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复发性胶质母细胞瘤的分子基础和不断发展的治疗范例。

Recurrent Glioblastoma-Molecular Underpinnings and Evolving Treatment Paradigms.

机构信息

Warren Alpert Medical School, Brown University, Providence, RI 02912, USA.

Department of Neurosurgery, Brigham and Women's Hospital, Boston, MA 02115, USA.

出版信息

Int J Mol Sci. 2024 Jun 19;25(12):6733. doi: 10.3390/ijms25126733.


DOI:10.3390/ijms25126733
PMID:38928445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11203521/
Abstract

Glioblastoma is the most common and lethal central nervous system malignancy with a median survival after progression of only 6-9 months. Major biochemical mechanisms implicated in glioblastoma recurrence include aberrant molecular pathways, a recurrence-inducing tumor microenvironment, and epigenetic modifications. Contemporary standard-of-care (surgery, radiation, chemotherapy, and tumor treating fields) helps to control the primary tumor but rarely prevents relapse. Cytoreductive treatment such as surgery has shown benefits in recurrent glioblastoma; however, its use remains controversial. Several innovative treatments are emerging for recurrent glioblastoma, including checkpoint inhibitors, chimeric antigen receptor T cell therapy, oncolytic virotherapy, nanoparticle delivery, laser interstitial thermal therapy, and photodynamic therapy. This review seeks to provide readers with an overview of (1) recent discoveries in the molecular basis of recurrence; (2) the role of surgery in treating recurrence; and (3) novel treatment paradigms emerging for recurrent glioblastoma.

摘要

胶质母细胞瘤是最常见和致命的中枢神经系统恶性肿瘤,进展后的中位生存期仅为 6-9 个月。与胶质母细胞瘤复发相关的主要生化机制包括异常的分子途径、诱导复发的肿瘤微环境和表观遗传修饰。当代的标准治疗方法(手术、放疗、化疗和肿瘤治疗电场)有助于控制原发性肿瘤,但很少能预防复发。细胞减少治疗,如手术,已显示对复发性胶质母细胞瘤有益;然而,其使用仍存在争议。几种创新的治疗方法正在出现,用于复发性胶质母细胞瘤,包括检查点抑制剂、嵌合抗原受体 T 细胞疗法、溶瘤病毒治疗、纳米颗粒递药、激光间质热疗和光动力疗法。这篇综述旨在为读者提供以下方面的概述:(1)复发分子基础的最新发现;(2)手术在治疗复发中的作用;(3)复发性胶质母细胞瘤出现的新治疗模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/11203521/1d03ac22c5f2/ijms-25-06733-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/11203521/1d03ac22c5f2/ijms-25-06733-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/11203521/1d03ac22c5f2/ijms-25-06733-g001.jpg

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本文引用的文献

[1]
Intrathecal bivalent CAR T cells targeting EGFR and IL13Rα2 in recurrent glioblastoma: phase 1 trial interim results.

Nat Med. 2024-5

[2]
Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma.

N Engl J Med. 2024-4-11

[3]
Locoregional delivery of IL-13Rα2-targeting CAR-T cells in recurrent high-grade glioma: a phase 1 trial.

Nat Med. 2024-4

[4]
Repeated peripheral infusions of anti-EGFRvIII CAR T cells in combination with pembrolizumab show no efficacy in glioblastoma: a phase 1 trial.

Nat Cancer. 2024-3

[5]
Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma.

Front Cell Dev Biol. 2023-10-4

[6]
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J Neurosurg. 2024-4-1

[7]
Clinical trial links oncolytic immunoactivation to survival in glioblastoma.

Nature. 2023-11

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Intratumoral drug-releasing microdevices allow in situ high-throughput pharmaco phenotyping in patients with gliomas.

Sci Transl Med. 2023-9-6

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Recent oncolytic virotherapy clinical trials outline a roadmap for the treatment of high-grade glioma.

Neurooncol Adv. 2023-7-7

[10]
Photodynamic Therapy for Glioblastoma: Illuminating the Path toward Clinical Applicability.

Cancers (Basel). 2023-6-30

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