Incidence of high grade gliomas presenting as radiographically non-enhancing lesions: experience in 111 surgically treated non-enhancing gliomas with tissue diagnosis

Purpose Although non-enhancing lesions suspicious for glioma are usually assumed to be low grade glioma (LGG), some high grade glioma (HGG) do not enhance, which may lead to a delay in biopsy and/or resection, diagnosis, and treatment initiation. Thus, there is a clear need for a large-sample study...

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Veröffentlicht in:Journal of neuro-oncology 2020-05, Vol.147 (3), p.671-679
Hauptverfasser: Eichberg, Daniel G., Di, Long, Morell, Alexis A., Shah, Ashish H., Semonche, Alexa M., Chin, Christopher N., Bhatia, Rita G., Jamshidi, Aria M., Luther, Evan M., Komotar, Ricardo J., Ivan, Michael E.
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container_title Journal of neuro-oncology
container_volume 147
creator Eichberg, Daniel G.
Di, Long
Morell, Alexis A.
Shah, Ashish H.
Semonche, Alexa M.
Chin, Christopher N.
Bhatia, Rita G.
Jamshidi, Aria M.
Luther, Evan M.
Komotar, Ricardo J.
Ivan, Michael E.
description Purpose Although non-enhancing lesions suspicious for glioma are usually assumed to be low grade glioma (LGG), some high grade glioma (HGG) do not enhance, which may lead to a delay in biopsy and/or resection, diagnosis, and treatment initiation. Thus, there is a clear need for a large-sample study that quantifies the rate of malignant, non-enhancing gliomas. Methods We retrospectively reviewed our series of 561 consecutive surgically treated gliomas with tissue diagnosis, 111 of which were non-enhancing, to determine the prevalence of high-grade histology in radiographically presumed LGG. Relative expression of tumor markers were also reported for non-enhancing lesions to investigate genetic correlates. Results We identified 561 surgically treated gliomas with tissue diagnosis from August 2012 to July 2018 and found that 111 patients (19.8%) demonstrated non-enhancing lesions suspicious for glioma on preoperative MRI. Thirty-one (27.9%) of the non-enhancing lesions were classified as HGGs (WHO Grade III or IV). Non-enhancing lesions were four times more likely to be HGG in patients older than 60 years than patients younger than 35 years (41.2% vs. 11.4%, Pearson Chi 2 p 
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Thus, there is a clear need for a large-sample study that quantifies the rate of malignant, non-enhancing gliomas. Methods We retrospectively reviewed our series of 561 consecutive surgically treated gliomas with tissue diagnosis, 111 of which were non-enhancing, to determine the prevalence of high-grade histology in radiographically presumed LGG. Relative expression of tumor markers were also reported for non-enhancing lesions to investigate genetic correlates. Results We identified 561 surgically treated gliomas with tissue diagnosis from August 2012 to July 2018 and found that 111 patients (19.8%) demonstrated non-enhancing lesions suspicious for glioma on preoperative MRI. Thirty-one (27.9%) of the non-enhancing lesions were classified as HGGs (WHO Grade III or IV). Non-enhancing lesions were four times more likely to be HGG in patients older than 60 years than patients younger than 35 years (41.2% vs. 11.4%, Pearson Chi 2 p &lt; 0.001). Binomial logistic regression showed a significant inverse effect of age on the presence of IDH mutation in non-enhancing HGGs (p = 0.007). Conclusion A clinically significant proportion (27.9%) of non-enhancing lesions were found to be HGG on final pathologic diagnosis. Thus, in patients with good functional and health status, especially those older than 60 years, we recommend obtaining tissue diagnosis of all lesions suspected to be glioma, even those that are non-enhancing, to guide diagnosis as well as early initiation of chemotherapy and radiation therapy.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1007/s11060-020-03474-z</identifier><identifier>PMID: 32221785</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Biopsy ; Brain Neoplasms - diagnostic imaging ; Brain Neoplasms - epidemiology ; Brain Neoplasms - pathology ; Brain Neoplasms - surgery ; Chemotherapy ; Clinical Study ; Diagnosis ; Female ; Glioma ; Glioma - diagnostic imaging ; Glioma - epidemiology ; Glioma - pathology ; Glioma - surgery ; Humans ; Incidence ; Lesions ; Magnetic Resonance Imaging ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Neurology ; Oncology ; Radiation therapy ; Retrospective Studies ; Treatment Outcome ; Tumor markers ; Young Adult</subject><ispartof>Journal of neuro-oncology, 2020-05, Vol.147 (3), p.671-679</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-fb786107a69838b44f5521cdf3fed5a0a12c721bfb7d635e6689d9de010031e93</citedby><cites>FETCH-LOGICAL-c375t-fb786107a69838b44f5521cdf3fed5a0a12c721bfb7d635e6689d9de010031e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11060-020-03474-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11060-020-03474-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32221785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eichberg, Daniel G.</creatorcontrib><creatorcontrib>Di, Long</creatorcontrib><creatorcontrib>Morell, Alexis A.</creatorcontrib><creatorcontrib>Shah, Ashish H.</creatorcontrib><creatorcontrib>Semonche, Alexa M.</creatorcontrib><creatorcontrib>Chin, Christopher N.</creatorcontrib><creatorcontrib>Bhatia, Rita G.</creatorcontrib><creatorcontrib>Jamshidi, Aria M.</creatorcontrib><creatorcontrib>Luther, Evan M.</creatorcontrib><creatorcontrib>Komotar, Ricardo J.</creatorcontrib><creatorcontrib>Ivan, Michael E.</creatorcontrib><title>Incidence of high grade gliomas presenting as radiographically non-enhancing lesions: experience in 111 surgically treated non-enhancing gliomas with tissue diagnosis</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><addtitle>J Neurooncol</addtitle><description>Purpose Although non-enhancing lesions suspicious for glioma are usually assumed to be low grade glioma (LGG), some high grade glioma (HGG) do not enhance, which may lead to a delay in biopsy and/or resection, diagnosis, and treatment initiation. Thus, there is a clear need for a large-sample study that quantifies the rate of malignant, non-enhancing gliomas. Methods We retrospectively reviewed our series of 561 consecutive surgically treated gliomas with tissue diagnosis, 111 of which were non-enhancing, to determine the prevalence of high-grade histology in radiographically presumed LGG. Relative expression of tumor markers were also reported for non-enhancing lesions to investigate genetic correlates. Results We identified 561 surgically treated gliomas with tissue diagnosis from August 2012 to July 2018 and found that 111 patients (19.8%) demonstrated non-enhancing lesions suspicious for glioma on preoperative MRI. Thirty-one (27.9%) of the non-enhancing lesions were classified as HGGs (WHO Grade III or IV). Non-enhancing lesions were four times more likely to be HGG in patients older than 60 years than patients younger than 35 years (41.2% vs. 11.4%, Pearson Chi 2 p &lt; 0.001). Binomial logistic regression showed a significant inverse effect of age on the presence of IDH mutation in non-enhancing HGGs (p = 0.007). Conclusion A clinically significant proportion (27.9%) of non-enhancing lesions were found to be HGG on final pathologic diagnosis. Thus, in patients with good functional and health status, especially those older than 60 years, we recommend obtaining tissue diagnosis of all lesions suspected to be glioma, even those that are non-enhancing, to guide diagnosis as well as early initiation of chemotherapy and radiation therapy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biopsy</subject><subject>Brain Neoplasms - diagnostic imaging</subject><subject>Brain Neoplasms - epidemiology</subject><subject>Brain Neoplasms - pathology</subject><subject>Brain Neoplasms - surgery</subject><subject>Chemotherapy</subject><subject>Clinical Study</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Glioma</subject><subject>Glioma - diagnostic imaging</subject><subject>Glioma - epidemiology</subject><subject>Glioma - pathology</subject><subject>Glioma - surgery</subject><subject>Humans</subject><subject>Incidence</subject><subject>Lesions</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Oncology</subject><subject>Radiation therapy</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><subject>Tumor markers</subject><subject>Young Adult</subject><issn>0167-594X</issn><issn>1573-7373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kU9rFTEUxYNY7LP6BVxIwE03o_k7mXEnpdVCwU0FdyFvcmcmZV4y5s6g7Qfq5zT2vSp04SKEcH_nnEsOIW84e88ZMx-Qc1aziolypDKquntGNlwbWRlp5HOyYbw2lW7V92PyEvGGMaaM5C_IsRRCcNPoDbm_jF3wEDugqadjGEY6ZOeBDlNIO4d0zoAQlxAHWl5lFFIB5jF0bppuaUyxgji64lKICTCkiB8p_JohhwfbECnnnOKah4NmyeAW8E-0j4E_wzLSJSCuQH1wQ0wY8BU56t2E8Ppwn5BvF-fXZ1-qq6-fL88-XVWdNHqp-q1pas6Mq9tGNluleq0F73wve_DaMcdFZwTfFs7XUkNdN61vPbDyn5JDK0_I6d53zunHCrjYXcAOpslFSCtaIRslmFLGFPTdE_QmrTmW7axQzJRgoVWhxJ7qckLM0Ns5h53Lt5Yz-6dFu2_RlhbtQ4v2rojeHqzX7Q78X8ljbQWQewDLKA6Q_2X_x_Y3WTmrVg</recordid><startdate>20200501</startdate><enddate>20200501</enddate><creator>Eichberg, Daniel G.</creator><creator>Di, Long</creator><creator>Morell, Alexis A.</creator><creator>Shah, Ashish H.</creator><creator>Semonche, Alexa M.</creator><creator>Chin, Christopher N.</creator><creator>Bhatia, Rita G.</creator><creator>Jamshidi, Aria M.</creator><creator>Luther, Evan M.</creator><creator>Komotar, Ricardo J.</creator><creator>Ivan, Michael E.</creator><general>Springer US</general><general>Springer Nature B.V</general><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>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20200501</creationdate><title>Incidence of high grade gliomas presenting as radiographically non-enhancing lesions: experience in 111 surgically treated non-enhancing gliomas with tissue diagnosis</title><author>Eichberg, Daniel G. ; 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Thus, there is a clear need for a large-sample study that quantifies the rate of malignant, non-enhancing gliomas. Methods We retrospectively reviewed our series of 561 consecutive surgically treated gliomas with tissue diagnosis, 111 of which were non-enhancing, to determine the prevalence of high-grade histology in radiographically presumed LGG. Relative expression of tumor markers were also reported for non-enhancing lesions to investigate genetic correlates. Results We identified 561 surgically treated gliomas with tissue diagnosis from August 2012 to July 2018 and found that 111 patients (19.8%) demonstrated non-enhancing lesions suspicious for glioma on preoperative MRI. Thirty-one (27.9%) of the non-enhancing lesions were classified as HGGs (WHO Grade III or IV). Non-enhancing lesions were four times more likely to be HGG in patients older than 60 years than patients younger than 35 years (41.2% vs. 11.4%, Pearson Chi 2 p &lt; 0.001). Binomial logistic regression showed a significant inverse effect of age on the presence of IDH mutation in non-enhancing HGGs (p = 0.007). Conclusion A clinically significant proportion (27.9%) of non-enhancing lesions were found to be HGG on final pathologic diagnosis. Thus, in patients with good functional and health status, especially those older than 60 years, we recommend obtaining tissue diagnosis of all lesions suspected to be glioma, even those that are non-enhancing, to guide diagnosis as well as early initiation of chemotherapy and radiation therapy.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32221785</pmid><doi>10.1007/s11060-020-03474-z</doi><tpages>9</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Biopsy
Brain Neoplasms - diagnostic imaging
Brain Neoplasms - epidemiology
Brain Neoplasms - pathology
Brain Neoplasms - surgery
Chemotherapy
Clinical Study
Diagnosis
Female
Glioma
Glioma - diagnostic imaging
Glioma - epidemiology
Glioma - pathology
Glioma - surgery
Humans
Incidence
Lesions
Magnetic Resonance Imaging
Male
Medicine
Medicine & Public Health
Middle Aged
Neurology
Oncology
Radiation therapy
Retrospective Studies
Treatment Outcome
Tumor markers
Young Adult
title Incidence of high grade gliomas presenting as radiographically non-enhancing lesions: experience in 111 surgically treated non-enhancing gliomas with tissue diagnosis
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