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
Hauptverfasser: Watanabe, Gina, Wong, Jennifer Manyu, Estes, Bradley, Khan, Mohammad Faizan, Ogasawara, Christian, Umana, Giuseppe E., Martin, Allan R., Bloch, Orin, Palmisciano, Paolo
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container_end_page 394
container_issue 3
container_start_page 379
container_title Journal of neuro-oncology
container_volume 166
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.
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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 &amp; 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. 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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 &amp; 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 ; 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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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