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溶瘤病毒疗法治疗胶质母细胞瘤的现状与挑战

英文原题:Current Status and Challenges of Oncolytic Virotherapy for the Treatment of Glioblastoma.

查看英文原题

Current Status and Challenges of Oncolytic Virotherapy for the Treatment of Glioblastoma.

PubMed 2023/05/26(内容时间) Pharmaceuticals (Basel) Q1 · IF 5.7(JCR 2025)

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中文摘要

尽管经过数十年的研究和大量临床试验,被诊断为胶质母细胞瘤(GBM)的患者预后仍然严峻,中位观察生存期为8个月。GBM是最常见的恶性原发性脑肿瘤,迫切需要新的治疗方法。癌症治疗领域的重大进展,如免疫检查点抑制剂和嵌合抗原受体(CAR)T细胞疗法,尚未改善GBM的结局。手术后继以放化疗联合或不联合肿瘤电场治疗的传统疗法仍是标准治疗。目前正在探索的众多GBM治疗方法之一是病毒疗法。这些疗法通常通过选择性裂解靶肿瘤细胞(称为溶瘤作用)或通过病毒载体靶向递送治疗性转基因来发挥作用。在这篇综述中,我们讨论了其潜在作用机制,并描述了使用这些病毒的近期和当前人体临床试验,重点关注可能最终打破该领域当前停滞范式的有前景的病毒治疗药物。

展开英文摘要原文

Despite decades of research and numerous clinical trials, the prognosis of patients diagnosed with glioblastoma (GBM) remains dire with median observed survival at 8 months. There is a critical need for novel treatments for GBM, which is the most common malignant primary brain tumor. Major advances in cancer therapeutics such as immune checkpoint inhibitors and chimeric antigen receptor (CAR) T-cell therapy have not yet led to improved outcomes for GBM. Conventional therapy of surgery followed by chemoradiation with or without tumor treating fields remains the standard of care.

One of the many approaches to GBM therapy currently being explored is viral therapies. These typically work by selectively lysing target neoplastic cells, called oncolysis, or by the targeted delivery of a therapeutic transgene via a viral vector. In this review, we discuss the underlying mechanisms of action and describe both recent and current human clinical trials using these viruses with an emphasis on promising viral therapeutics that may ultimately break the field's current stagnant paradigm.

论文信息

作者
Webb MJ、Sener U、Vile RG
第一作者单位
Department of Hematology, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USA.United States
通讯作者单位
Department of Molecular Medicine, Mayo Clinic, 200 1st Street SW, Rochester, MN 55905, USA.United States
文献类型
综述
期刊
Pharmaceuticals (Basel, Switzerland)2023 May 26
原文标识
PubMed 37375742 · DOI 10.3390/ph16060793