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Temozolomide resistance in glioblastoma multiforme.多形性胶质母细胞瘤中的替莫唑胺耐药性。
Genes Dis. 2016 May 11;3(3):198-210. doi: 10.1016/j.gendis.2016.04.007. eCollection 2016 Sep.
2
Combination therapy with capecitabine and temozolomide in patients with low and high grade neuroendocrine tumors, with an exploratory analysis of O-methylguanine DNA methyltransferase as a biomarker for response.卡培他滨与替莫唑胺联合治疗低级别和高级别神经内分泌肿瘤患者,并对O-甲基鸟嘌呤DNA甲基转移酶作为反应生物标志物进行探索性分析。
Oncotarget. 2017 Oct 24;8(61):104046-104056. doi: 10.18632/oncotarget.22001. eCollection 2017 Nov 28.
3
Combination treatment with recombinant methioninase enables temozolomide to arrest a BRAF V600E melanoma in a patient-derived orthotopic xenograft (PDOX) mouse model.在患者来源的原位异种移植(PDOX)小鼠模型中,重组蛋氨酸酶联合治疗可使替莫唑胺抑制BRAF V600E黑色素瘤。
Oncotarget. 2017 Aug 12;8(49):85516-85525. doi: 10.18632/oncotarget.20231. eCollection 2017 Oct 17.
4
Functional network analysis of gene-phenotype connectivity associated with temozolomide.与替莫唑胺相关的基因-表型连接性的功能网络分析
Oncotarget. 2017 Sep 12;8(50):87554-87567. doi: 10.18632/oncotarget.20848. eCollection 2017 Oct 20.
5
Multiple high-grade gliomas: epidemiology, management, and outcome. A systematic review and meta-analysis.多发性高级别胶质瘤:流行病学、管理与结局。一项系统评价和荟萃分析。
Neurosurg Rev. 2019 Jun;42(2):263-275. doi: 10.1007/s10143-017-0928-7. Epub 2017 Nov 14.
6
Optimization of IL13Rα2-Targeted Chimeric Antigen Receptor T Cells for Improved Anti-tumor Efficacy against Glioblastoma.优化针对 IL13Rα2 的嵌合抗原受体 T 细胞,以提高对神经胶质瘤的抗肿瘤疗效。
Mol Ther. 2018 Jan 3;26(1):31-44. doi: 10.1016/j.ymthe.2017.10.002. Epub 2017 Oct 5.
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Single-Cell RNA-Seq Analysis of Infiltrating Neoplastic Cells at the Migrating Front of Human Glioblastoma.单细胞 RNA 测序分析人类脑胶质瘤迁移前沿浸润性肿瘤细胞。
Cell Rep. 2017 Oct 31;21(5):1399-1410. doi: 10.1016/j.celrep.2017.10.030.
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Phase I Trial of DNX-2401 for Diffuse Intrinsic Pontine Glioma Newly Diagnosed in Pediatric Patients.儿科新诊断弥漫性内生脑桥胶质瘤患者的 DNX-2401 Ⅰ期临床试验。
Neurosurgery. 2018 Nov 1;83(5):1050-1056. doi: 10.1093/neuros/nyx507.
9
Multifunctional targeted liposomal drug delivery for efficient glioblastoma treatment.用于高效治疗胶质母细胞瘤的多功能靶向脂质体药物递送
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Integrins and Exosomes, a Dangerous Liaison in Cancer Progression.整合素与外泌体:癌症进展中的危险关联
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围攻下的胶质母细胞瘤:当前治疗策略概述

Glioblastoma under Siege: An Overview of Current Therapeutic Strategies.

作者信息

Paolillo Mayra, Boselli Cinzia, Schinelli Sergio

机构信息

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

出版信息

Brain Sci. 2018 Jan 16;8(1):15. doi: 10.3390/brainsci8010015.

DOI:10.3390/brainsci8010015
PMID:29337870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5789346/
Abstract

Glioblastoma is known to be one of the most lethal and untreatable human tumors. Surgery and radiotherapy in combination with classical alkylating agents such as temozolomide offer little hope to escape a poor prognosis. For these reasons, enormous efforts are currently devoted to refine in vivo and in vitro models with the specific goal of finding new molecular aberrant pathways, suitable to be targeted by a variety of therapeutic approaches, including novel pharmaceutical formulations and immunotherapy strategies. In this review, we will first discuss current molecular classification based on genomic and transcriptomic criteria. Also, the state of the art in current clinical practice for glioblastoma therapy in the light of the recent molecular classification, together with ongoing phases II and III clinical trials, will be described. Finally, new pharmaceutical formulations such as nanoparticles and viral vectors, together with new strategies entailing the use of monoclonal antibodies, vaccines and immunotherapy agents, such as checkpoint inhibitors, will also be discussed.

摘要

胶质母细胞瘤是已知最致命且难以治疗的人类肿瘤之一。手术、放疗以及与替莫唑胺等经典烷化剂联合使用,对于摆脱不良预后几乎没有希望。基于这些原因,目前人们投入了巨大努力来完善体内和体外模型,其具体目标是找到新的分子异常途径,这些途径适合被包括新型药物制剂和免疫治疗策略在内的多种治疗方法所靶向。在这篇综述中,我们将首先讨论基于基因组和转录组标准的当前分子分类。此外,还将描述根据最近的分子分类,胶质母细胞瘤治疗当前临床实践的现状,以及正在进行的II期和III期临床试验。最后,还将讨论纳米颗粒和病毒载体等新型药物制剂,以及涉及使用单克隆抗体、疫苗和免疫治疗药物(如检查点抑制剂)的新策略。