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Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing
BACKGROUND: Grade 2/3 meningiomas have locally aggressive behaviors often requiring additional treatment plans after surgical resection. Herein, we explored the clinical significance of next-generation sequencing (NGS) in characterizing the molecular profiles of high-grade meningiomas. METHODS: Pati...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236884/ https://www.ncbi.nlm.nih.gov/pubmed/35774130 http://dx.doi.org/10.3389/fonc.2022.885155 |
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author | Kim, Junhyung Hwang, Kihwan Kwon, Hyun Jung Lee, Ji Eun Lee, Kyu Sang Choe, Gheeyoung Han, Jung Ho Kim, Chae-Yong |
author_facet | Kim, Junhyung Hwang, Kihwan Kwon, Hyun Jung Lee, Ji Eun Lee, Kyu Sang Choe, Gheeyoung Han, Jung Ho Kim, Chae-Yong |
author_sort | Kim, Junhyung |
collection | PubMed |
description | BACKGROUND: Grade 2/3 meningiomas have locally aggressive behaviors often requiring additional treatment plans after surgical resection. Herein, we explored the clinical significance of next-generation sequencing (NGS) in characterizing the molecular profiles of high-grade meningiomas. METHODS: Patients with intracranial meningioma who underwent surgical resection in a single institution were retrospectively reviewed. Clinicopathologic relevance was evaluated using recurrence-free survival (RFS) as an outcome measure. NGS for the targeted gene regions was performed in 40 participants. RESULTS: Among the 713 individuals in the study population, 143 cases (20.1%) were identified as having grade 2 or 3 meningiomas with a significantly lower female predominance. While the difference in RFS between grade 2 and 3 meningiomas was insignificant, a few conventional grade 2 cases, but with TERT promoter hotspot mutation, were highly progressive and refractory to the treatment. From the NGS study, recurrent mutations in TRAF and AKT1 were identified with a higher prevalence (17.5% and 12.5%, respectively) compared with grade 2/3 meningiomas reported in previous literature. However, their relations to other histopathologic properties or clinical factors were rarely observed. CONCLUSIONS: Grade 2/3 meningiomas show a broad spectrum of molecular profiles, as they have heterogeneous histologic characteristics. |
format | Online Article Text |
id | pubmed-9236884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92368842022-06-29 Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing Kim, Junhyung Hwang, Kihwan Kwon, Hyun Jung Lee, Ji Eun Lee, Kyu Sang Choe, Gheeyoung Han, Jung Ho Kim, Chae-Yong Front Oncol Oncology BACKGROUND: Grade 2/3 meningiomas have locally aggressive behaviors often requiring additional treatment plans after surgical resection. Herein, we explored the clinical significance of next-generation sequencing (NGS) in characterizing the molecular profiles of high-grade meningiomas. METHODS: Patients with intracranial meningioma who underwent surgical resection in a single institution were retrospectively reviewed. Clinicopathologic relevance was evaluated using recurrence-free survival (RFS) as an outcome measure. NGS for the targeted gene regions was performed in 40 participants. RESULTS: Among the 713 individuals in the study population, 143 cases (20.1%) were identified as having grade 2 or 3 meningiomas with a significantly lower female predominance. While the difference in RFS between grade 2 and 3 meningiomas was insignificant, a few conventional grade 2 cases, but with TERT promoter hotspot mutation, were highly progressive and refractory to the treatment. From the NGS study, recurrent mutations in TRAF and AKT1 were identified with a higher prevalence (17.5% and 12.5%, respectively) compared with grade 2/3 meningiomas reported in previous literature. However, their relations to other histopathologic properties or clinical factors were rarely observed. CONCLUSIONS: Grade 2/3 meningiomas show a broad spectrum of molecular profiles, as they have heterogeneous histologic characteristics. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9236884/ /pubmed/35774130 http://dx.doi.org/10.3389/fonc.2022.885155 Text en Copyright © 2022 Kim, Hwang, Kwon, Lee, Lee, Choe, Han and Kim https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Kim, Junhyung Hwang, Kihwan Kwon, Hyun Jung Lee, Ji Eun Lee, Kyu Sang Choe, Gheeyoung Han, Jung Ho Kim, Chae-Yong Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing |
title | Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing |
title_full | Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing |
title_fullStr | Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing |
title_full_unstemmed | Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing |
title_short | Clinicopathologic Characteristics of Grade 2/3 Meningiomas: A Perspective on the Role of Next-Generation Sequencing |
title_sort | clinicopathologic characteristics of grade 2/3 meningiomas: a perspective on the role of next-generation sequencing |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236884/ https://www.ncbi.nlm.nih.gov/pubmed/35774130 http://dx.doi.org/10.3389/fonc.2022.885155 |
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