Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, United States.
Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, United States.
Front Immunol. 2018 Oct 16;9:2380. doi: 10.3389/fimmu.2018.02380. eCollection 2018.
Patients with high risk neuroblastoma have a poor prognosis and survivors are often left with debilitating long term sequelae from treatment. Even after integration of anti-GD2 monoclonal antibody therapy into standard, upftont protocols, 5-year overall survival rates are only about 50%. The success of anti-GD2 therapy has proven that immunotherapy can be effective in neuroblastoma. Adoptive transfer of chimeric antigen receptor (CAR) T cells has the potential to build on this success. In early phase clinical trials, CAR T cell therapy for neuroblastoma has proven safe and feasible, but significant barriers to efficacy remain. These include lack of T cell persistence and potency, difficulty in target identification, and an immunosuppressive tumor microenvironment. With recent advances in CAR T cell engineering, many of these issues are being addressed in the laboratory. In this review, we summarize the clinical trials that have been completed or are underway for CAR T cell therapy in neuroblastoma, discuss the conclusions and open questions derived from these trials, and consider potential strategies to improve CAR T cell therapy for patients with neuroblastoma.
患有高危神经母细胞瘤的患者预后不良,幸存者往往因治疗而留下长期的衰弱后遗症。即使在将抗 GD2 单克隆抗体治疗纳入标准的 upfront 方案后,5 年总生存率仍仅约为 50%。抗 GD2 治疗的成功证明了免疫疗法在神经母细胞瘤中可能有效。嵌合抗原受体 (CAR) T 细胞的过继转移有可能在此基础上取得成功。在早期临床试验中,CAR T 细胞疗法治疗神经母细胞瘤已被证明是安全且可行的,但疗效仍存在显著障碍。这些障碍包括缺乏 T 细胞持久性和效力、难以确定靶点以及免疫抑制性肿瘤微环境。随着 CAR T 细胞工程的最新进展,许多实验室正在解决这些问题。在这篇综述中,我们总结了已完成或正在进行的神经母细胞瘤 CAR T 细胞治疗的临床试验,讨论了这些试验得出的结论和未解决的问题,并考虑了改善神经母细胞瘤患者 CAR T 细胞治疗的潜在策略。