Prognostic evaluation of patients with resectable lung cancer using systemic inflammatory response parameters
Lung cancer is one of the leading causes of cancer-associated mortality. C-reactive protein (CRP), albumin (ALB), globulin (GLB), lactate dehydrogenase (LDH), neutrophil-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) have been identified as general parameters for systemic inflammatory...
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Veröffentlicht in: | Oncology letters 2019-02, Vol.17 (2), p.2244-2256 |
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creator | Zhu, Jie Lian, Lian Qin, Hualong Wang, Wen-Jie Ren, Rui Xu, Meng-Dan Chen, Kai Duan, Weiming Gong, Fei-Ran Tao, Min Zhi, Qiaoming Wu, Meng-Yao Li, Wei |
description | Lung cancer is one of the leading causes of cancer-associated mortality. C-reactive protein (CRP), albumin (ALB), globulin (GLB), lactate dehydrogenase (LDH), neutrophil-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) have been identified as general parameters for systemic inflammatory response (SIR). Furthermore, these parameters are also associated with tumor development and metastasis. The present study aimed to investigate the predictive values of these SIR parameters in patients with resectable lung cancer. In total, 101 patients with resectable lung cancer were recruited in the present study. The patients were divided into two groups according to the median value of pre-treatment CRP, ALB, GLB, LDH, NLR or PLR values. The post-/pre-treatment ratios were defined as the ratio of pre-treatment blood parameter values and the corresponding values obtained following therapy. A ratio of ≤1.1 indicated that the values were not increased, while a ratio of >1.1 suggested that the values were increased following treatment. Patients with lower pre-treatment ALB levels had poorer overall survival (OS) rates, whereas GLB, LDH, CRP, NLR or PLR levels were not associated with outcomes. Whole course treatment (surgery combined with adjuvant chemotherapy) significantly increased the value of ALB, but decreased the value of NLR, whereas it had no effect on the values of LDH, CRP or PLR. Post-/pre-treatment LDH and PLR were associated with outcomes. Post-/pre-treatment ALB, GLB, CRP and NLR were not associated with outcomes. Multivariate analysis revealed that a low pre-treatment ALB level and increased post-/pre-treatment PLR were independent risk factors affecting OS. The receiver operating characteristic curve analysis demonstrated that an ALB value of 47.850 g/l was considered to be the optimal cut-off value for prognosis; the sensitivity was 28.8% and specificity was 95.9%. It was suggested that the pre-treatment ALB and post-/pre-treatment PLR may be potential prognostic factors in resectable lung cancer. |
doi_str_mv | 10.3892/ol.2018.9858 |
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C-reactive protein (CRP), albumin (ALB), globulin (GLB), lactate dehydrogenase (LDH), neutrophil-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) have been identified as general parameters for systemic inflammatory response (SIR). Furthermore, these parameters are also associated with tumor development and metastasis. The present study aimed to investigate the predictive values of these SIR parameters in patients with resectable lung cancer. In total, 101 patients with resectable lung cancer were recruited in the present study. The patients were divided into two groups according to the median value of pre-treatment CRP, ALB, GLB, LDH, NLR or PLR values. The post-/pre-treatment ratios were defined as the ratio of pre-treatment blood parameter values and the corresponding values obtained following therapy. A ratio of ≤1.1 indicated that the values were not increased, while a ratio of >1.1 suggested that the values were increased following treatment. Patients with lower pre-treatment ALB levels had poorer overall survival (OS) rates, whereas GLB, LDH, CRP, NLR or PLR levels were not associated with outcomes. Whole course treatment (surgery combined with adjuvant chemotherapy) significantly increased the value of ALB, but decreased the value of NLR, whereas it had no effect on the values of LDH, CRP or PLR. Post-/pre-treatment LDH and PLR were associated with outcomes. Post-/pre-treatment ALB, GLB, CRP and NLR were not associated with outcomes. Multivariate analysis revealed that a low pre-treatment ALB level and increased post-/pre-treatment PLR were independent risk factors affecting OS. The receiver operating characteristic curve analysis demonstrated that an ALB value of 47.850 g/l was considered to be the optimal cut-off value for prognosis; the sensitivity was 28.8% and specificity was 95.9%. It was suggested that the pre-treatment ALB and post-/pre-treatment PLR may be potential prognostic factors in resectable lung cancer.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2018.9858</identifier><identifier>PMID: 30675290</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Adjuvant chemotherapy ; Age ; Albumin ; Blood ; Blood platelets ; C-reactive protein ; Cancer metastasis ; Cancer patients ; Cancer therapies ; Care and treatment ; Cellular proteins ; Chemotherapy ; Committees ; Dehydrogenases ; Development and progression ; Gene expression ; Genetic aspects ; Health aspects ; Immune response ; Inflammation ; Lung cancer ; Lymphocytes ; Medical prognosis ; Medical research ; Metastasis ; Mortality ; Neutrophils ; Oncology ; Proteins ; Risk factors ; Surgery ; Tumors</subject><ispartof>Oncology letters, 2019-02, Vol.17 (2), p.2244-2256</ispartof><rights>COPYRIGHT 2019 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2019</rights><rights>Copyright: © Zhu et al. 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-91a5e9caad4bacfbec752d1ba90fec0b87d66150d8c66c4b7db5c497c163a0b03</citedby><cites>FETCH-LOGICAL-c510t-91a5e9caad4bacfbec752d1ba90fec0b87d66150d8c66c4b7db5c497c163a0b03</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/PMC6341870/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341870/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30675290$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Jie</creatorcontrib><creatorcontrib>Lian, Lian</creatorcontrib><creatorcontrib>Qin, Hualong</creatorcontrib><creatorcontrib>Wang, Wen-Jie</creatorcontrib><creatorcontrib>Ren, Rui</creatorcontrib><creatorcontrib>Xu, Meng-Dan</creatorcontrib><creatorcontrib>Chen, Kai</creatorcontrib><creatorcontrib>Duan, Weiming</creatorcontrib><creatorcontrib>Gong, Fei-Ran</creatorcontrib><creatorcontrib>Tao, Min</creatorcontrib><creatorcontrib>Zhi, Qiaoming</creatorcontrib><creatorcontrib>Wu, Meng-Yao</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><title>Prognostic evaluation of patients with resectable lung cancer using systemic inflammatory response parameters</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>Lung cancer is one of the leading causes of cancer-associated mortality. C-reactive protein (CRP), albumin (ALB), globulin (GLB), lactate dehydrogenase (LDH), neutrophil-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) have been identified as general parameters for systemic inflammatory response (SIR). Furthermore, these parameters are also associated with tumor development and metastasis. The present study aimed to investigate the predictive values of these SIR parameters in patients with resectable lung cancer. In total, 101 patients with resectable lung cancer were recruited in the present study. The patients were divided into two groups according to the median value of pre-treatment CRP, ALB, GLB, LDH, NLR or PLR values. The post-/pre-treatment ratios were defined as the ratio of pre-treatment blood parameter values and the corresponding values obtained following therapy. A ratio of ≤1.1 indicated that the values were not increased, while a ratio of >1.1 suggested that the values were increased following treatment. Patients with lower pre-treatment ALB levels had poorer overall survival (OS) rates, whereas GLB, LDH, CRP, NLR or PLR levels were not associated with outcomes. Whole course treatment (surgery combined with adjuvant chemotherapy) significantly increased the value of ALB, but decreased the value of NLR, whereas it had no effect on the values of LDH, CRP or PLR. Post-/pre-treatment LDH and PLR were associated with outcomes. Post-/pre-treatment ALB, GLB, CRP and NLR were not associated with outcomes. Multivariate analysis revealed that a low pre-treatment ALB level and increased post-/pre-treatment PLR were independent risk factors affecting OS. The receiver operating characteristic curve analysis demonstrated that an ALB value of 47.850 g/l was considered to be the optimal cut-off value for prognosis; the sensitivity was 28.8% and specificity was 95.9%. It was suggested that the pre-treatment ALB and post-/pre-treatment PLR may be potential prognostic factors in resectable lung cancer.</description><subject>Adjuvant chemotherapy</subject><subject>Age</subject><subject>Albumin</subject><subject>Blood</subject><subject>Blood platelets</subject><subject>C-reactive protein</subject><subject>Cancer metastasis</subject><subject>Cancer patients</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Cellular proteins</subject><subject>Chemotherapy</subject><subject>Committees</subject><subject>Dehydrogenases</subject><subject>Development and progression</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Immune response</subject><subject>Inflammation</subject><subject>Lung cancer</subject><subject>Lymphocytes</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Metastasis</subject><subject>Mortality</subject><subject>Neutrophils</subject><subject>Oncology</subject><subject>Proteins</subject><subject>Risk factors</subject><subject>Surgery</subject><subject>Tumors</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptks9vFCEUxydGY5vam2cziYnx0F1hZvgxF5Om0WrSRA96Jm-YN7s0DKzAtNn_Xkjr2jXCgQd83hf48qrqNSXrVvbNB2_XDaFy3Usmn1WnVPTNihLZPD_EojupzmO8JbkxTqXkL6uTlnDBmp6cVvP34DfOx2R0jXdgF0jGu9pP9S5H6FKs703a1gEj6gSDxdoublNrcBpDvUSTJ3EfE85ZwbjJwjxD8mFfUnbeRcxKAWZMGOKr6sUENuL543hW_fz86cfVl9XNt-uvV5c3K80oSaueAsNeA4zdAHoaUOfbjnSAnkyoySDFyDllZJSac90NYhyY7nqhKW-BDKQ9qz4-6O6WYcZR53cEsGoXzAxhrzwYdbzjzFZt_J3ibUelKALvHwWC_7VgTGo2UaO14NAvUTXZ3Y4yQduMvv0HvfVLcPl5hepo1xIm_1IbsKiyTz6fq4uoumSiaynLUpla_4fKfSz2eoeTyetHCe-eJGwRbNpGb5fyifEYvHgAdfAxBpwOZlCiSikpb1UpJVVKKeNvnhp4gP8UTvsbt4HF5w</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Zhu, Jie</creator><creator>Lian, Lian</creator><creator>Qin, Hualong</creator><creator>Wang, Wen-Jie</creator><creator>Ren, Rui</creator><creator>Xu, Meng-Dan</creator><creator>Chen, Kai</creator><creator>Duan, Weiming</creator><creator>Gong, Fei-Ran</creator><creator>Tao, Min</creator><creator>Zhi, Qiaoming</creator><creator>Wu, Meng-Yao</creator><creator>Li, Wei</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190201</creationdate><title>Prognostic evaluation of patients with resectable lung cancer using systemic inflammatory response parameters</title><author>Zhu, Jie ; Lian, Lian ; Qin, Hualong ; Wang, Wen-Jie ; Ren, Rui ; Xu, Meng-Dan ; Chen, Kai ; Duan, Weiming ; Gong, Fei-Ran ; Tao, Min ; Zhi, Qiaoming ; Wu, Meng-Yao ; Li, Wei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-91a5e9caad4bacfbec752d1ba90fec0b87d66150d8c66c4b7db5c497c163a0b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adjuvant chemotherapy</topic><topic>Age</topic><topic>Albumin</topic><topic>Blood</topic><topic>Blood platelets</topic><topic>C-reactive protein</topic><topic>Cancer metastasis</topic><topic>Cancer patients</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Cellular proteins</topic><topic>Chemotherapy</topic><topic>Committees</topic><topic>Dehydrogenases</topic><topic>Development and progression</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Immune response</topic><topic>Inflammation</topic><topic>Lung cancer</topic><topic>Lymphocytes</topic><topic>Medical prognosis</topic><topic>Medical research</topic><topic>Metastasis</topic><topic>Mortality</topic><topic>Neutrophils</topic><topic>Oncology</topic><topic>Proteins</topic><topic>Risk factors</topic><topic>Surgery</topic><topic>Tumors</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Jie</creatorcontrib><creatorcontrib>Lian, Lian</creatorcontrib><creatorcontrib>Qin, Hualong</creatorcontrib><creatorcontrib>Wang, Wen-Jie</creatorcontrib><creatorcontrib>Ren, Rui</creatorcontrib><creatorcontrib>Xu, Meng-Dan</creatorcontrib><creatorcontrib>Chen, Kai</creatorcontrib><creatorcontrib>Duan, Weiming</creatorcontrib><creatorcontrib>Gong, Fei-Ran</creatorcontrib><creatorcontrib>Tao, Min</creatorcontrib><creatorcontrib>Zhi, Qiaoming</creatorcontrib><creatorcontrib>Wu, Meng-Yao</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><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>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 Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Jie</au><au>Lian, Lian</au><au>Qin, Hualong</au><au>Wang, Wen-Jie</au><au>Ren, Rui</au><au>Xu, Meng-Dan</au><au>Chen, Kai</au><au>Duan, Weiming</au><au>Gong, Fei-Ran</au><au>Tao, Min</au><au>Zhi, Qiaoming</au><au>Wu, Meng-Yao</au><au>Li, Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic evaluation of patients with resectable lung cancer using systemic inflammatory response parameters</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>17</volume><issue>2</issue><spage>2244</spage><epage>2256</epage><pages>2244-2256</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>Lung cancer is one of the leading causes of cancer-associated mortality. C-reactive protein (CRP), albumin (ALB), globulin (GLB), lactate dehydrogenase (LDH), neutrophil-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) have been identified as general parameters for systemic inflammatory response (SIR). Furthermore, these parameters are also associated with tumor development and metastasis. The present study aimed to investigate the predictive values of these SIR parameters in patients with resectable lung cancer. In total, 101 patients with resectable lung cancer were recruited in the present study. The patients were divided into two groups according to the median value of pre-treatment CRP, ALB, GLB, LDH, NLR or PLR values. The post-/pre-treatment ratios were defined as the ratio of pre-treatment blood parameter values and the corresponding values obtained following therapy. A ratio of ≤1.1 indicated that the values were not increased, while a ratio of >1.1 suggested that the values were increased following treatment. Patients with lower pre-treatment ALB levels had poorer overall survival (OS) rates, whereas GLB, LDH, CRP, NLR or PLR levels were not associated with outcomes. Whole course treatment (surgery combined with adjuvant chemotherapy) significantly increased the value of ALB, but decreased the value of NLR, whereas it had no effect on the values of LDH, CRP or PLR. Post-/pre-treatment LDH and PLR were associated with outcomes. Post-/pre-treatment ALB, GLB, CRP and NLR were not associated with outcomes. Multivariate analysis revealed that a low pre-treatment ALB level and increased post-/pre-treatment PLR were independent risk factors affecting OS. The receiver operating characteristic curve analysis demonstrated that an ALB value of 47.850 g/l was considered to be the optimal cut-off value for prognosis; the sensitivity was 28.8% and specificity was 95.9%. It was suggested that the pre-treatment ALB and post-/pre-treatment PLR may be potential prognostic factors in resectable lung cancer.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>30675290</pmid><doi>10.3892/ol.2018.9858</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvant chemotherapy Age Albumin Blood Blood platelets C-reactive protein Cancer metastasis Cancer patients Cancer therapies Care and treatment Cellular proteins Chemotherapy Committees Dehydrogenases Development and progression Gene expression Genetic aspects Health aspects Immune response Inflammation Lung cancer Lymphocytes Medical prognosis Medical research Metastasis Mortality Neutrophils Oncology Proteins Risk factors Surgery Tumors |
title | Prognostic evaluation of patients with resectable lung cancer using systemic inflammatory response parameters |
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