人原发性脑肿瘤免疫治疗的临床研究

Zahraa I Khamis, Nancy Al-Akkary, Timothy Hua, Sophia A. Draughon, Yan Li, Q. Sang
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引用次数: 2

摘要

人类原发性脑癌是临床上最具致命性和挑战性的恶性肿瘤之一。传统疗法无法缓解其不良后果,这促使人们努力寻找创新疗法。最近在各种实体肿瘤的免疫治疗方面取得的突破使免疫治疗成为脑癌治疗的支柱。然而,脑恶性肿瘤的独特特征,包括肿瘤内异质性、免疫抑制微环境和不透水的血脑屏障,阻碍了免疫治疗方法的成功。然而,关于肿瘤驱动的特异性免疫细胞富集的开创性发现为利用免疫细胞对抗癌症提供了新的见解。本文讨论了人脑的解剖学、微环境和免疫生物学特征,并概述了针对原发性脑癌患者的免疫疗法,特别强调了注册的2期、3期和组合临床试验。免疫检查点抑制剂、免疫细胞疗法、癌症疫苗、溶瘤病毒疗法和联合疗法在治疗人类脑肿瘤的临床环境中进行了研究。尽管偶尔会出现不良反应,但免疫靶向治疗为原发性脑癌患者提供了一个有希望的机会,以提高生存率和改善预后。哈米斯等人。神经免疫学[j]; 2020;7:[在线第一]I http://dx.doi.org/10.20517/2347-8659.2020.43
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Clinical investigations of immunotherapy for human primary brain tumors
Human primary brain cancer is one of the most lethal and clinically challenging malignancies. The failure of conventional therapies to alleviate its poor outcome has prompted efforts to find innovative treatments. Recent breakthroughs in immunotherapy across a variety of solid tumors have set immune-based therapeutics as a pillar for brain cancer treatment. However, the unique features of brain malignancies including intratumoral heterogeneity, immunosuppressive microenvironment, and impervious blood-brain barrier, thwart the success of immunotherapeutic approaches. Yet, seminal findings regarding tumor-driven enrichment of specific immune cells granted the field novel insights to harness the immune cells to fight cancer. This review discusses the anatomical, microenvironmental, and immunobiological features of the human brain and presents an overview of immunotherapies tested for primary brain cancer patients with a special emphasis on registered phase 2, 3, and combinatorial clinical trials. Immune checkpoint inhibitors, immune cell-based therapies, cancer vaccines, oncolytic viral therapy, and combination therapies are investigated in clinical settings for the treatment of human brain tumors. Despite their occasional adverse effects, immune-targeted therapies provide a promising opportunity for primary brain cancer patients to enhance survival and improve prognosis. Page 2 Khamis et al. Neuroimmunol Neuroinflammation 2020;7:[Online First] I http://dx.doi.org/10.20517/2347-8659.2020.43
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