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本文引用的文献

1
The first-in-human phase I study of a brain-penetrant mutant IDH1 inhibitor DS-1001 in patients with recurrent or progressive IDH1-mutant gliomas.在复发性或进行性 IDH1 突变型神经胶质瘤患者中进行的脑穿透性突变 IDH1 抑制剂 DS-1001 的首次人体 I 期研究。
Neuro Oncol. 2023 Feb 14;25(2):326-336. doi: 10.1093/neuonc/noac155.
2
Restoration of Temozolomide Sensitivity by PARP Inhibitors in Mismatch Repair Deficient Glioblastoma is Independent of Base Excision Repair.错配修复缺陷型胶质母细胞瘤中 PARP 抑制剂恢复替莫唑胺敏感性与碱基切除修复无关。
Clin Cancer Res. 2020 Apr 1;26(7):1690-1699. doi: 10.1158/1078-0432.CCR-19-2000. Epub 2020 Jan 3.
3
CDKN2A homozygous deletion is a strong adverse prognosis factor in diffuse malignant IDH-mutant gliomas.CDKN2A 纯合缺失是弥漫性恶性 IDH 突变型神经胶质瘤的一个强烈不良预后因素。
Neuro Oncol. 2019 Dec 17;21(12):1519-1528. doi: 10.1093/neuonc/noz124.
4
Longitudinal molecular trajectories of diffuse glioma in adults.成人弥漫性神经胶质瘤的纵向分子轨迹。
Nature. 2019 Dec;576(7785):112-120. doi: 10.1038/s41586-019-1775-1. Epub 2019 Nov 20.
5
CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2012-2016.美国 2012-2016 年诊断的原发性脑和其他中枢神经系统肿瘤 CBTRUS 统计报告。
Neuro Oncol. 2019 Nov 1;21(Suppl 5):v1-v100. doi: 10.1093/neuonc/noz150.
6
Management of low-grade glioma: a systematic review and meta-analysis.低级别胶质瘤的管理:一项系统综述和荟萃分析。
Neurooncol Pract. 2019 Jul;6(4):249-258. doi: 10.1093/nop/npy034. Epub 2018 Aug 18.
7
Genomic Correlates of Disease Progression and Treatment Response in Prospectively Characterized Gliomas.前瞻性特征化胶质瘤的疾病进展和治疗反应的基因组相关性。
Clin Cancer Res. 2019 Sep 15;25(18):5537-5547. doi: 10.1158/1078-0432.CCR-19-0032. Epub 2019 Jul 1.
8
Clinical pharmacokinetics and pharmacodynamics of ivosidenib, an oral, targeted inhibitor of mutant IDH1, in patients with advanced solid tumors.ivosidenib 的临床药代动力学和药效学:一种口服、针对突变 IDH1 的靶向抑制剂,用于治疗晚期实体瘤患者。
Invest New Drugs. 2020 Apr;38(2):433-444. doi: 10.1007/s10637-019-00771-x. Epub 2019 Apr 26.
9
PARP Inhibitors for Sensitization of Alkylation Chemotherapy in Glioblastoma: Impact of Blood-Brain Barrier and Molecular Heterogeneity.PARP抑制剂用于胶质母细胞瘤中烷化剂化疗的增敏作用:血脑屏障和分子异质性的影响
Front Oncol. 2019 Jan 22;8:670. doi: 10.3389/fonc.2018.00670. eCollection 2018.
10
Transaminase Inhibition by 2-Hydroxyglutarate Impairs Glutamate Biosynthesis and Redox Homeostasis in Glioma.2-羟戊二酸抑制转氨基作用可损害脑胶质瘤中的谷氨酸合成和氧化还原稳态。
Cell. 2018 Sep 20;175(1):101-116.e25. doi: 10.1016/j.cell.2018.08.038. Epub 2018 Sep 13.

低级别胶质瘤。

Lower Grade Gliomas.

机构信息

Pappas Center for Neuro-Oncology, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Curr Neurol Neurosci Rep. 2020 May 22;20(7):21. doi: 10.1007/s11910-020-01040-8.

DOI:10.1007/s11910-020-01040-8
PMID:32444979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7244462/
Abstract

PURPOSE OF REVIEW

Low-grade gliomas (LGG) are a group of primary brain tumors that arise from supporting glial cells. They are characterized by a mutation in the isocitrate dehydrogenase (IDH) enzyme and include astrocytomas and oligodendrogliomas. They usually affect young adults, and their main treatment consists of surgical resection, followed by radiation and chemotherapy in selected patients. This article reviews recent research on the clinical and molecular aspects of the disease and innovative therapeutic modalities in the process.

RECENT FINDINGS

Newly identified clinical and molecular features are currently used in the classification of LGG and applied in treatment-planning decisions. Advanced studies on the cellular level have an advanced understanding of the metabolic effects induced by IDH mutations, offering opportunities for specific targeted therapies that may improve patient outcomes. Such findings may lead to a paradigm shift in the treatment of these tumors. Although LGG are sensitive to radiation and chemotherapy, these therapies are not curative, and patient survival remains limited, raising the need for more creative and effective interventions.

摘要

目的综述

低级别胶质瘤(LGG)是一组起源于神经胶质细胞的原发性脑肿瘤。它们的特征是异柠檬酸脱氢酶(IDH)酶的突变,包括星形细胞瘤和少突胶质细胞瘤。它们通常影响年轻人,其主要治疗方法包括手术切除,然后在选定的患者中进行放疗和化疗。本文综述了该疾病的临床和分子方面以及该过程中的创新治疗方法的最新研究进展。

最新发现

目前在 LGG 的分类中使用新确定的临床和分子特征,并应用于治疗计划决策。在细胞水平上的深入研究深入了解了 IDH 突变引起的代谢效应,为可能改善患者预后的特定靶向治疗提供了机会。这些发现可能会导致这些肿瘤治疗的范式转变。尽管 LGG 对放疗和化疗敏感,但这些疗法并不能治愈,患者的生存仍然受到限制,这就需要更有创意和更有效的干预措施。