>1477-7819</eissn><abstract>Although neoadjuvant chemoradiotherapy (CRT) has become a standard procedure to downstage locally advanced rectal cancer prior to surgery, markers to predict the response to CRT have not been fully identified. The aim of this study was to identify predictive factors of response to CRT, especially focusing on peripheral blood leukocyte subsets.
A total of 45 consecutive patients diagnosed with primary rectal cancer were prospectively enrolled and received CRT followed by curative resection. The numbers of each lymphocyte subset in peripheral blood pre- and post-CRT were analyzed using flow cytometry. According to the pathological response to CRT, patients were classified into high (Hi-R) and low (Lo-R) response groups.
Hi-R cases had significantly higher numbers of pre-CRT lymphocytes (p = 0.018), T lymphocytes (p = 0.009) and helper T lymphocytes (Th lymphocytes, p = 0.015) compared to the Lo-R cases. With the receiver-operating characteristic curve for numbers of pre-CRT T lymphocytes, the area under the curve (AUC) was 0.733, and the optimal cutoff value was 1196/μl, with 76.5% sensitivity, 67.8% specificity, 59.1% positive and 82.6% negative predictive values. The numbers of pre-CRT Th lymphocytes and cytotoxic lymphocytes were both independent predictors of the high CRT response in the multivariate analysis.
In addition to the direct cytotoxicity of CRT, recent studies have demonstrated the induction of an immunological host response, which also contributed to the tumor regression induced by CRT. Our result suggested the potential role of circulating T lymphocytes in predicting the response to CRT in colorectal cancer patients.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>25890185</pmid><doi>10.1186/s12957-014-0418-0</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - secondary Adenocarcinoma - therapy Adenocarcinoma, Mucinous - secondary Adenocarcinoma, Mucinous - therapy Adult Aged Aged, 80 and over Analysis Antineoplastic Combined Chemotherapy Protocols - therapeutic use Area Under Curve B cells Cancer Care and treatment Chemoradiotherapy Colorectal cancer Female Follow-Up Studies Health aspects Humans Lymphatic Metastasis Lymphocyte Subsets - pathology Male Medical equipment and supplies industry Medical test kit industry Middle Aged Multivariate Analysis Neoadjuvant Therapy Neoplasm Invasiveness Neoplasm Staging Prognosis Prospective Studies Rectal Neoplasms - pathology Rectal Neoplasms - therapy ROC Curve Survival Rate T cells |
title | Prediction of the preoperative chemoradiotherapy response for rectal cancer by peripheral blood lymphocyte subsets |
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