Diffuse Midline H3K27-Altered Gliomas in the Spinal Cord: A Systematic Review
Purpose To systematically review the clinical features, management, and outcomes of diffuse midline H3K27-altered gliomas of the spinal cord (DMG-SCs). Methods PubMed, Ovid EMBASE, Scopus, and Web of Science were searched from database inception to 23 September 2023 for histologically confirmed case...
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Veröffentlicht in: | Journal of neuro-oncology 2024-02, Vol.166 (3), p.379-394 |
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creator | Watanabe, Gina Wong, Jennifer Manyu Estes, Bradley Khan, Mohammad Faizan Ogasawara, Christian Umana, Giuseppe E. Martin, Allan R. Bloch, Orin Palmisciano, Paolo |
description | Purpose
To systematically review the clinical features, management, and outcomes of diffuse midline H3K27-altered gliomas of the spinal cord (DMG-SCs).
Methods
PubMed, Ovid EMBASE, Scopus, and Web of Science were searched from database inception to 23 September 2023 for histologically confirmed cases of DMG-SC. Patient demographics, tumor characteristics, management information, and survival outcomes were extracted and analyzed.
Results
A total of 279 patients from 39 studies were collected. Patients were mostly male (61%), with an average age of 32 years. Patients were treated with surgery, radiotherapy, and chemotherapy combined (31%) or surgery only (24%), and extent of resection was most often subtotal (38%). Temozolomide was the most common chemotherapeutic agent (81%). Radiation therapy was delivered with mean dose of 47 Gy in 23 fractions. At mean follow-up time of 21 months, 13% of patients were alive. Average median overall survival was 24 months (range of 13 to 40 months) with a median progression-free survival of 14 months. Historical WHO grades of 2 or 3 appeared to exhibit a longer average median overall survival time than that of grade 4 DMG-SCs (32 vs. 23 months, p = 0.009).
Conclusions
Outcomes for DMG-SCs are poor overall but appear to be favorable compared to intracranial DMGs. Despite the recent WHO 2021 grade 4 classification for all DMGs, given the differences in overall survival reported based on historical grading systems, future studies on DMG-SCs are needed to further define if DMG-SCs may represent a heterogeneous group of tumors with different prognoses. |
doi_str_mv | 10.1007/s11060-024-04584-8 |
format | Article |
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To systematically review the clinical features, management, and outcomes of diffuse midline H3K27-altered gliomas of the spinal cord (DMG-SCs).
Methods
PubMed, Ovid EMBASE, Scopus, and Web of Science were searched from database inception to 23 September 2023 for histologically confirmed cases of DMG-SC. Patient demographics, tumor characteristics, management information, and survival outcomes were extracted and analyzed.
Results
A total of 279 patients from 39 studies were collected. Patients were mostly male (61%), with an average age of 32 years. Patients were treated with surgery, radiotherapy, and chemotherapy combined (31%) or surgery only (24%), and extent of resection was most often subtotal (38%). Temozolomide was the most common chemotherapeutic agent (81%). Radiation therapy was delivered with mean dose of 47 Gy in 23 fractions. At mean follow-up time of 21 months, 13% of patients were alive. Average median overall survival was 24 months (range of 13 to 40 months) with a median progression-free survival of 14 months. Historical WHO grades of 2 or 3 appeared to exhibit a longer average median overall survival time than that of grade 4 DMG-SCs (32 vs. 23 months, p = 0.009).
Conclusions
Outcomes for DMG-SCs are poor overall but appear to be favorable compared to intracranial DMGs. Despite the recent WHO 2021 grade 4 classification for all DMGs, given the differences in overall survival reported based on historical grading systems, future studies on DMG-SCs are needed to further define if DMG-SCs may represent a heterogeneous group of tumors with different prognoses.</description><identifier>ISSN: 0167-594X</identifier><identifier>ISSN: 1573-7373</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1007/s11060-024-04584-8</identifier><identifier>PMID: 38342826</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Brain tumors ; Chemotherapy ; Glioma ; Glioma - mortality ; Glioma - pathology ; Glioma - therapy ; Histones - genetics ; Histones - metabolism ; Humans ; Medicine ; Medicine & Public Health ; Neurology ; Oncology ; Patients ; Prognosis ; Radiation therapy ; Review ; Spinal cord ; Spinal Cord Neoplasms - pathology ; Spinal Cord Neoplasms - therapy ; Surgery ; Survival ; Temozolomide</subject><ispartof>Journal of neuro-oncology, 2024-02, Vol.166 (3), p.379-394</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-8a1767732510f74a519a545281237b2493a9b7f0f644ab03b80a03d95387f4ed3</citedby><cites>FETCH-LOGICAL-c375t-8a1767732510f74a519a545281237b2493a9b7f0f644ab03b80a03d95387f4ed3</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/s11060-024-04584-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11060-024-04584-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38342826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Watanabe, Gina</creatorcontrib><creatorcontrib>Wong, Jennifer Manyu</creatorcontrib><creatorcontrib>Estes, Bradley</creatorcontrib><creatorcontrib>Khan, Mohammad Faizan</creatorcontrib><creatorcontrib>Ogasawara, Christian</creatorcontrib><creatorcontrib>Umana, Giuseppe E.</creatorcontrib><creatorcontrib>Martin, Allan R.</creatorcontrib><creatorcontrib>Bloch, Orin</creatorcontrib><creatorcontrib>Palmisciano, Paolo</creatorcontrib><title>Diffuse Midline H3K27-Altered Gliomas in the Spinal Cord: A Systematic Review</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><addtitle>J Neurooncol</addtitle><description>Purpose
To systematically review the clinical features, management, and outcomes of diffuse midline H3K27-altered gliomas of the spinal cord (DMG-SCs).
Methods
PubMed, Ovid EMBASE, Scopus, and Web of Science were searched from database inception to 23 September 2023 for histologically confirmed cases of DMG-SC. Patient demographics, tumor characteristics, management information, and survival outcomes were extracted and analyzed.
Results
A total of 279 patients from 39 studies were collected. Patients were mostly male (61%), with an average age of 32 years. Patients were treated with surgery, radiotherapy, and chemotherapy combined (31%) or surgery only (24%), and extent of resection was most often subtotal (38%). Temozolomide was the most common chemotherapeutic agent (81%). Radiation therapy was delivered with mean dose of 47 Gy in 23 fractions. At mean follow-up time of 21 months, 13% of patients were alive. Average median overall survival was 24 months (range of 13 to 40 months) with a median progression-free survival of 14 months. Historical WHO grades of 2 or 3 appeared to exhibit a longer average median overall survival time than that of grade 4 DMG-SCs (32 vs. 23 months, p = 0.009).
Conclusions
Outcomes for DMG-SCs are poor overall but appear to be favorable compared to intracranial DMGs. Despite the recent WHO 2021 grade 4 classification for all DMGs, given the differences in overall survival reported based on historical grading systems, future studies on DMG-SCs are needed to further define if DMG-SCs may represent a heterogeneous group of tumors with different prognoses.</description><subject>Brain tumors</subject><subject>Chemotherapy</subject><subject>Glioma</subject><subject>Glioma - mortality</subject><subject>Glioma - pathology</subject><subject>Glioma - therapy</subject><subject>Histones - genetics</subject><subject>Histones - metabolism</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurology</subject><subject>Oncology</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Radiation therapy</subject><subject>Review</subject><subject>Spinal cord</subject><subject>Spinal Cord Neoplasms - pathology</subject><subject>Spinal Cord Neoplasms - therapy</subject><subject>Surgery</subject><subject>Survival</subject><subject>Temozolomide</subject><issn>0167-594X</issn><issn>1573-7373</issn><issn>1573-7373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PGzEQhq0KVAL0D_SALHHh4jL22Gtvb1GAUBVUqaFSb5Y3622N9iPYu6D8e5YkLRIHTnOY531H8xDymcMXDqDPE-eQAQMhGUhlJDMfyIQrjUyjxj0yAZ5ppnL5-4AcpnQPAFIj_0gO0KAURmQTcnsRqmpInt6Gsg6tp9f4XWg2rXsffUnndegal2hoaf_X08UqtK6msy6WX-mULtap943rw5L-9I_BPx2T_crVyX_azSPy6-rybnbNbn7Mv82mN2yJWvXMOK4zrVEoDpWWTvHcKamE4QJ1IWSOLi90BVUmpSsACwMOsMwVGl1JX-IROdv2rmL3MPjU2yakpa9r1_puSFbkQkmDGeCInr5B77shjl9sKCOVBM5HSmypZexSir6yqxgaF9eWg32Rbbey7SjbbmRbM4ZOdtVD0fjyf-Sf3RHALZDGVfvHx9fb79Q-A-zZhck</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Watanabe, Gina</creator><creator>Wong, Jennifer Manyu</creator><creator>Estes, Bradley</creator><creator>Khan, Mohammad Faizan</creator><creator>Ogasawara, Christian</creator><creator>Umana, Giuseppe E.</creator><creator>Martin, Allan R.</creator><creator>Bloch, Orin</creator><creator>Palmisciano, Paolo</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>7TK</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20240201</creationdate><title>Diffuse Midline H3K27-Altered Gliomas in the Spinal Cord: A Systematic Review</title><author>Watanabe, Gina ; Wong, Jennifer Manyu ; Estes, Bradley ; Khan, Mohammad Faizan ; Ogasawara, Christian ; Umana, Giuseppe E. ; Martin, Allan R. ; Bloch, Orin ; Palmisciano, Paolo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-8a1767732510f74a519a545281237b2493a9b7f0f644ab03b80a03d95387f4ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Brain tumors</topic><topic>Chemotherapy</topic><topic>Glioma</topic><topic>Glioma - mortality</topic><topic>Glioma - pathology</topic><topic>Glioma - therapy</topic><topic>Histones - genetics</topic><topic>Histones - metabolism</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neurology</topic><topic>Oncology</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Radiation therapy</topic><topic>Review</topic><topic>Spinal cord</topic><topic>Spinal Cord Neoplasms - pathology</topic><topic>Spinal Cord Neoplasms - therapy</topic><topic>Surgery</topic><topic>Survival</topic><topic>Temozolomide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Watanabe, Gina</creatorcontrib><creatorcontrib>Wong, Jennifer Manyu</creatorcontrib><creatorcontrib>Estes, Bradley</creatorcontrib><creatorcontrib>Khan, Mohammad Faizan</creatorcontrib><creatorcontrib>Ogasawara, Christian</creatorcontrib><creatorcontrib>Umana, Giuseppe E.</creatorcontrib><creatorcontrib>Martin, Allan R.</creatorcontrib><creatorcontrib>Bloch, Orin</creatorcontrib><creatorcontrib>Palmisciano, Paolo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neuro-oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Watanabe, Gina</au><au>Wong, Jennifer Manyu</au><au>Estes, Bradley</au><au>Khan, Mohammad Faizan</au><au>Ogasawara, Christian</au><au>Umana, Giuseppe E.</au><au>Martin, Allan R.</au><au>Bloch, Orin</au><au>Palmisciano, Paolo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diffuse Midline H3K27-Altered Gliomas in the Spinal Cord: A Systematic Review</atitle><jtitle>Journal of neuro-oncology</jtitle><stitle>J Neurooncol</stitle><addtitle>J Neurooncol</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>166</volume><issue>3</issue><spage>379</spage><epage>394</epage><pages>379-394</pages><issn>0167-594X</issn><issn>1573-7373</issn><eissn>1573-7373</eissn><abstract>Purpose
To systematically review the clinical features, management, and outcomes of diffuse midline H3K27-altered gliomas of the spinal cord (DMG-SCs).
Methods
PubMed, Ovid EMBASE, Scopus, and Web of Science were searched from database inception to 23 September 2023 for histologically confirmed cases of DMG-SC. Patient demographics, tumor characteristics, management information, and survival outcomes were extracted and analyzed.
Results
A total of 279 patients from 39 studies were collected. Patients were mostly male (61%), with an average age of 32 years. Patients were treated with surgery, radiotherapy, and chemotherapy combined (31%) or surgery only (24%), and extent of resection was most often subtotal (38%). Temozolomide was the most common chemotherapeutic agent (81%). Radiation therapy was delivered with mean dose of 47 Gy in 23 fractions. At mean follow-up time of 21 months, 13% of patients were alive. Average median overall survival was 24 months (range of 13 to 40 months) with a median progression-free survival of 14 months. Historical WHO grades of 2 or 3 appeared to exhibit a longer average median overall survival time than that of grade 4 DMG-SCs (32 vs. 23 months, p = 0.009).
Conclusions
Outcomes for DMG-SCs are poor overall but appear to be favorable compared to intracranial DMGs. Despite the recent WHO 2021 grade 4 classification for all DMGs, given the differences in overall survival reported based on historical grading systems, future studies on DMG-SCs are needed to further define if DMG-SCs may represent a heterogeneous group of tumors with different prognoses.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>38342826</pmid><doi>10.1007/s11060-024-04584-8</doi><tpages>16</tpages></addata></record> |
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subjects | Brain tumors Chemotherapy Glioma Glioma - mortality Glioma - pathology Glioma - therapy Histones - genetics Histones - metabolism Humans Medicine Medicine & Public Health Neurology Oncology Patients Prognosis Radiation therapy Review Spinal cord Spinal Cord Neoplasms - pathology Spinal Cord Neoplasms - therapy Surgery Survival Temozolomide |
title | Diffuse Midline H3K27-Altered Gliomas in the Spinal Cord: A Systematic Review |
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