Epidemiologic and molecular prognostic review of glioblastoma
Glioblastoma multiforme (GBM) is the most common and aggressive primary central nervous system malignancy with a median survival of 15 months. The average incidence rate of GBM is 3.19/100,000 population, and the median age of diagnosis is 64 years. Incidence is higher in men and individuals of whit...
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Veröffentlicht in: | Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2014-10, Vol.23 (10), p.1985-1996 |
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container_end_page | 1996 |
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container_issue | 10 |
container_start_page | 1985 |
container_title | Cancer epidemiology, biomarkers & prevention |
container_volume | 23 |
creator | Thakkar, Jigisha P Dolecek, Therese A Horbinski, Craig Ostrom, Quinn T Lightner, Donita D Barnholtz-Sloan, Jill S Villano, John L |
description | Glioblastoma multiforme (GBM) is the most common and aggressive primary central nervous system malignancy with a median survival of 15 months. The average incidence rate of GBM is 3.19/100,000 population, and the median age of diagnosis is 64 years. Incidence is higher in men and individuals of white race and non-Hispanic ethnicity. Many genetic and environmental factors have been studied in GBM, but the majority are sporadic, and no risk factor accounting for a large proportion of GBMs has been identified. However, several favorable clinical prognostic factors are identified, including younger age at diagnosis, cerebellar location, high performance status, and maximal tumor resection. GBMs comprise of primary and secondary subtypes, which evolve through different genetic pathways, affect patients at different ages, and have differences in outcomes. We report the current epidemiology of GBM with new data from the Central Brain Tumor Registry of the United States 2006 to 2010 as well as demonstrate and discuss trends in incidence and survival. We also provide a concise review on molecular markers in GBM that have helped distinguish biologically similar subtypes of GBM and have prognostic and predictive value. |
doi_str_mv | 10.1158/1055-9965.EPI-14-0275 |
format | Article |
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The average incidence rate of GBM is 3.19/100,000 population, and the median age of diagnosis is 64 years. Incidence is higher in men and individuals of white race and non-Hispanic ethnicity. Many genetic and environmental factors have been studied in GBM, but the majority are sporadic, and no risk factor accounting for a large proportion of GBMs has been identified. However, several favorable clinical prognostic factors are identified, including younger age at diagnosis, cerebellar location, high performance status, and maximal tumor resection. GBMs comprise of primary and secondary subtypes, which evolve through different genetic pathways, affect patients at different ages, and have differences in outcomes. We report the current epidemiology of GBM with new data from the Central Brain Tumor Registry of the United States 2006 to 2010 as well as demonstrate and discuss trends in incidence and survival. 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We also provide a concise review on molecular markers in GBM that have helped distinguish biologically similar subtypes of GBM and have prognostic and predictive value.</description><subject>Age Distribution</subject><subject>Aged</subject><subject>Brain Neoplasms - epidemiology</subject><subject>Brain Neoplasms - genetics</subject><subject>Brain Neoplasms - pathology</subject><subject>Female</subject><subject>Glioblastoma - epidemiology</subject><subject>Glioblastoma - genetics</subject><subject>Glioblastoma - pathology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Sex Distribution</subject><issn>1055-9965</issn><issn>1538-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkNFKw0AQRRdRbK1-gpIfSN1JMsnmQUFK1EJBH_R52SQ7cSXJhk1a8e9NqC36NAN37h3uYewa-BIAxS1wRD9NY1xmr2sfIp8HCZ6wOWAo_CRBPB33w82MXfT9J-c8SRHP2SxAjmECMGd3WWdK3Rhb28oUnmpLr7G1Lra1cl7nbNXafhgFp3dGf3mWvKo2Nq9VP9hGXbIzUnWvr37ngr0_Zm-rZ3_z8rRePWz8AgUMPgkKgqhEiAJSRCSgFIAxhaTzPCROQTQqgpI45mmc5iUPqQDIcx6pknMKF-x-n9tt80aXhW4Hp2rZOdMo9y2tMvK_0poPWdmdjEAgH7suGO4DCmf73mk6eoHLiaecWMmJlRx5SojkxHP03fx9fHQdAIY_ng9z1w</recordid><startdate>20141001</startdate><enddate>20141001</enddate><creator>Thakkar, Jigisha P</creator><creator>Dolecek, Therese A</creator><creator>Horbinski, Craig</creator><creator>Ostrom, Quinn T</creator><creator>Lightner, Donita D</creator><creator>Barnholtz-Sloan, Jill S</creator><creator>Villano, John L</creator><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>5PM</scope></search><sort><creationdate>20141001</creationdate><title>Epidemiologic and molecular prognostic review of glioblastoma</title><author>Thakkar, Jigisha P ; Dolecek, Therese A ; Horbinski, Craig ; Ostrom, Quinn T ; Lightner, Donita D ; Barnholtz-Sloan, Jill S ; Villano, John L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c581t-f8f224d5142fafff81d8156f3febb3f0f2442f8f7660969bd03fc11bb04ad00f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Age Distribution</topic><topic>Aged</topic><topic>Brain Neoplasms - epidemiology</topic><topic>Brain Neoplasms - genetics</topic><topic>Brain Neoplasms - pathology</topic><topic>Female</topic><topic>Glioblastoma - epidemiology</topic><topic>Glioblastoma - genetics</topic><topic>Glioblastoma - pathology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Sex Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thakkar, Jigisha P</creatorcontrib><creatorcontrib>Dolecek, Therese A</creatorcontrib><creatorcontrib>Horbinski, Craig</creatorcontrib><creatorcontrib>Ostrom, Quinn T</creatorcontrib><creatorcontrib>Lightner, Donita D</creatorcontrib><creatorcontrib>Barnholtz-Sloan, Jill S</creatorcontrib><creatorcontrib>Villano, John L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thakkar, Jigisha P</au><au>Dolecek, Therese A</au><au>Horbinski, Craig</au><au>Ostrom, Quinn T</au><au>Lightner, Donita D</au><au>Barnholtz-Sloan, Jill S</au><au>Villano, John L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epidemiologic and molecular prognostic review of glioblastoma</atitle><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>23</volume><issue>10</issue><spage>1985</spage><epage>1996</epage><pages>1985-1996</pages><issn>1055-9965</issn><eissn>1538-7755</eissn><abstract>Glioblastoma multiforme (GBM) is the most common and aggressive primary central nervous system malignancy with a median survival of 15 months. 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We also provide a concise review on molecular markers in GBM that have helped distinguish biologically similar subtypes of GBM and have prognostic and predictive value.</abstract><cop>United States</cop><pmid>25053711</pmid><doi>10.1158/1055-9965.EPI-14-0275</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Distribution Aged Brain Neoplasms - epidemiology Brain Neoplasms - genetics Brain Neoplasms - pathology Female Glioblastoma - epidemiology Glioblastoma - genetics Glioblastoma - pathology Humans Incidence Male Middle Aged Prognosis Sex Distribution |
title | Epidemiologic and molecular prognostic review of glioblastoma |
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