Systemic inflammation scores correlate with survival prognosis in patients with newly diagnosed brain metastases

Background Systemic inflammation measured by the neutrophil-to-lymphocyte ratio (NLR), leucocyte-to-lymphocyte ratio (LLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR) and CRP/albumin ratio (CRP/Alb) was shown to impact the survival prognosis in patients with extracranial...

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Veröffentlicht in:British journal of cancer 2021-03, Vol.124 (7), p.1294-1300
Hauptverfasser: Starzer, Angelika M., Steindl, Ariane, Mair, Maximilian J., Deischinger, Carola, Simonovska, Anika, Widhalm, Georg, Gatterbauer, Brigitte, Dieckmann, Karin, Heller, Gerwin, Preusser, Matthias, Berghoff, Anna S.
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container_end_page 1300
container_issue 7
container_start_page 1294
container_title British journal of cancer
container_volume 124
creator Starzer, Angelika M.
Steindl, Ariane
Mair, Maximilian J.
Deischinger, Carola
Simonovska, Anika
Widhalm, Georg
Gatterbauer, Brigitte
Dieckmann, Karin
Heller, Gerwin
Preusser, Matthias
Berghoff, Anna S.
description Background Systemic inflammation measured by the neutrophil-to-lymphocyte ratio (NLR), leucocyte-to-lymphocyte ratio (LLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR) and CRP/albumin ratio (CRP/Alb) was shown to impact the survival prognosis in patients with extracranial solid cancer. Methods One thousand two hundred and fifty patients with newly diagnosed brain metastases (BM) were identified from the Vienna Brain Metastasis Registry. Results PLR and CRP/Alb were higher in patients with progressive extracranial disease and lower in patients with no evidence of extracranial disease. Lower NLR (cut-off = 5.07; 9.3 vs. 5.0 months), LLR (cut-off = 5.76; 10.0 vs. 5.3 months), PLR (cut-off = 335; 8.0 vs. 3.8 months), MLR (cut-off = 0.53; 6.0 vs. 3.5 months) and CRP/Alb (cut-off = 2.93; 8.5 vs. 3.7 months; p adj  
doi_str_mv 10.1038/s41416-020-01254-0
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Methods One thousand two hundred and fifty patients with newly diagnosed brain metastases (BM) were identified from the Vienna Brain Metastasis Registry. Results PLR and CRP/Alb were higher in patients with progressive extracranial disease and lower in patients with no evidence of extracranial disease. Lower NLR (cut-off = 5.07; 9.3 vs. 5.0 months), LLR (cut-off = 5.76; 10.0 vs. 5.3 months), PLR (cut-off = 335; 8.0 vs. 3.8 months), MLR (cut-off = 0.53; 6.0 vs. 3.5 months) and CRP/Alb (cut-off = 2.93; 8.5 vs. 3.7 months; p adj  &lt; 0.05) were associated with longer overall survival (OS). In multivariate analysis with graded prognostic assessment (hazard ratio (HR) 1.45; 95% confidence interval (CI): 1.32–1.59; p adj  = 1.62e − 13 ) , NLR (HR 1.55; 95% CI: 1.38–1.75; p adj  = 1.92e − 11), LLR (HR 1.57; 95% CI: 1.39–1.77; p adj  = 1.96e − 11 ) , PLR (HR 1.60; 95% CI: 1.39–1.85; p adj  = 2.87955e − 9), MLR (HR 1.41; 95% CI: 1.14–1.75; p adj  = 0.027) and CRP/Alb (HR 1.83; 95% CI: 1.54–2.18; p adj  = 2.73e − 10) remained independent factors associated with OS at BM diagnosis. Conclusions Systemic inflammation, measured by NLR, LLR, PLR, MLR and CRP/Alb, was associated with OS in patients with BM. Further exploration of immune modulating therapies is warranted in the setting of BM.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/s41416-020-01254-0</identifier><identifier>PMID: 33473170</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/308/409 ; 692/4028/67/1922 ; 692/53/2422 ; Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor - analysis ; Biomedical and Life Sciences ; Biomedicine ; Blood Platelets - pathology ; Brain cancer ; Brain Neoplasms - mortality ; Brain Neoplasms - secondary ; Brain Neoplasms - therapy ; Cancer Research ; Combined Modality Therapy ; Drug Resistance ; Epidemiology ; Female ; Follow-Up Studies ; Humans ; Inflammation ; Inflammation Mediators - analysis ; Leukocytes (neutrophilic) ; Lymphocytes ; Lymphocytes - pathology ; Medical prognosis ; Metastases ; Metastasis ; Middle Aged ; Molecular Medicine ; Monocytes ; Multivariate analysis ; Neoplasms - mortality ; Neoplasms - pathology ; Neoplasms - therapy ; Neutrophils - pathology ; Oncology ; Prognosis ; Retrospective Studies ; Survival Rate ; Young Adult</subject><ispartof>British journal of cancer, 2021-03, Vol.124 (7), p.1294-1300</ispartof><rights>The Author(s), under exclusive licence to The Author(s), under exclusive licence to Cancer Research UK 2021</rights><rights>The Author(s), under exclusive licence to The Author(s), under exclusive licence to Cancer Research UK 2021. 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-c474t-6186d6e1ac087e08c9192a48f0211d4d725b23375c380e5d9ebe29594f2251a73</citedby><cites>FETCH-LOGICAL-c474t-6186d6e1ac087e08c9192a48f0211d4d725b23375c380e5d9ebe29594f2251a73</cites><orcidid>0000-0002-6537-3874 ; 0000-0001-9379-6797 ; 0000-0001-8742-5631</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/PMC8007827/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007827/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33473170$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Starzer, Angelika M.</creatorcontrib><creatorcontrib>Steindl, Ariane</creatorcontrib><creatorcontrib>Mair, Maximilian J.</creatorcontrib><creatorcontrib>Deischinger, Carola</creatorcontrib><creatorcontrib>Simonovska, Anika</creatorcontrib><creatorcontrib>Widhalm, Georg</creatorcontrib><creatorcontrib>Gatterbauer, Brigitte</creatorcontrib><creatorcontrib>Dieckmann, Karin</creatorcontrib><creatorcontrib>Heller, Gerwin</creatorcontrib><creatorcontrib>Preusser, Matthias</creatorcontrib><creatorcontrib>Berghoff, Anna S.</creatorcontrib><title>Systemic inflammation scores correlate with survival prognosis in patients with newly diagnosed brain metastases</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Background Systemic inflammation measured by the neutrophil-to-lymphocyte ratio (NLR), leucocyte-to-lymphocyte ratio (LLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR) and CRP/albumin ratio (CRP/Alb) was shown to impact the survival prognosis in patients with extracranial solid cancer. Methods One thousand two hundred and fifty patients with newly diagnosed brain metastases (BM) were identified from the Vienna Brain Metastasis Registry. Results PLR and CRP/Alb were higher in patients with progressive extracranial disease and lower in patients with no evidence of extracranial disease. Lower NLR (cut-off = 5.07; 9.3 vs. 5.0 months), LLR (cut-off = 5.76; 10.0 vs. 5.3 months), PLR (cut-off = 335; 8.0 vs. 3.8 months), MLR (cut-off = 0.53; 6.0 vs. 3.5 months) and CRP/Alb (cut-off = 2.93; 8.5 vs. 3.7 months; p adj  &lt; 0.05) were associated with longer overall survival (OS). In multivariate analysis with graded prognostic assessment (hazard ratio (HR) 1.45; 95% confidence interval (CI): 1.32–1.59; p adj  = 1.62e − 13 ) , NLR (HR 1.55; 95% CI: 1.38–1.75; p adj  = 1.92e − 11), LLR (HR 1.57; 95% CI: 1.39–1.77; p adj  = 1.96e − 11 ) , PLR (HR 1.60; 95% CI: 1.39–1.85; p adj  = 2.87955e − 9), MLR (HR 1.41; 95% CI: 1.14–1.75; p adj  = 0.027) and CRP/Alb (HR 1.83; 95% CI: 1.54–2.18; p adj  = 2.73e − 10) remained independent factors associated with OS at BM diagnosis. Conclusions Systemic inflammation, measured by NLR, LLR, PLR, MLR and CRP/Alb, was associated with OS in patients with BM. Further exploration of immune modulating therapies is warranted in the setting of BM.</description><subject>692/308/409</subject><subject>692/4028/67/1922</subject><subject>692/53/2422</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood Platelets - pathology</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - mortality</subject><subject>Brain Neoplasms - secondary</subject><subject>Brain Neoplasms - therapy</subject><subject>Cancer Research</subject><subject>Combined Modality Therapy</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Inflammation Mediators - analysis</subject><subject>Leukocytes (neutrophilic)</subject><subject>Lymphocytes</subject><subject>Lymphocytes - pathology</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Monocytes</subject><subject>Multivariate analysis</subject><subject>Neoplasms - mortality</subject><subject>Neoplasms - pathology</subject><subject>Neoplasms - therapy</subject><subject>Neutrophils - pathology</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Survival Rate</subject><subject>Young Adult</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kUtv1TAQhS1ERS-FP8ACRWLDJnT8SJxskFBVHlKlLoC15etMbl0ldvAkt7r_Hl9SymNRybJlzXeOZ3wYe8XhHQfZnJPiitclCCiBi0qV8IRteCVFyRuhn7INAOgSWgGn7DnRbb620Ohn7FRKpSXXsGHT1wPNOHpX-NAPdhzt7GMoyMWEVOQ94WBnLO78fFPQkvZ-b4diSnEXInnKqmLKEgwzrUzAu-FQdN4eAeyKbbKZGXG2lBfSC3bS24Hw5f15xr5_vPx28bm8uv705eLDVemUVnNZ86buauTW5Y4RGtfyVljV9CA471SnRbUVUurKyQaw6lrcomirVvVCVNxqecber77Tsh2xc7nDZAczJT_adDDRevNvJfgbs4t70-RPy9-XDd7eG6T4Y0GazejJ4TDYgHEhI5RutVK15Bl98x96G5cU8nhGVFDrHIE8GoqVcikSJewfmuFgjoGaNVCTAzW_AjWQRa__HuNB8jvBDMgVoFwKO0x_3n7E9idfbK3-</recordid><startdate>20210330</startdate><enddate>20210330</enddate><creator>Starzer, Angelika M.</creator><creator>Steindl, Ariane</creator><creator>Mair, Maximilian J.</creator><creator>Deischinger, Carola</creator><creator>Simonovska, Anika</creator><creator>Widhalm, Georg</creator><creator>Gatterbauer, Brigitte</creator><creator>Dieckmann, Karin</creator><creator>Heller, Gerwin</creator><creator>Preusser, Matthias</creator><creator>Berghoff, Anna S.</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>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</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>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6537-3874</orcidid><orcidid>https://orcid.org/0000-0001-9379-6797</orcidid><orcidid>https://orcid.org/0000-0001-8742-5631</orcidid></search><sort><creationdate>20210330</creationdate><title>Systemic inflammation scores correlate with survival prognosis in patients with newly diagnosed brain metastases</title><author>Starzer, Angelika M. ; Steindl, Ariane ; Mair, Maximilian J. ; Deischinger, Carola ; Simonovska, Anika ; Widhalm, Georg ; Gatterbauer, Brigitte ; Dieckmann, Karin ; Heller, Gerwin ; Preusser, Matthias ; Berghoff, Anna S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-6186d6e1ac087e08c9192a48f0211d4d725b23375c380e5d9ebe29594f2251a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>692/308/409</topic><topic>692/4028/67/1922</topic><topic>692/53/2422</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blood Platelets - pathology</topic><topic>Brain cancer</topic><topic>Brain Neoplasms - mortality</topic><topic>Brain Neoplasms - secondary</topic><topic>Brain Neoplasms - therapy</topic><topic>Cancer Research</topic><topic>Combined Modality Therapy</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Inflammation Mediators - analysis</topic><topic>Leukocytes (neutrophilic)</topic><topic>Lymphocytes</topic><topic>Lymphocytes - pathology</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Molecular Medicine</topic><topic>Monocytes</topic><topic>Multivariate analysis</topic><topic>Neoplasms - mortality</topic><topic>Neoplasms - pathology</topic><topic>Neoplasms - therapy</topic><topic>Neutrophils - pathology</topic><topic>Oncology</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Survival Rate</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Starzer, Angelika M.</creatorcontrib><creatorcontrib>Steindl, Ariane</creatorcontrib><creatorcontrib>Mair, Maximilian J.</creatorcontrib><creatorcontrib>Deischinger, Carola</creatorcontrib><creatorcontrib>Simonovska, Anika</creatorcontrib><creatorcontrib>Widhalm, Georg</creatorcontrib><creatorcontrib>Gatterbauer, Brigitte</creatorcontrib><creatorcontrib>Dieckmann, Karin</creatorcontrib><creatorcontrib>Heller, Gerwin</creatorcontrib><creatorcontrib>Preusser, Matthias</creatorcontrib><creatorcontrib>Berghoff, Anna S.</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>Nursing &amp; 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Methods One thousand two hundred and fifty patients with newly diagnosed brain metastases (BM) were identified from the Vienna Brain Metastasis Registry. Results PLR and CRP/Alb were higher in patients with progressive extracranial disease and lower in patients with no evidence of extracranial disease. Lower NLR (cut-off = 5.07; 9.3 vs. 5.0 months), LLR (cut-off = 5.76; 10.0 vs. 5.3 months), PLR (cut-off = 335; 8.0 vs. 3.8 months), MLR (cut-off = 0.53; 6.0 vs. 3.5 months) and CRP/Alb (cut-off = 2.93; 8.5 vs. 3.7 months; p adj  &lt; 0.05) were associated with longer overall survival (OS). In multivariate analysis with graded prognostic assessment (hazard ratio (HR) 1.45; 95% confidence interval (CI): 1.32–1.59; p adj  = 1.62e − 13 ) , NLR (HR 1.55; 95% CI: 1.38–1.75; p adj  = 1.92e − 11), LLR (HR 1.57; 95% CI: 1.39–1.77; p adj  = 1.96e − 11 ) , PLR (HR 1.60; 95% CI: 1.39–1.85; p adj  = 2.87955e − 9), MLR (HR 1.41; 95% CI: 1.14–1.75; p adj  = 0.027) and CRP/Alb (HR 1.83; 95% CI: 1.54–2.18; p adj  = 2.73e − 10) remained independent factors associated with OS at BM diagnosis. Conclusions Systemic inflammation, measured by NLR, LLR, PLR, MLR and CRP/Alb, was associated with OS in patients with BM. Further exploration of immune modulating therapies is warranted in the setting of BM.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33473170</pmid><doi>10.1038/s41416-020-01254-0</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6537-3874</orcidid><orcidid>https://orcid.org/0000-0001-9379-6797</orcidid><orcidid>https://orcid.org/0000-0001-8742-5631</orcidid><oa>free_for_read</oa></addata></record>
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subjects 692/308/409
692/4028/67/1922
692/53/2422
Adult
Aged
Aged, 80 and over
Biomarkers, Tumor - analysis
Biomedical and Life Sciences
Biomedicine
Blood Platelets - pathology
Brain cancer
Brain Neoplasms - mortality
Brain Neoplasms - secondary
Brain Neoplasms - therapy
Cancer Research
Combined Modality Therapy
Drug Resistance
Epidemiology
Female
Follow-Up Studies
Humans
Inflammation
Inflammation Mediators - analysis
Leukocytes (neutrophilic)
Lymphocytes
Lymphocytes - pathology
Medical prognosis
Metastases
Metastasis
Middle Aged
Molecular Medicine
Monocytes
Multivariate analysis
Neoplasms - mortality
Neoplasms - pathology
Neoplasms - therapy
Neutrophils - pathology
Oncology
Prognosis
Retrospective Studies
Survival Rate
Young Adult
title Systemic inflammation scores correlate with survival prognosis in patients with newly diagnosed brain metastases
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