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本文引用的文献

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Biology (Basel). 2024 Aug 2;13(8):586. doi: 10.3390/biology13080586.
2
First step results from a phase II study of a dendritic cell vaccine in glioblastoma patients (CombiG-vax).第一步源自胶质母细胞瘤患者树突细胞疫苗(CombiG-vax)的 II 期研究结果。
Front Immunol. 2024 Aug 13;15:1404861. doi: 10.3389/fimmu.2024.1404861. eCollection 2024.
3
CAR-T and CAR-NK as cellular cancer immunotherapy for solid tumors.嵌合抗原受体 T 细胞(CAR-T)和嵌合抗原受体自然杀伤细胞(CAR-NK)作为实体瘤的细胞癌症免疫疗法。
Cell Mol Immunol. 2024 Oct;21(10):1089-1108. doi: 10.1038/s41423-024-01207-0. Epub 2024 Aug 12.
4
Macrophage polarization in the tumor microenvironment: Emerging roles and therapeutic potentials.肿瘤微环境中的巨噬细胞极化:新兴作用和治疗潜力。
Biomed Pharmacother. 2024 Aug;177:116930. doi: 10.1016/j.biopha.2024.116930. Epub 2024 Jun 14.
5
Clinical application of immunogenic cell death inducers in cancer immunotherapy: turning cold tumors hot.免疫原性细胞死亡诱导剂在癌症免疫治疗中的临床应用:将冷肿瘤变热
Front Cell Dev Biol. 2024 May 7;12:1363121. doi: 10.3389/fcell.2024.1363121. eCollection 2024.
6
Understanding the immunosuppressive microenvironment of glioma: mechanistic insights and clinical perspectives.了解胶质瘤的免疫抑制微环境:机制见解和临床观点。
J Hematol Oncol. 2024 May 8;17(1):31. doi: 10.1186/s13045-024-01544-7.
7
Dendritic Cell Vaccines: A Shift from Conventional Approach to New Generations.树突状细胞疫苗:从传统方法到新一代的转变。
Cells. 2023 Aug 25;12(17):2147. doi: 10.3390/cells12172147.
8
Whole tumour cell-based vaccines: tuning the instruments to orchestrate an optimal antitumour immune response.基于全肿瘤细胞的疫苗:调整仪器以协调最佳抗肿瘤免疫反应。
Br J Cancer. 2023 Sep;129(4):572-585. doi: 10.1038/s41416-023-02327-6. Epub 2023 Jun 24.
9
Tumor-Associated Macrophage Subsets: Shaping Polarization and Targeting.肿瘤相关巨噬细胞亚群:塑造极化和靶向。
Int J Mol Sci. 2023 Apr 19;24(8):7493. doi: 10.3390/ijms24087493.
10
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多形性胶质母细胞瘤基于癌细胞疫苗临床开发的5年进展

A 5-Year Update on the Clinical Development of Cancer Cell-Based Vaccines for Glioblastoma Multiforme.

作者信息

Alkayyal Almohanad A, Mahmoud Ahmad Bakur

机构信息

Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, University of Tabuk, Tabuk 71491, Saudi Arabia.

College of Applied Medical Sciences, Taibah University, Madinah 41477, Saudi Arabia.

出版信息

Pharmaceuticals (Basel). 2025 Mar 6;18(3):376. doi: 10.3390/ph18030376.

DOI:10.3390/ph18030376
PMID:40143152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11946125/
Abstract

Glioblastoma multiforme (GBM) is considered one of the most aggressive forms of brain cancer with a 15-month median survival, despite advancements in surgery, radiotherapy, and chemotherapy. The immune-suppressed tumor microenvironment and the blood-brain barrier are major contributors to its poor prognosis and treatment resistance. In the last decade, significant progress has been made in developing cell-based vaccines to boost immune responses against GBM. This review provides an extensive update on recent clinical trials involving various cancer cell vaccines, including ICT-107, the α-type-1 DC vaccine, and others. Although these trials have demonstrated potential improvements in progression-free survival (PFS) and overall survival (OS), the diverse and immune-suppressed nature of GBM poses challenges for consistent therapeutic success. We discuss the details of these trials along with the potential mechanism of vaccine efficacy and immune activations. The findings of these trials highlight the significance of a personalized immunotherapy approach and suggest that patient stratification could significantly advance the clinical management of GBM.

摘要

多形性胶质母细胞瘤(GBM)被认为是最具侵袭性的脑癌形式之一,尽管手术、放疗和化疗有所进展,但其中位生存期仍为15个月。免疫抑制的肿瘤微环境和血脑屏障是其预后不良和治疗耐药的主要原因。在过去十年中,在开发基于细胞的疫苗以增强针对GBM的免疫反应方面取得了重大进展。本综述广泛更新了最近涉及各种癌细胞疫苗的临床试验,包括ICT-107、α-1型树突状细胞疫苗等。尽管这些试验已证明无进展生存期(PFS)和总生存期(OS)有潜在改善,但GBM的多样性和免疫抑制性质给持续的治疗成功带来了挑战。我们讨论了这些试验的细节以及疫苗疗效和免疫激活的潜在机制。这些试验的结果突出了个性化免疫治疗方法的重要性,并表明患者分层可显著推进GBM的临床管理。