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Significance of inflammatory indexes in atezolizumab monotherapy outcomes in previously treated non-small-cell lung cancer patients
Cancer immunotherapy, including atezolizumab monotherapy, is a promising alternative strategy for patients with advanced non-small-cell lung cancer (NSCLC). Several inflammatory indices have been reported as potential biomarkers regarding the effectiveness of various treatments. This study aimed to...
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Published in: | Scientific reports 2020-10, Vol.10 (1), p.17495-17495, Article 17495 |
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creator | Katayama, Yuki Yamada, Tadaaki Chihara, Yusuke Tanaka, Satomi Tanimura, Keiko Okura, Naoko Hirose, Kazuki Uda, Sayaka Shiotsu, Shinsuke Hirai, Soichi Hiranuma, Osamu Harada, Taishi Shimamoto, Takayuki Iwasaku, Masahiro Kaneko, Yoshiko Uchino, Junji Takeda, Takayuki Takayama, Koichi |
description | Cancer immunotherapy, including atezolizumab monotherapy, is a promising alternative strategy for patients with advanced non-small-cell lung cancer (NSCLC). Several inflammatory indices have been reported as potential biomarkers regarding the effectiveness of various treatments. This study aimed to analyze the efficacy of atezolizumab monotherapy using baseline inflammatory markers in NSCLC patients. We retrospectively enrolled 81 NSCLC patients who received atezolizumab monotherapy at six different medical institutions in Japan. The Cox proportional hazards model was used to assess the impact of the clinical variables, including inflammatory indexes, on clinical outcomes. Median progression-free survival (PFS) and overall survival (OS) were 60 days and 252 days, respectively. The objective response rate was 7.4%, and the disease control rate was 54.3%. Patients with high neutrophil to lymphocyte ratio (NLR), low lymphocyte to monocyte ratio (LMR), and/or high platelet to lymphocyte ratio (PLR), at baseline, demonstrated substantially shorter PFS and OS compared to those with a low NLR, high LMR, and/or low PLR. The multivariate analysis demonstrated that a high baseline NLR was substantially associated with short PFS and short OS. Our retrospective observations suggest that inflammatory indices may be a potential negative prognostic factor of atezolizumab monotherapy outcomes in NSCLC patients. |
doi_str_mv | 10.1038/s41598-020-74573-0 |
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Several inflammatory indices have been reported as potential biomarkers regarding the effectiveness of various treatments. This study aimed to analyze the efficacy of atezolizumab monotherapy using baseline inflammatory markers in NSCLC patients. We retrospectively enrolled 81 NSCLC patients who received atezolizumab monotherapy at six different medical institutions in Japan. The Cox proportional hazards model was used to assess the impact of the clinical variables, including inflammatory indexes, on clinical outcomes. Median progression-free survival (PFS) and overall survival (OS) were 60 days and 252 days, respectively. The objective response rate was 7.4%, and the disease control rate was 54.3%. Patients with high neutrophil to lymphocyte ratio (NLR), low lymphocyte to monocyte ratio (LMR), and/or high platelet to lymphocyte ratio (PLR), at baseline, demonstrated substantially shorter PFS and OS compared to those with a low NLR, high LMR, and/or low PLR. The multivariate analysis demonstrated that a high baseline NLR was substantially associated with short PFS and short OS. Our retrospective observations suggest that inflammatory indices may be a potential negative prognostic factor of atezolizumab monotherapy outcomes in NSCLC patients.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-74573-0</identifier><identifier>PMID: 33060826</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/250 ; 631/67 ; 692/4028 ; 692/53 ; Adult ; Aged ; Aged, 80 and over ; Antibodies, Monoclonal, Humanized - therapeutic use ; Antineoplastic Agents - therapeutic use ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Disease-Free Survival ; Female ; Humanities and Social Sciences ; Humans ; Inflammation ; Japan ; Kaplan-Meier Estimate ; Lung Neoplasms - drug therapy ; Lymphocytes - cytology ; Male ; Middle Aged ; Monocytes - cytology ; multidisciplinary ; Multivariate Analysis ; Neutrophils - cytology ; Prognosis ; Proportional Hazards Models ; Retrospective Studies ; Science ; Science (multidisciplinary) ; Treatment Outcome</subject><ispartof>Scientific reports, 2020-10, Vol.10 (1), p.17495-17495, Article 17495</ispartof><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-3bb84937feaeccbc0b729d3fa3f185cfd2b0567f88cf28e7905fb5d6812f3a483</citedby><cites>FETCH-LOGICAL-c446t-3bb84937feaeccbc0b729d3fa3f185cfd2b0567f88cf28e7905fb5d6812f3a483</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/PMC7566597/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566597/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33060826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katayama, Yuki</creatorcontrib><creatorcontrib>Yamada, Tadaaki</creatorcontrib><creatorcontrib>Chihara, Yusuke</creatorcontrib><creatorcontrib>Tanaka, Satomi</creatorcontrib><creatorcontrib>Tanimura, Keiko</creatorcontrib><creatorcontrib>Okura, Naoko</creatorcontrib><creatorcontrib>Hirose, Kazuki</creatorcontrib><creatorcontrib>Uda, Sayaka</creatorcontrib><creatorcontrib>Shiotsu, Shinsuke</creatorcontrib><creatorcontrib>Hirai, Soichi</creatorcontrib><creatorcontrib>Hiranuma, Osamu</creatorcontrib><creatorcontrib>Harada, Taishi</creatorcontrib><creatorcontrib>Shimamoto, Takayuki</creatorcontrib><creatorcontrib>Iwasaku, Masahiro</creatorcontrib><creatorcontrib>Kaneko, Yoshiko</creatorcontrib><creatorcontrib>Uchino, Junji</creatorcontrib><creatorcontrib>Takeda, Takayuki</creatorcontrib><creatorcontrib>Takayama, Koichi</creatorcontrib><title>Significance of inflammatory indexes in atezolizumab monotherapy outcomes in previously treated non-small-cell lung cancer patients</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Cancer immunotherapy, including atezolizumab monotherapy, is a promising alternative strategy for patients with advanced non-small-cell lung cancer (NSCLC). Several inflammatory indices have been reported as potential biomarkers regarding the effectiveness of various treatments. This study aimed to analyze the efficacy of atezolizumab monotherapy using baseline inflammatory markers in NSCLC patients. We retrospectively enrolled 81 NSCLC patients who received atezolizumab monotherapy at six different medical institutions in Japan. The Cox proportional hazards model was used to assess the impact of the clinical variables, including inflammatory indexes, on clinical outcomes. Median progression-free survival (PFS) and overall survival (OS) were 60 days and 252 days, respectively. The objective response rate was 7.4%, and the disease control rate was 54.3%. Patients with high neutrophil to lymphocyte ratio (NLR), low lymphocyte to monocyte ratio (LMR), and/or high platelet to lymphocyte ratio (PLR), at baseline, demonstrated substantially shorter PFS and OS compared to those with a low NLR, high LMR, and/or low PLR. 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Several inflammatory indices have been reported as potential biomarkers regarding the effectiveness of various treatments. This study aimed to analyze the efficacy of atezolizumab monotherapy using baseline inflammatory markers in NSCLC patients. We retrospectively enrolled 81 NSCLC patients who received atezolizumab monotherapy at six different medical institutions in Japan. The Cox proportional hazards model was used to assess the impact of the clinical variables, including inflammatory indexes, on clinical outcomes. Median progression-free survival (PFS) and overall survival (OS) were 60 days and 252 days, respectively. The objective response rate was 7.4%, and the disease control rate was 54.3%. Patients with high neutrophil to lymphocyte ratio (NLR), low lymphocyte to monocyte ratio (LMR), and/or high platelet to lymphocyte ratio (PLR), at baseline, demonstrated substantially shorter PFS and OS compared to those with a low NLR, high LMR, and/or low PLR. The multivariate analysis demonstrated that a high baseline NLR was substantially associated with short PFS and short OS. Our retrospective observations suggest that inflammatory indices may be a potential negative prognostic factor of atezolizumab monotherapy outcomes in NSCLC patients.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33060826</pmid><doi>10.1038/s41598-020-74573-0</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/250 631/67 692/4028 692/53 Adult Aged Aged, 80 and over Antibodies, Monoclonal, Humanized - therapeutic use Antineoplastic Agents - therapeutic use Carcinoma, Non-Small-Cell Lung - drug therapy Disease-Free Survival Female Humanities and Social Sciences Humans Inflammation Japan Kaplan-Meier Estimate Lung Neoplasms - drug therapy Lymphocytes - cytology Male Middle Aged Monocytes - cytology multidisciplinary Multivariate Analysis Neutrophils - cytology Prognosis Proportional Hazards Models Retrospective Studies Science Science (multidisciplinary) Treatment Outcome |
title | Significance of inflammatory indexes in atezolizumab monotherapy outcomes in previously treated non-small-cell lung cancer patients |
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