Neuro-Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA
Neuro-Oncology Branch, National Cancer Institute, Bethesda, Maryland, USA.
J Immunother Cancer. 2020 Feb;8(1). doi: 10.1136/jitc-2019-000379.
Immunomodulatory therapies targeting inhibitory checkpoint molecules have revolutionized the treatment of solid tumor malignancies. Concerns about whether systemic administration of an immune checkpoint inhibitor could impact primary brain tumors were answered with the observation of definitive responses in pediatric patients harboring hypermutated gliomas. Although initial clinical results in patients with glioblastoma (GBM) were disappointing, recently published results have demonstrated a potential survival benefit in patients with recurrent GBM treated with neoadjuvant programmed cell death protein 1 blockade. While these findings necessitate verification in subsequent studies, they support the possibility of achieving clinical meaningful immune responses in malignant primary brain tumors including GBM, a disease in dire need of additional therapeutic options. There are several challenges involved in treating glioma with immune checkpoint modulators including the immunosuppressive nature of GBM itself with high inhibitory checkpoint expression, the immunoselective blood brain barrier impairing the ability for peripheral lymphocytes to traffic to the tumor microenvironment and the high prevalence of corticosteroid use which suppress lymphocyte activation. However, by simultaneously targeting multiple costimulatory and inhibitory pathways, it may be possible to achieve an effective antitumoral immune response. To this end, there are now several novel agents targeting more recently uncovered "second generation" checkpoint molecules. Given the multiplicity of drugs being considered for combination regimens, an increased understanding of the mechanisms of action and resistance combined with more robust preclinical and early clinical testing will be needed to be able to adequately test these agents. This review summarizes our current understanding of T lymphocyte-modulating checkpoint molecules as it pertains to glioma with the hope for a renewed focus on the most promising therapeutic strategies.
靶向抑制性检查点分子的免疫调节疗法彻底改变了实体瘤恶性肿瘤的治疗方式。人们曾担心全身性给予免疫检查点抑制剂是否会影响原发性脑肿瘤,而儿童患有高度突变性神经胶质瘤时观察到明确的应答则回答了这个问题。尽管最初在胶质母细胞瘤(GBM)患者中的临床结果令人失望,但最近发表的结果表明,接受新辅助程序性细胞死亡蛋白 1 阻断治疗的复发性 GBM 患者有潜在的生存获益。虽然这些发现需要在后续研究中验证,但它们支持了在包括 GBM 在内的恶性原发性脑肿瘤中实现临床意义上的免疫反应的可能性,而 GBM 正是急需额外治疗选择的疾病。用免疫检查点调节剂治疗神经胶质瘤存在几个挑战,包括 GBM 本身具有高度抑制性检查点表达的免疫抑制性质、免疫选择性血脑屏障阻碍外周淋巴细胞向肿瘤微环境迁移的能力以及皮质类固醇的高使用率,皮质类固醇抑制淋巴细胞激活。然而,通过同时靶向多个共刺激和抑制途径,可能实现有效的抗肿瘤免疫反应。为此,现在有几种针对最近发现的“第二代”检查点分子的新型药物。鉴于正在考虑联合治疗方案的药物种类繁多,需要增加对作用机制和耐药性的理解,并结合更强大的临床前和早期临床试验,以便能够充分测试这些药物。本综述总结了我们目前对与神经胶质瘤相关的 T 淋巴细胞调节检查点分子的理解,希望重新关注最有前途的治疗策略。