Savage William M, Yeary Mitchell D, Tang Anthony J, Sperring Colin P, Argenziano Michael G, Adapa Arjun R, Yoh Nina, Canoll Peter, Bruce Jeffrey N
Department of Neurological Surgery, Columbia University Irving Medical Center/NY-Presbyterian Hospital, New York, New York, USA.
Department of Pathology and Cell Biology, Columbia University Irving Medical Center/NY-Presbyterian Hospital, New York, New York, USA.
Neurooncol Pract. 2024 Apr 1;11(4):383-394. doi: 10.1093/nop/npae028. eCollection 2024 Aug.
Glioblastoma (GBM) is the most common primary brain cancer, comprising half of all malignant brain tumors. Patients with GBM have a poor prognosis, with a median survival of 14-15 months. Current therapies for GBM, including chemotherapy, radiotherapy, and surgical resection, remain inadequate. Novel therapies are required to extend patient survival. Although immunotherapy has shown promise in other cancers, including melanoma and non-small lung cancer, its efficacy in GBM has been limited to subsets of patients. Identifying biomarkers of immunotherapy response in GBM could help stratify patients, identify new therapeutic targets, and develop more effective treatments. This article reviews existing and emerging biomarkers of clinical response to immunotherapy in GBM. The scope of this review includes immune checkpoint inhibitor and antitumoral vaccination approaches, summarizing the variety of molecular, cellular, and computational methodologies that have been explored in the setting of anti-GBM immunotherapies.
胶质母细胞瘤(GBM)是最常见的原发性脑癌,占所有恶性脑肿瘤的一半。GBM患者预后较差,中位生存期为14至15个月。目前治疗GBM的方法,包括化疗、放疗和手术切除,仍然不够充分。需要新的治疗方法来延长患者生存期。尽管免疫疗法在其他癌症(包括黑色素瘤和非小细胞肺癌)中已显示出前景,但其在GBM中的疗效仅限于部分患者亚组。确定GBM中免疫疗法反应的生物标志物有助于对患者进行分层、识别新的治疗靶点并开发更有效的治疗方法。本文综述了GBM中免疫疗法临床反应的现有和新兴生物标志物。本综述的范围包括免疫检查点抑制剂和抗肿瘤疫苗接种方法,总结了在抗GBM免疫疗法背景下探索的各种分子、细胞和计算方法。