• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

弥漫性二级和三级胶质瘤的当前治疗方法。

Current therapeutic approaches to diffuse grade II and III gliomas.

作者信息

Picca Alberto, Berzero Giulia, Sanson Marc

机构信息

AP-HP Groupe Hospitalier Pitié-Salpêtrière, service de Neurologie 2-Mazarin, Paris, France; Neuroscience Consortium, University of Pavia, Monza Policlinico and Pavia Mondino, Italy.

AP-HP Pitié-Salpêtrière, Service de Neurologie 2-Mazarin, 47-83 Boulevard de l'Hôpital, 75013 Paris, France and Université Pierre et Marie Curie, Paris VI, Institut du Cerveau et de la Moelle Epinière, INSERM CNRS U1127, UMR 7225, Paris, France.

出版信息

Ther Adv Neurol Disord. 2018 Jan 17;11:1756285617752039. doi: 10.1177/1756285617752039. eCollection 2018.

DOI:10.1177/1756285617752039
PMID:29403544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5791552/
Abstract

The 2016 WHO classification of Tumors of the Central Nervous System brought major conceptual and practical changes in the classification of diffuse gliomas, by combining molecular features and histology into 'integrated' diagnoses. In diffuse gliomas, molecular profiling has thus become essential for nosological purposes, as well as to plan adequate treatment strategies and identify patients susceptible of target therapy. WHO grade II (low grade) and grade III (anaplastic) diffuse gliomas form a heterogeneous group of neoplasms, also known as 'lower-grade gliomas', characterized by a wide range of malignant potential. Molecular profile accounts for this biological diversity, and provides an accurate prognostic stratification of tumors in this group. Treatment strategies in lower-grade gliomas are ultimately based on molecular profile and WHO grade, as well as on patient characteristics such as age and Karnofsky performance status. The purpose of this review is to summarize recent advances in the classification of grade II and III gliomas, synthesize current treatment schemes according to molecular profile and describe ongoing research and future perspectives for the use of target therapies.

摘要

2016年世界卫生组织中枢神经系统肿瘤分类通过将分子特征和组织学结合为“综合”诊断,给弥漫性胶质瘤的分类带来了重大的概念和实践变革。在弥漫性胶质瘤中,分子谱分析因此对于疾病分类、制定适当的治疗策略以及识别适合靶向治疗的患者变得至关重要。世界卫生组织二级(低级别)和三级(间变性)弥漫性胶质瘤构成了一组异质性肿瘤,也被称为“低级别胶质瘤”,其特征是具有广泛的恶性潜能。分子谱解释了这种生物学多样性,并为该组肿瘤提供了准确的预后分层。低级别胶质瘤的治疗策略最终基于分子谱、世界卫生组织分级以及患者特征,如年龄和卡诺夫斯基功能状态。本综述的目的是总结二级和三级胶质瘤分类的最新进展,根据分子谱综合当前的治疗方案,并描述正在进行的研究以及靶向治疗应用的未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2375/5791552/8c548add3714/10.1177_1756285617752039-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2375/5791552/8c548add3714/10.1177_1756285617752039-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2375/5791552/8c548add3714/10.1177_1756285617752039-fig1.jpg

相似文献

1
Current therapeutic approaches to diffuse grade II and III gliomas.弥漫性二级和三级胶质瘤的当前治疗方法。
Ther Adv Neurol Disord. 2018 Jan 17;11:1756285617752039. doi: 10.1177/1756285617752039. eCollection 2018.
2
2021 updates to the World Health Organization classification of adult-type and pediatric-type diffuse gliomas: a clinical practice review.2021 年世界卫生组织成人型和儿童型弥漫性神经胶质瘤分类更新:临床实践综述。
Chin Clin Oncol. 2023 Feb;12(1):7. doi: 10.21037/cco-22-120.
3
Molecular classification of diffuse cerebral WHO grade II/III gliomas using genome- and transcriptome-wide profiling improves stratification of prognostically distinct patient groups.采用全基因组和转录组谱分析对弥漫性脑 WHO 分级 II/III 级神经胶质瘤进行分子分类,可改善预后不同的患者亚组的分层。
Acta Neuropathol. 2015 May;129(5):679-93. doi: 10.1007/s00401-015-1409-0. Epub 2015 Mar 18.
4
Understanding the molecular profiling of diffuse gliomas classification: A brief overview.了解弥漫性胶质瘤分类的分子特征:简要概述。
Surg Neurol Int. 2023 Jun 30;14:225. doi: 10.25259/SNI_209_2023. eCollection 2023.
5
Pediatric-type diffuse low grade gliomas: Histomolecular profile and practical approach to their integrated diagnosis according to the WHO CNS5 classification.小儿型弥漫性低级别胶质瘤:根据 WHO CNS5 分类的组织分子特征和综合诊断的实用方法。
Indian J Pathol Microbiol. 2022 May;65(Supplement):S42-S49. doi: 10.4103/ijpm.ijpm_1043_21.
6
TERT promoter mutations contribute to IDH mutations in predicting differential responses to adjuvant therapies in WHO grade II and III diffuse gliomas.端粒酶逆转录酶(TERT)启动子突变有助于异柠檬酸脱氢酶(IDH)突变预测世界卫生组织(WHO)二级和三级弥漫性胶质瘤对辅助治疗的不同反应。
Oncotarget. 2015 Sep 22;6(28):24871-83. doi: 10.18632/oncotarget.4549.
7
Histologic classification of gliomas.胶质瘤的组织学分类。
Handb Clin Neurol. 2016;134:71-95. doi: 10.1016/B978-0-12-802997-8.00005-0.
8
Diagnostic algorithm for pathological evaluation of gliomas in a resource-constrained setting.资源受限环境下神经胶质瘤病理评估的诊断算法
J Cancer Res Ther. 2023 Apr-Jun;19(3):562-566. doi: 10.4103/jcrt.jcrt_102_21.
9
The Misclassification of Diffuse Gliomas: Rates and Outcomes.弥漫性神经胶质瘤的误诊:发生率与结局。
Clin Cancer Res. 2019 Apr 15;25(8):2656-2663. doi: 10.1158/1078-0432.CCR-18-3101. Epub 2019 Jan 11.
10
Review on neuroimaging in pediatric-type diffuse low-grade gliomas.儿童型弥漫性低级别胶质瘤的神经影像学综述
Front Pediatr. 2023 Oct 18;11:1149646. doi: 10.3389/fped.2023.1149646. eCollection 2023.

引用本文的文献

1
Identification of DNA methylation-regulated WEE1 with potential implications in prognosis and immunotherapy for low-grade glioma.鉴定 DNA 甲基化调控的 WEE1,其对低级别胶质瘤的预后和免疫治疗具有潜在意义。
Cancer Biomark. 2024;40(3-4):297-317. doi: 10.3233/CBM-230517.
2
Neurophysiotherapy in Grade II Diffuse Astrocytoma: A Case Report.II级弥漫性星形细胞瘤的神经物理治疗:一例报告
Cureus. 2024 Jan 27;16(1):e53082. doi: 10.7759/cureus.53082. eCollection 2024 Jan.
3
Genetic profiling of rat gliomas and cardiac schwannomas from life-time radiofrequency radiation exposure study using a targeted next-generation sequencing gene panel.

本文引用的文献

1
Interim results from the CATNON trial (EORTC study 26053-22054) of treatment with concurrent and adjuvant temozolomide for 1p/19q non-co-deleted anaplastic glioma: a phase 3, randomised, open-label intergroup study.CATNON 试验(EORTC 研究 26053-22054)的中期结果,该试验采用同步和辅助替莫唑胺治疗 1p/19q 非共缺失间变性神经胶质瘤:一项 3 期、随机、开放标签的分组间研究。
Lancet. 2017 Oct 7;390(10103):1645-1653. doi: 10.1016/S0140-6736(17)31442-3. Epub 2017 Aug 8.
2
Diffuse Infiltrating Oligodendroglioma and Astrocytoma.弥漫性浸润性少突胶质细胞瘤和星形细胞瘤。
J Clin Oncol. 2017 Jul 20;35(21):2394-2401. doi: 10.1200/JCO.2017.72.6737. Epub 2017 Jun 22.
3
利用靶向下一代测序基因 panel 对终生射频辐射暴露研究中的大鼠神经胶质瘤和心脏施万细胞瘤进行遗传分析。
PLoS One. 2024 Jan 17;19(1):e0296699. doi: 10.1371/journal.pone.0296699. eCollection 2024.
4
The effect Of vascular related CeRNA genes and corresponding imaging biomarkers on survival in lower grade glioma.血管相关 ceRNA 基因及其相应的影像生物标志物对低级别胶质瘤患者生存的影响。
Ir J Med Sci. 2024 Apr;193(2):653-663. doi: 10.1007/s11845-023-03536-x. Epub 2023 Oct 6.
5
Grade scoring system reveals distinct molecular subtypes and identifies KIF20A as a novel biomarker for predicting temozolomide treatment efficiency in gliomas.分级评分系统揭示了不同的分子亚型,并将KIF20A鉴定为预测胶质瘤替莫唑胺治疗疗效的新型生物标志物。
J Cancer Res Clin Oncol. 2023 Sep;149(12):9857-9876. doi: 10.1007/s00432-023-04898-6. Epub 2023 May 29.
6
LUMOS - Low and Intermediate Grade Glioma Umbrella Study of Molecular Guided TherapieS at relapse: Protocol for a pilot study.LUMOS 研究:复发性低级别和中级别神经胶质瘤分子靶向治疗的伞式研究:一项初步研究的方案。
BMJ Open. 2021 Dec 30;11(12):e054075. doi: 10.1136/bmjopen-2021-054075.
7
Postoperative prognostic nomogram for adult grade II/III astrocytoma in the Chinese Han population.中国汉族人群成人II/III级星形细胞瘤术后预后列线图
Health Inf Sci Syst. 2023 May 4;11(1):23. doi: 10.1007/s13755-023-00223-0. eCollection 2023 Dec.
8
A Handheld Visible Resonance Raman Analyzer Used in Intraoperative Detection of Human Glioma.一种用于术中检测人脑胶质瘤的手持式可见共振拉曼分析仪。
Cancers (Basel). 2023 Mar 14;15(6):1752. doi: 10.3390/cancers15061752.
9
A novel risk score model based on fourteen chromatin regulators-based genes for predicting overall survival of patients with lower-grade gliomas.一种基于14个染色质调节因子相关基因的新型风险评分模型,用于预测低级别胶质瘤患者的总生存期。
Front Genet. 2022 Sep 26;13:957059. doi: 10.3389/fgene.2022.957059. eCollection 2022.
10
Molecular Aberrations Stratify Grade 2 Astrocytomas Into Several Rare Entities: Prognostic and Therapeutic Implications.分子异常将2级星形细胞瘤分为几种罕见实体:对预后和治疗的影响
Front Oncol. 2022 Jun 10;12:866623. doi: 10.3389/fonc.2022.866623. eCollection 2022.
Identifying clinical risk in low grade gliomas and appropriate treatment strategies, with special emphasis on the role of surgery.
识别低级别胶质瘤的临床风险及合适的治疗策略,特别强调手术的作用。
Expert Rev Anticancer Ther. 2017 Aug;17(8):703-716. doi: 10.1080/14737140.2017.1342537. Epub 2017 Jun 28.
4
European Association for Neuro-Oncology (EANO) guideline on the diagnosis and treatment of adult astrocytic and oligodendroglial gliomas.欧洲神经肿瘤学会(EANO)成人星形细胞瘤和少突胶质细胞瘤诊断和治疗指南。
Lancet Oncol. 2017 Jun;18(6):e315-e329. doi: 10.1016/S1470-2045(17)30194-8. Epub 2017 May 5.
5
Surgical resection versus watchful waiting in low-grade gliomas.低级别胶质瘤的手术切除与观察等待。
Ann Oncol. 2017 Aug 1;28(8):1942-1948. doi: 10.1093/annonc/mdx230.
6
Biopsy versus resection for the management of low-grade gliomas.活检与手术切除用于低级别胶质瘤的治疗比较
Cochrane Database Syst Rev. 2017 Apr 27;4(4):CD009319. doi: 10.1002/14651858.CD009319.pub3.
7
Mutational burden, immune checkpoint expression, and mismatch repair in glioma: implications for immune checkpoint immunotherapy.胶质瘤中的突变负担、免疫检查点表达和错配修复:对免疫检查点免疫治疗的影响。
Neuro Oncol. 2017 Aug 1;19(8):1047-1057. doi: 10.1093/neuonc/nox026.
8
Chemosensitivity of IDH1-Mutated Gliomas Due to an Impairment in PARP1-Mediated DNA Repair.异柠檬酸脱氢酶1(IDH1)突变型胶质瘤因聚(ADP-核糖)聚合酶1(PARP1)介导的DNA修复受损而产生的化学敏感性。
Cancer Res. 2017 Apr 1;77(7):1709-1718. doi: 10.1158/0008-5472.CAN-16-2773. Epub 2017 Feb 15.
9
Supratotal resection of diffuse gliomas - an overview of its multifaceted implications.弥漫性胶质瘤的超全切除——多方面影响概述
Neurochirurgie. 2017 Jun;63(3):243-249. doi: 10.1016/j.neuchi.2016.09.006. Epub 2017 Feb 7.
10
2-Hydroxyglutarate produced by neomorphic IDH mutations suppresses homologous recombination and induces PARP inhibitor sensitivity.由新形态异柠檬酸脱氢酶(IDH)突变产生的2-羟基戊二酸抑制同源重组并诱导对聚(ADP-核糖)聚合酶(PARP)抑制剂的敏感性。
Sci Transl Med. 2017 Feb 1;9(375). doi: 10.1126/scitranslmed.aal2463.