Department of Neurological Surgery, University of California, San Francisco, San Francisco, California.
The Parker Institute for Cancer Immunotherapy, San Francisco, California.
Clin Cancer Res. 2018 Nov 1;24(21):5198-5205. doi: 10.1158/1078-0432.CCR-17-2769. Epub 2018 Jun 5.
The field of cancer immunotherapy has made exciting progress for some cancer types in recent years. However, recent failures of late-phase clinical trials evaluating checkpoint blockade in patients with glioblastoma (GBM) represent continued challenges for brain cancer immunotherapy. This is likely due to multiple factors including but not limited to marked genetic and antigenic heterogeneity, relatively low mutational loads, and paucity of GBM-infiltrating T cells. We review recent and ongoing studies targeting the checkpoint molecules as monotherapy or in combination with other modalities, and discuss the mechanisms underlying the unresponsiveness of GBM to single-modality immunotherapy approaches. We also discuss other novel immunotherapy approaches that may promote T-cell responses and overcome the "cold tumor" status of GBM, including oncolytic viruses and adoptive T-cell therapy. .
近年来,癌症免疫疗法在一些癌症类型方面取得了令人兴奋的进展。然而,最近评估检查点阻断在胶质母细胞瘤(GBM)患者中的后期临床试验的失败,代表着脑癌免疫疗法仍面临持续的挑战。这可能是由于多种因素造成的,包括但不限于明显的遗传和抗原异质性、相对较低的突变负荷以及浸润性 T 细胞的缺乏。我们综述了近期和正在进行的针对检查点分子的单药或联合其他方式的研究,并讨论了 GBM 对单模态免疫治疗方法无反应的机制。我们还讨论了其他可能促进 T 细胞反应并克服 GBM 的“冷肿瘤”状态的新型免疫治疗方法,包括溶瘤病毒和过继性 T 细胞疗法。