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H3 K27M 突变型胶质瘤与弥漫性内生性桥脑胶质瘤:治疗格局与未来方向的半系统综述

英文原题:H3 K27M-altered glioma and diffuse intrinsic pontine glioma: Semi-systematic review of treatment landscape and future directions.

查看英文原题

H3 K27M-altered glioma and diffuse intrinsic pontine glioma: Semi-systematic review of treatment landscape and future directions.

PubMed 2024/05/03(内容时间) Neuro Oncol Q1 · IF 13.1(JCR 2025)

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中文摘要

H3 K27M突变型弥漫性胶质瘤是近期发现的一种与预后不良相关的脑肿瘤。截至2016年,世界卫生组织将其归类为一种独特的IV级胶质瘤。尽管已被认为是弥漫性胶质瘤重要的预后和诊断特征,放疗仍是唯一的标准治疗,且对于H3K27M突变型肿瘤尚无有效的全身性疗法。本综述将详述在发现H3 K27M突变之前针对弥漫性中线胶质瘤和弥漫性内生性脑桥胶质瘤(DIPG)所采用的治疗干预措施、目前H3 K27M突变型弥漫性胶质瘤治疗的标准方案,以及www.ClinicalTrials.gov上列出的正在评估该人群新型疗法的进行中的临床试验。当前临床试验通过ClinicalTrials.gov检索确定,符合本分析条件的研究为活跃或正在进行的干预性试验,这些试验在至少1个治疗组或队列中评估了一种疗法,且该组或队列完全由DIPG和H3 K27M突变型胶质瘤患者组成。共有41项研究符合这些标准,包括评估H3 K27M疫苗、CAR-T 细胞疗法和小分子抑制剂的试验。持续评估新型疗法对于在这一服务不足的患者群体中确定安全有效的干预措施是必要的。

展开英文摘要原文

H3 K27M-mutant diffuse glioma is a recently identified brain tumor associated with poor prognosis. As of 2016, it is classified by the World Health Organization as a distinct form of grade IV glioma. Despite recognition as an important prognostic and diagnostic feature in diffuse glioma, radiation remains the sole standard of care and no effective systemic therapies are available for H3K27M mutant tumors. This review will detail treatment interventions applied to diffuse midline glioma and diffuse intrinsic pontine glioma (DIPG) prior to the identification of the H3 K27M mutation, the current standard-of-care for H3 K27M-mutant diffuse glioma treatment, and ongoing clinical trials listed on www.

clinicaltrials. gov evaluating novel therapeutics in this population. Current clinical trials were identified using clinicaltrials. gov, and studies qualifying for this analysis were active or ongoing interventional trials that evaluated a therapy in at least 1 treatment arm or cohort comprised exclusively of patients with DIPG and H3 K27M-mutant glioma.

Forty-one studies met these criteria, including trials evaluating H3 K27M vaccination, chimeric antigen receptor T-cell therapy, and small molecule inhibitors. Ongoing evaluation of novel therapeutics is necessary to identify safe and effective interventions in this underserved patient population.

论文信息

作者
van den Bent M、Saratsis AM、Geurts M、Franceschi E
第一作者单位
Brain Tumor Center at Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.Netherlands
通讯作者单位
Department of Nervous System Medical Oncology, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.Italy
文献类型
综述
期刊
Neuro-oncology2024 May 3
原文标识
PubMed 38102230 · DOI 10.1093/neuonc/noad220