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Focal radiation therapy combined with 4-1BB activation and CTLA-4 blockade yields long-term survival and a protective antigen-specific memory response in a murine glioma model.在小鼠胶质瘤模型中,局部放射治疗联合4-1BB激活和CTLA-4阻断可产生长期生存及保护性抗原特异性记忆反应。
PLoS One. 2014 Jul 11;9(7):e101764. doi: 10.1371/journal.pone.0101764. eCollection 2014.
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IL-2: the first effective immunotherapy for human cancer.白细胞介素-2:人类癌症的第一种有效免疫疗法。
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Heat-shock protein peptide complex-96 vaccination for recurrent glioblastoma: a phase II, single-arm trial.热休克蛋白肽复合物 96 疫苗治疗复发性胶质母细胞瘤:一项 II 期、单臂试验。
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Intratumoral IL-12 combined with CTLA-4 blockade elicits T cell-mediated glioma rejection.瘤内 IL-12 联合 CTLA-4 阻断引发 T 细胞介导的胶质细胞瘤排斥。
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Nivolumab plus ipilimumab in advanced melanoma.纳武利尤单抗联合伊匹单抗治疗晚期黑色素瘤。
N Engl J Med. 2013 Jul 11;369(2):122-33. doi: 10.1056/NEJMoa1302369. Epub 2013 Jun 2.
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Safety and tumor responses with lambrolizumab (anti-PD-1) in melanoma.拉罗替尼(anti-PD-1)治疗黑色素瘤的安全性和肿瘤应答。
N Engl J Med. 2013 Jul 11;369(2):134-44. doi: 10.1056/NEJMoa1305133. Epub 2013 Jun 2.
8
Ipilimumab alone or in combination with radiotherapy in metastatic castration-resistant prostate cancer: results from an open-label, multicenter phase I/II study.依匹单抗单药或联合放疗治疗转移性去势抵抗性前列腺癌:一项开放标签、多中心 I/II 期研究结果。
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9
IFNγ in combination with IL-7 enhances immunotherapy in two rat glioma models.IFNγ 与 IL-7 联合增强两种大鼠神经胶质瘤模型的免疫治疗。
J Neuroimmunol. 2013 May 15;258(1-2):91-5. doi: 10.1016/j.jneuroim.2013.02.017. Epub 2013 Mar 23.
10
Anti-PD-1 blockade and stereotactic radiation produce long-term survival in mice with intracranial gliomas.抗 PD-1 阻断和立体定向放疗可使颅内神经胶质瘤小鼠长期存活。
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胶质瘤的免疫治疗概念。

Concepts of immunotherapy for glioma.

作者信息

Patel Mira A, Pardoll Drew M

机构信息

Department of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.

出版信息

J Neurooncol. 2015 Jul;123(3):323-30. doi: 10.1007/s11060-015-1810-5. Epub 2015 Jun 13.

DOI:10.1007/s11060-015-1810-5
PMID:26070552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4498978/
Abstract

Immunotherapy is coming to the fore as a viable anti-cancer treatment modality, even in poorly immunogenic cancers such as glioblastoma (GBM). Accumulating evidence suggests that the central nervous system may not be impervious to tumor-specific immune cells and could be an adequate substrate for immunologic anti-cancer therapies. Recent advances in antigen-specific cancer vaccines and checkpoint blockade in GBM provide promise for future immunotherapy in glioma. As anti-GBM immunotherapeutics enter clinical trials, it is important to understand the interactions, if any, between immune-based treatment modalities and the current standard of care for GBM involving chemoradiation and steroid therapy. Current data suggests that chemoradiation may not preclude the success of immunotherapeutics, as their effects may be synergistic. The future of therapy for GBM lies in the power of combination modalities, involving immunotherapy and the current standard of care.

摘要

免疫疗法正作为一种可行的抗癌治疗方式崭露头角,即便在免疫原性较差的癌症如胶质母细胞瘤(GBM)中也是如此。越来越多的证据表明,中枢神经系统可能并非对肿瘤特异性免疫细胞毫无反应,并且可能是免疫抗癌疗法的合适作用底物。GBM中抗原特异性癌症疫苗和检查点阻断的最新进展为未来胶质瘤免疫疗法带来了希望。随着抗GBM免疫疗法进入临床试验,了解基于免疫的治疗方式与GBM当前的标准治疗(包括放化疗和类固醇治疗)之间的相互作用(如果存在的话)非常重要。目前的数据表明,放化疗可能并不妨碍免疫疗法取得成功,因为它们的效果可能具有协同作用。GBM治疗的未来在于联合治疗方式的力量,包括免疫疗法和当前的标准治疗。