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Preoperative inflammation markers and IDH mutation status predict glioblastoma patient survival
Recent studies suggest that inflammation response biomarkers are prognostic indicators of solid tumor outcomes. Here, we quantify the prognostic value of the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR) in glioblastomas (GBMs), taki...
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Published in: | Oncotarget 2017-07, Vol.8 (30), p.50117-50123 |
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description | Recent studies suggest that inflammation response biomarkers are prognostic indicators of solid tumor outcomes. Here, we quantify the prognostic value of the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR) in glioblastomas (GBMs), taking into consideration the role of the isocitrate dehydrogenase (IDH) mutation status. We examined 141 primary glioblastomas (pGBMs) and 25 secondary glioblastomas (sGBMs). NLRs, PLRs, and LMRs were calculated before surgery. IDH mutations were detected immunohistochemically after tumor resection, and patients' clinical outcomes were analyzed after classification into GBM, pGBM, and IDH-wild type glioblastoma (IDH-wt GBM) groups. To make comparisons, we set cutoffs for NLR, PLR and LMR of 4.0, 175.0, and 3.7, respectively. In a multivariate analysis, both NLR (HR=1.712, 95% CI 1.026-2.858, p=0.040) and PLR (HR=2.051, 95% CI 1.288-3.267, p=0.002) had independent prognostic value. While a low NLR was associated with a better prognosis only in the IDH-wt GBM group, PLR was predictive of patient survival in the GBM, pGBM, and IDH-wt GBM groups. By contrast, LMR exhibited no prognostic value for any of the 3 types of GBM. |
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Here, we quantify the prognostic value of the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR) in glioblastomas (GBMs), taking into consideration the role of the isocitrate dehydrogenase (IDH) mutation status. We examined 141 primary glioblastomas (pGBMs) and 25 secondary glioblastomas (sGBMs). NLRs, PLRs, and LMRs were calculated before surgery. IDH mutations were detected immunohistochemically after tumor resection, and patients' clinical outcomes were analyzed after classification into GBM, pGBM, and IDH-wild type glioblastoma (IDH-wt GBM) groups. To make comparisons, we set cutoffs for NLR, PLR and LMR of 4.0, 175.0, and 3.7, respectively. In a multivariate analysis, both NLR (HR=1.712, 95% CI 1.026-2.858, p=0.040) and PLR (HR=2.051, 95% CI 1.288-3.267, p=0.002) had independent prognostic value. While a low NLR was associated with a better prognosis only in the IDH-wt GBM group, PLR was predictive of patient survival in the GBM, pGBM, and IDH-wt GBM groups. By contrast, LMR exhibited no prognostic value for any of the 3 types of GBM.</description><identifier>ISSN: 1949-2553</identifier><identifier>EISSN: 1949-2553</identifier><identifier>DOI: 10.18632/oncotarget.15235</identifier><identifier>PMID: 28223536</identifier><language>eng</language><publisher>United States: Impact Journals LLC</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor ; Clinical Research Paper ; Female ; Glioblastoma - genetics ; Glioblastoma - mortality ; Glioblastoma - pathology ; Humans ; Inflammation - metabolism ; Isocitrate Dehydrogenase - metabolism ; Lymphocytes - pathology ; Male ; Middle Aged ; Monocytes - pathology ; Mutation ; Neutrophils - pathology ; Preoperative Period ; Survival Analysis ; Young Adult</subject><ispartof>Oncotarget, 2017-07, Vol.8 (30), p.50117-50123</ispartof><rights>Copyright: © 2017 Wang et al. 2017</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-d545b41aff95fa5fb0540d66fadb09485f1e7531708ec045b4a5817ce4f896953</citedby><cites>FETCH-LOGICAL-c356t-d545b41aff95fa5fb0540d66fadb09485f1e7531708ec045b4a5817ce4f896953</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/PMC5564834/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5564834/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28223536$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Peng-Fei</creatorcontrib><creatorcontrib>Song, Hong-Wang</creatorcontrib><creatorcontrib>Cai, Hong-Qing</creatorcontrib><creatorcontrib>Kong, Ling-Wei</creatorcontrib><creatorcontrib>Yao, Kun</creatorcontrib><creatorcontrib>Jiang, Tao</creatorcontrib><creatorcontrib>Li, Shou-Wei</creatorcontrib><creatorcontrib>Yan, Chang-Xiang</creatorcontrib><title>Preoperative inflammation markers and IDH mutation status predict glioblastoma patient survival</title><title>Oncotarget</title><addtitle>Oncotarget</addtitle><description>Recent studies suggest that inflammation response biomarkers are prognostic indicators of solid tumor outcomes. Here, we quantify the prognostic value of the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR) in glioblastomas (GBMs), taking into consideration the role of the isocitrate dehydrogenase (IDH) mutation status. We examined 141 primary glioblastomas (pGBMs) and 25 secondary glioblastomas (sGBMs). NLRs, PLRs, and LMRs were calculated before surgery. IDH mutations were detected immunohistochemically after tumor resection, and patients' clinical outcomes were analyzed after classification into GBM, pGBM, and IDH-wild type glioblastoma (IDH-wt GBM) groups. To make comparisons, we set cutoffs for NLR, PLR and LMR of 4.0, 175.0, and 3.7, respectively. In a multivariate analysis, both NLR (HR=1.712, 95% CI 1.026-2.858, p=0.040) and PLR (HR=2.051, 95% CI 1.288-3.267, p=0.002) had independent prognostic value. While a low NLR was associated with a better prognosis only in the IDH-wt GBM group, PLR was predictive of patient survival in the GBM, pGBM, and IDH-wt GBM groups. By contrast, LMR exhibited no prognostic value for any of the 3 types of GBM.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers, Tumor</subject><subject>Clinical Research Paper</subject><subject>Female</subject><subject>Glioblastoma - genetics</subject><subject>Glioblastoma - mortality</subject><subject>Glioblastoma - pathology</subject><subject>Humans</subject><subject>Inflammation - metabolism</subject><subject>Isocitrate Dehydrogenase - metabolism</subject><subject>Lymphocytes - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Monocytes - pathology</subject><subject>Mutation</subject><subject>Neutrophils - pathology</subject><subject>Preoperative Period</subject><subject>Survival Analysis</subject><subject>Young Adult</subject><issn>1949-2553</issn><issn>1949-2553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVUctOwzAQtBCIVqUfwAX5yKXFjuPEuSCh8mglJDjA2XISuxicONhOJP4e05ZS9rJr7czsWAPAOUZzzDKSXNm2skG4tQxzTBNCj8AYF2kxSyglxwfzCEy9f0exaJqzpDgFo4QlkUCyMeDPTtpOOhH0IKFulRFNEx-2hY1wH9J5KNoarm6XsOnDduFj7z3snKx1FeDaaFsa4YNtBOwiRLYB-t4NehDmDJwoYbyc7voEvN7fvSyWs8enh9Xi5nFWEZqFWU1TWqZYKFVQJagqo1dUZ5kSdYmKlFGFZU4JzhGTFfrBCspwXslUsSIrKJmA661u15eNrKvowQnDO6fjN764FZr_37T6ja_twCnNUkbSKHC5E3D2s5c-8Eb7ShojWml7zzHLUcEyjFCE4i20ctZ7J9X-DEZ8kw3_y4Zvsomci0N_e8ZvEuQbzlCQdw</recordid><startdate>20170725</startdate><enddate>20170725</enddate><creator>Wang, Peng-Fei</creator><creator>Song, Hong-Wang</creator><creator>Cai, Hong-Qing</creator><creator>Kong, Ling-Wei</creator><creator>Yao, Kun</creator><creator>Jiang, Tao</creator><creator>Li, Shou-Wei</creator><creator>Yan, Chang-Xiang</creator><general>Impact Journals LLC</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>20170725</creationdate><title>Preoperative inflammation markers and IDH mutation status predict glioblastoma patient survival</title><author>Wang, Peng-Fei ; Song, Hong-Wang ; Cai, Hong-Qing ; Kong, Ling-Wei ; Yao, Kun ; Jiang, Tao ; Li, Shou-Wei ; Yan, Chang-Xiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-d545b41aff95fa5fb0540d66fadb09485f1e7531708ec045b4a5817ce4f896953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers, Tumor</topic><topic>Clinical Research Paper</topic><topic>Female</topic><topic>Glioblastoma - genetics</topic><topic>Glioblastoma - mortality</topic><topic>Glioblastoma - pathology</topic><topic>Humans</topic><topic>Inflammation - metabolism</topic><topic>Isocitrate Dehydrogenase - metabolism</topic><topic>Lymphocytes - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Monocytes - pathology</topic><topic>Mutation</topic><topic>Neutrophils - pathology</topic><topic>Preoperative Period</topic><topic>Survival Analysis</topic><topic>Young Adult</topic><toplevel>online_resources</toplevel><creatorcontrib>Wang, Peng-Fei</creatorcontrib><creatorcontrib>Song, Hong-Wang</creatorcontrib><creatorcontrib>Cai, Hong-Qing</creatorcontrib><creatorcontrib>Kong, Ling-Wei</creatorcontrib><creatorcontrib>Yao, Kun</creatorcontrib><creatorcontrib>Jiang, Tao</creatorcontrib><creatorcontrib>Li, Shou-Wei</creatorcontrib><creatorcontrib>Yan, Chang-Xiang</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>Oncotarget</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Peng-Fei</au><au>Song, Hong-Wang</au><au>Cai, Hong-Qing</au><au>Kong, Ling-Wei</au><au>Yao, Kun</au><au>Jiang, Tao</au><au>Li, Shou-Wei</au><au>Yan, Chang-Xiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preoperative inflammation markers and IDH mutation status predict glioblastoma patient survival</atitle><jtitle>Oncotarget</jtitle><addtitle>Oncotarget</addtitle><date>2017-07-25</date><risdate>2017</risdate><volume>8</volume><issue>30</issue><spage>50117</spage><epage>50123</epage><pages>50117-50123</pages><issn>1949-2553</issn><eissn>1949-2553</eissn><abstract>Recent studies suggest that inflammation response biomarkers are prognostic indicators of solid tumor outcomes. Here, we quantify the prognostic value of the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR) in glioblastomas (GBMs), taking into consideration the role of the isocitrate dehydrogenase (IDH) mutation status. We examined 141 primary glioblastomas (pGBMs) and 25 secondary glioblastomas (sGBMs). NLRs, PLRs, and LMRs were calculated before surgery. IDH mutations were detected immunohistochemically after tumor resection, and patients' clinical outcomes were analyzed after classification into GBM, pGBM, and IDH-wild type glioblastoma (IDH-wt GBM) groups. To make comparisons, we set cutoffs for NLR, PLR and LMR of 4.0, 175.0, and 3.7, respectively. In a multivariate analysis, both NLR (HR=1.712, 95% CI 1.026-2.858, p=0.040) and PLR (HR=2.051, 95% CI 1.288-3.267, p=0.002) had independent prognostic value. While a low NLR was associated with a better prognosis only in the IDH-wt GBM group, PLR was predictive of patient survival in the GBM, pGBM, and IDH-wt GBM groups. By contrast, LMR exhibited no prognostic value for any of the 3 types of GBM.</abstract><cop>United States</cop><pub>Impact Journals LLC</pub><pmid>28223536</pmid><doi>10.18632/oncotarget.15235</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Biomarkers, Tumor Clinical Research Paper Female Glioblastoma - genetics Glioblastoma - mortality Glioblastoma - pathology Humans Inflammation - metabolism Isocitrate Dehydrogenase - metabolism Lymphocytes - pathology Male Middle Aged Monocytes - pathology Mutation Neutrophils - pathology Preoperative Period Survival Analysis Young Adult |
title | Preoperative inflammation markers and IDH mutation status predict glioblastoma patient survival |
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