CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Clinical Applications of Immunotherapy for Recurrent Glioblastoma in Adults.
Clinical Applications of Immunotherapy for Recurrent Glioblastoma in Adults.
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胶质母细胞瘤(GBM)是成人中最常见的恶性原发性脑肿瘤。尽管采用了包括手术切除和放化疗在内的标准治疗,复发几乎不可避免。复发性胶质母细胞瘤(rGBM)的当前治疗正在迅速发展,针对原发性GBM的新兴疗法通常首先在rGBM中进行测试,以证明安全性和可行性,近年来这主要以免疫治疗的形式出现。本综述的目的是强调rGBM免疫治疗临床试验的进展,包括免疫检查点阻断、溶瘤病毒治疗、嵌合抗原受体(CAR)T细胞治疗、癌症疫苗和免疫毒素。三位独立评审员涵盖了2000年至2022年间在各种在线数据库中发表的文献。
总体而言,免疫治疗在rGBM中的疗效仍不确定,且仅限于部分患者亚群/小队列,尽管在早期临床试验中已证明其可行性。然而,在理解可能阻碍rGBM患者对免疫治疗产生反应的机制方面,以及在开发可能激发对该毁灭性疾病免疫治疗应用乐观情绪的新方法/联合策略方面,已取得了相当大的进展。需要继续开展试验,以进一步评估最佳治疗途径,并确定哪些治疗可能使每位患者个体获益。
Glioblastoma (GBM) is the most common malignant primary brain tumor in adults. Despite standard therapies, including resection and chemoradiation, recurrence is virtually inevitable. Current treatment for recurrent glioblastoma (rGBM) is rapidly evolving, and emerging therapies aimed at targeting primary GBM are often first tested in rGBM to demonstrate safety and feasibility, which, in recent years, has primarily been in the form of immunotherapy.
The purpose of this review is to highlight progress in clinical trials of immunotherapy for rGBM, including immune checkpoint blockade, oncolytic virotherapy, chimeric antigen receptor (CAR) T-cell therapy, cancer vaccine and immunotoxins. Three independent reviewers covered literature, published between the years 2000 and 2022, in various online databases. In general, the efficacy of immunotherapy in rGBM remains uncertain, and is limited to subsets/small cohorts of patients, despite demonstrating feasibility in early-stage clinical trials.
However, considerable progress has been made in understanding the mechanisms that may preclude rGBM patients from responding to immunotherapy, as well as in developing new approaches/combination strategies that may inspire optimism for the utility of immunotherapy in this devastating disease. Continued trials are necessary to further assess the best therapeutic avenues and ascertain which treatments might benefit each patient individually.
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