Racial and socioeconomic disparities in glioblastoma outcomes: A single‐center, retrospective cohort study
Background Glioblastoma (GBM) is the most common malignant primary brain tumor. Emerging reports have suggested that racial and socioeconomic disparities influence the outcomes of patients with GBM. No studies to date have investigated these disparities controlling for isocitrate dehydrogenase (IDH)...
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Veröffentlicht in: | Cancer 2023-10, Vol.129 (19), p.3010-3022 |
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creator | Estevez‐Ordonez, Dagoberto Abdelrashid, Moaaz Coffee, Elizabeth Laskay, Nicholas M. B. Atchley, Travis J. Chkheidze, Rati Fiveash, John B. Markert, James M. Lobbous, Mina Maveal, Brandon M. Burt Nabors, Louis |
description | Background
Glioblastoma (GBM) is the most common malignant primary brain tumor. Emerging reports have suggested that racial and socioeconomic disparities influence the outcomes of patients with GBM. No studies to date have investigated these disparities controlling for isocitrate dehydrogenase (IDH) mutation and O‐6‐methylguanine‐DNA methyltransferase (MGMT) status.
Methods
Adult patients with GBM were retrospectively reviewed at a single institution from 2008 to 2019. Univariable and multivariable complete survival analyses were performed. A Cox proportional hazards model was used to assess the effect of race and socioeconomic status controlling for a priori selected variables with known relevance to survival.
Results
In total, 995 patients met inclusion criteria. Of these, 117 patients (11.7%) were African American (AA). The median overall survival for the entire cohort was 14.23 months. In the multivariable model, AA patients had better survival compared with White patients (hazard ratio [HR], 0.37; 95% confidence interval [CI], 0.2–0.69). The observed survival difference was significant in both a complete case analysis model and a multiple imputations model accounting for missing molecular data and controlling for treatment and socioeconomic status. AA patients with low income (HR, 2.17; 95% CI, 1.04–4.50), public insurance (HR, 2.25; 95% CI, 1.04–4.87), or no insurance (HR, 15.63; 95% CI, 2.72–89.67) had worse survival compared with White patients with low income, public insurance, or no insurance, respectively.
Conclusions
Significant racial and socioeconomic disparities were identified after controlling for treatment, GBM genetic profile, and other variables associated with survival. Overall, AA patients demonstrated better survival. These findings may suggest the possibility of a protective genetic advantage in AA patients.
Plain Language Summary
To best personalize treatment for and understand the causes of glioblastoma, racial and socioeconomic influences must be examined.
The authors report their experience at the O’Neal Comprehensive Cancer Center in the deep south.
In this report, contemporary molecular diagnostic data are included.
The authors conclude that there are significant racial and socioeconomic disparities that influence glioblastoma outcome and that African American patients do better.
Racial and socioeconomic factors influence glioblastoma outcomes in the Deep South. African American patients do better when controlling for other va |
doi_str_mv | 10.1002/cncr.34881 |
format | Article |
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Glioblastoma (GBM) is the most common malignant primary brain tumor. Emerging reports have suggested that racial and socioeconomic disparities influence the outcomes of patients with GBM. No studies to date have investigated these disparities controlling for isocitrate dehydrogenase (IDH) mutation and O‐6‐methylguanine‐DNA methyltransferase (MGMT) status.
Methods
Adult patients with GBM were retrospectively reviewed at a single institution from 2008 to 2019. Univariable and multivariable complete survival analyses were performed. A Cox proportional hazards model was used to assess the effect of race and socioeconomic status controlling for a priori selected variables with known relevance to survival.
Results
In total, 995 patients met inclusion criteria. Of these, 117 patients (11.7%) were African American (AA). The median overall survival for the entire cohort was 14.23 months. In the multivariable model, AA patients had better survival compared with White patients (hazard ratio [HR], 0.37; 95% confidence interval [CI], 0.2–0.69). The observed survival difference was significant in both a complete case analysis model and a multiple imputations model accounting for missing molecular data and controlling for treatment and socioeconomic status. AA patients with low income (HR, 2.17; 95% CI, 1.04–4.50), public insurance (HR, 2.25; 95% CI, 1.04–4.87), or no insurance (HR, 15.63; 95% CI, 2.72–89.67) had worse survival compared with White patients with low income, public insurance, or no insurance, respectively.
Conclusions
Significant racial and socioeconomic disparities were identified after controlling for treatment, GBM genetic profile, and other variables associated with survival. Overall, AA patients demonstrated better survival. These findings may suggest the possibility of a protective genetic advantage in AA patients.
Plain Language Summary
To best personalize treatment for and understand the causes of glioblastoma, racial and socioeconomic influences must be examined.
The authors report their experience at the O’Neal Comprehensive Cancer Center in the deep south.
In this report, contemporary molecular diagnostic data are included.
The authors conclude that there are significant racial and socioeconomic disparities that influence glioblastoma outcome and that African American patients do better.
Racial and socioeconomic factors influence glioblastoma outcomes in the Deep South. African American patients do better when controlling for other variables.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.34881</identifier><identifier>PMID: 37246417</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Brain cancer ; Brain Neoplasms - diagnosis ; Brain Neoplasms - genetics ; Brain Neoplasms - therapy ; Brain tumors ; Cohort analysis ; disparities ; DNA methyltransferase ; Glioblastoma ; Glioblastoma - diagnosis ; Glioblastoma - genetics ; Glioblastoma - therapy ; Hazard assessment ; Healthcare Disparities ; Humans ; Income ; Insurance ; Isocitrate dehydrogenase ; Low income groups ; Methylguanine ; O6-methylguanine-DNA methyltransferase ; Oncology ; race ; Retrospective Studies ; Socioeconomic Disparities in Health ; Socioeconomic factors ; socioeconomic status ; Socioeconomics ; Statistical models ; Survival ; Survival Analysis</subject><ispartof>Cancer, 2023-10, Vol.129 (19), p.3010-3022</ispartof><rights>2023 The Authors. published by Wiley Periodicals LLC on behalf of American Cancer Society.</rights><rights>2023 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc/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-c3931-478ba3d3b559147f1af49955167f20404502ff64d10a3aeacea42d4c13583bfc3</citedby><cites>FETCH-LOGICAL-c3931-478ba3d3b559147f1af49955167f20404502ff64d10a3aeacea42d4c13583bfc3</cites><orcidid>0000-0002-5679-0692 ; 0000-0001-5926-2230 ; 0000-0001-8615-0103</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.34881$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.34881$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37246417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Estevez‐Ordonez, Dagoberto</creatorcontrib><creatorcontrib>Abdelrashid, Moaaz</creatorcontrib><creatorcontrib>Coffee, Elizabeth</creatorcontrib><creatorcontrib>Laskay, Nicholas M. B.</creatorcontrib><creatorcontrib>Atchley, Travis J.</creatorcontrib><creatorcontrib>Chkheidze, Rati</creatorcontrib><creatorcontrib>Fiveash, John B.</creatorcontrib><creatorcontrib>Markert, James M.</creatorcontrib><creatorcontrib>Lobbous, Mina</creatorcontrib><creatorcontrib>Maveal, Brandon M.</creatorcontrib><creatorcontrib>Burt Nabors, Louis</creatorcontrib><title>Racial and socioeconomic disparities in glioblastoma outcomes: A single‐center, retrospective cohort study</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Background
Glioblastoma (GBM) is the most common malignant primary brain tumor. Emerging reports have suggested that racial and socioeconomic disparities influence the outcomes of patients with GBM. No studies to date have investigated these disparities controlling for isocitrate dehydrogenase (IDH) mutation and O‐6‐methylguanine‐DNA methyltransferase (MGMT) status.
Methods
Adult patients with GBM were retrospectively reviewed at a single institution from 2008 to 2019. Univariable and multivariable complete survival analyses were performed. A Cox proportional hazards model was used to assess the effect of race and socioeconomic status controlling for a priori selected variables with known relevance to survival.
Results
In total, 995 patients met inclusion criteria. Of these, 117 patients (11.7%) were African American (AA). The median overall survival for the entire cohort was 14.23 months. In the multivariable model, AA patients had better survival compared with White patients (hazard ratio [HR], 0.37; 95% confidence interval [CI], 0.2–0.69). The observed survival difference was significant in both a complete case analysis model and a multiple imputations model accounting for missing molecular data and controlling for treatment and socioeconomic status. AA patients with low income (HR, 2.17; 95% CI, 1.04–4.50), public insurance (HR, 2.25; 95% CI, 1.04–4.87), or no insurance (HR, 15.63; 95% CI, 2.72–89.67) had worse survival compared with White patients with low income, public insurance, or no insurance, respectively.
Conclusions
Significant racial and socioeconomic disparities were identified after controlling for treatment, GBM genetic profile, and other variables associated with survival. Overall, AA patients demonstrated better survival. These findings may suggest the possibility of a protective genetic advantage in AA patients.
Plain Language Summary
To best personalize treatment for and understand the causes of glioblastoma, racial and socioeconomic influences must be examined.
The authors report their experience at the O’Neal Comprehensive Cancer Center in the deep south.
In this report, contemporary molecular diagnostic data are included.
The authors conclude that there are significant racial and socioeconomic disparities that influence glioblastoma outcome and that African American patients do better.
Racial and socioeconomic factors influence glioblastoma outcomes in the Deep South. African American patients do better when controlling for other variables.</description><subject>Adult</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - diagnosis</subject><subject>Brain Neoplasms - genetics</subject><subject>Brain Neoplasms - therapy</subject><subject>Brain tumors</subject><subject>Cohort analysis</subject><subject>disparities</subject><subject>DNA methyltransferase</subject><subject>Glioblastoma</subject><subject>Glioblastoma - diagnosis</subject><subject>Glioblastoma - genetics</subject><subject>Glioblastoma - therapy</subject><subject>Hazard assessment</subject><subject>Healthcare Disparities</subject><subject>Humans</subject><subject>Income</subject><subject>Insurance</subject><subject>Isocitrate dehydrogenase</subject><subject>Low income groups</subject><subject>Methylguanine</subject><subject>O6-methylguanine-DNA methyltransferase</subject><subject>Oncology</subject><subject>race</subject><subject>Retrospective Studies</subject><subject>Socioeconomic Disparities in Health</subject><subject>Socioeconomic factors</subject><subject>socioeconomic status</subject><subject>Socioeconomics</subject><subject>Statistical models</subject><subject>Survival</subject><subject>Survival Analysis</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp90ctq3DAUBmBRUjrTNJs-QBBkE0Kd6upLdoNJLzAkMLSQnZHl40RBtiaS3DK7PkKfsU9STT3tIouuxIGPX0f6EXpLySUlhL3Xo_aXXJQlfYGWlFRFRqhgR2hJCCkzKfjdAr0O4TGNBZP8FVrwgolc0GKJ7EZpoyxWY4eD08aBdqMbjMadCVvlTTQQsBnxvTWutSpENyjspqjdAOEKr3Aw472FXz9-ahgj-HfYQ_QubEFH8w2wdg_ORxzi1O3eoJe9sgFODucx-vrh-kv9KVvffvxcr9aZ5hWnmSjKVvGOt1JWVBQ9Vb2oKilpXvSMCCIkYX2fi44SxRUoDUqwTmjKZcnbXvNjdD7nbr17miDEZjBBg7VqBDeFhpWMcJ7Tiid69ow-usmPabukZJWn-zlN6mJWOr0seOibrTeD8ruGkmbfQbPvoPnTQcKnh8ipHaD7R_9-egJ0Bt-Nhd1_opr6pt7Mob8BVTqTMw</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Estevez‐Ordonez, Dagoberto</creator><creator>Abdelrashid, Moaaz</creator><creator>Coffee, Elizabeth</creator><creator>Laskay, Nicholas M. B.</creator><creator>Atchley, Travis J.</creator><creator>Chkheidze, Rati</creator><creator>Fiveash, John B.</creator><creator>Markert, James M.</creator><creator>Lobbous, Mina</creator><creator>Maveal, Brandon M.</creator><creator>Burt Nabors, Louis</creator><general>Wiley Subscription Services, Inc</general><scope>24P</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>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5679-0692</orcidid><orcidid>https://orcid.org/0000-0001-5926-2230</orcidid><orcidid>https://orcid.org/0000-0001-8615-0103</orcidid></search><sort><creationdate>20231001</creationdate><title>Racial and socioeconomic disparities in glioblastoma outcomes: A single‐center, retrospective cohort study</title><author>Estevez‐Ordonez, Dagoberto ; Abdelrashid, Moaaz ; Coffee, Elizabeth ; Laskay, Nicholas M. B. ; Atchley, Travis J. ; Chkheidze, Rati ; Fiveash, John B. ; Markert, James M. ; Lobbous, Mina ; Maveal, Brandon M. ; Burt Nabors, Louis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3931-478ba3d3b559147f1af49955167f20404502ff64d10a3aeacea42d4c13583bfc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Brain cancer</topic><topic>Brain Neoplasms - diagnosis</topic><topic>Brain Neoplasms - genetics</topic><topic>Brain Neoplasms - therapy</topic><topic>Brain tumors</topic><topic>Cohort analysis</topic><topic>disparities</topic><topic>DNA methyltransferase</topic><topic>Glioblastoma</topic><topic>Glioblastoma - diagnosis</topic><topic>Glioblastoma - genetics</topic><topic>Glioblastoma - therapy</topic><topic>Hazard assessment</topic><topic>Healthcare Disparities</topic><topic>Humans</topic><topic>Income</topic><topic>Insurance</topic><topic>Isocitrate dehydrogenase</topic><topic>Low income groups</topic><topic>Methylguanine</topic><topic>O6-methylguanine-DNA methyltransferase</topic><topic>Oncology</topic><topic>race</topic><topic>Retrospective Studies</topic><topic>Socioeconomic Disparities in Health</topic><topic>Socioeconomic factors</topic><topic>socioeconomic status</topic><topic>Socioeconomics</topic><topic>Statistical models</topic><topic>Survival</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Estevez‐Ordonez, Dagoberto</creatorcontrib><creatorcontrib>Abdelrashid, Moaaz</creatorcontrib><creatorcontrib>Coffee, Elizabeth</creatorcontrib><creatorcontrib>Laskay, Nicholas M. B.</creatorcontrib><creatorcontrib>Atchley, Travis J.</creatorcontrib><creatorcontrib>Chkheidze, Rati</creatorcontrib><creatorcontrib>Fiveash, John B.</creatorcontrib><creatorcontrib>Markert, James M.</creatorcontrib><creatorcontrib>Lobbous, Mina</creatorcontrib><creatorcontrib>Maveal, Brandon M.</creatorcontrib><creatorcontrib>Burt Nabors, Louis</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Estevez‐Ordonez, Dagoberto</au><au>Abdelrashid, Moaaz</au><au>Coffee, Elizabeth</au><au>Laskay, Nicholas M. B.</au><au>Atchley, Travis J.</au><au>Chkheidze, Rati</au><au>Fiveash, John B.</au><au>Markert, James M.</au><au>Lobbous, Mina</au><au>Maveal, Brandon M.</au><au>Burt Nabors, Louis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Racial and socioeconomic disparities in glioblastoma outcomes: A single‐center, retrospective cohort study</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2023-10-01</date><risdate>2023</risdate><volume>129</volume><issue>19</issue><spage>3010</spage><epage>3022</epage><pages>3010-3022</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>Background
Glioblastoma (GBM) is the most common malignant primary brain tumor. Emerging reports have suggested that racial and socioeconomic disparities influence the outcomes of patients with GBM. No studies to date have investigated these disparities controlling for isocitrate dehydrogenase (IDH) mutation and O‐6‐methylguanine‐DNA methyltransferase (MGMT) status.
Methods
Adult patients with GBM were retrospectively reviewed at a single institution from 2008 to 2019. Univariable and multivariable complete survival analyses were performed. A Cox proportional hazards model was used to assess the effect of race and socioeconomic status controlling for a priori selected variables with known relevance to survival.
Results
In total, 995 patients met inclusion criteria. Of these, 117 patients (11.7%) were African American (AA). The median overall survival for the entire cohort was 14.23 months. In the multivariable model, AA patients had better survival compared with White patients (hazard ratio [HR], 0.37; 95% confidence interval [CI], 0.2–0.69). The observed survival difference was significant in both a complete case analysis model and a multiple imputations model accounting for missing molecular data and controlling for treatment and socioeconomic status. AA patients with low income (HR, 2.17; 95% CI, 1.04–4.50), public insurance (HR, 2.25; 95% CI, 1.04–4.87), or no insurance (HR, 15.63; 95% CI, 2.72–89.67) had worse survival compared with White patients with low income, public insurance, or no insurance, respectively.
Conclusions
Significant racial and socioeconomic disparities were identified after controlling for treatment, GBM genetic profile, and other variables associated with survival. Overall, AA patients demonstrated better survival. These findings may suggest the possibility of a protective genetic advantage in AA patients.
Plain Language Summary
To best personalize treatment for and understand the causes of glioblastoma, racial and socioeconomic influences must be examined.
The authors report their experience at the O’Neal Comprehensive Cancer Center in the deep south.
In this report, contemporary molecular diagnostic data are included.
The authors conclude that there are significant racial and socioeconomic disparities that influence glioblastoma outcome and that African American patients do better.
Racial and socioeconomic factors influence glioblastoma outcomes in the Deep South. African American patients do better when controlling for other variables.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37246417</pmid><doi>10.1002/cncr.34881</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-5679-0692</orcidid><orcidid>https://orcid.org/0000-0001-5926-2230</orcidid><orcidid>https://orcid.org/0000-0001-8615-0103</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Brain cancer Brain Neoplasms - diagnosis Brain Neoplasms - genetics Brain Neoplasms - therapy Brain tumors Cohort analysis disparities DNA methyltransferase Glioblastoma Glioblastoma - diagnosis Glioblastoma - genetics Glioblastoma - therapy Hazard assessment Healthcare Disparities Humans Income Insurance Isocitrate dehydrogenase Low income groups Methylguanine O6-methylguanine-DNA methyltransferase Oncology race Retrospective Studies Socioeconomic Disparities in Health Socioeconomic factors socioeconomic status Socioeconomics Statistical models Survival Survival Analysis |
title | Racial and socioeconomic disparities in glioblastoma outcomes: A single‐center, retrospective cohort study |
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