儿童脑肿瘤的免疫治疗:考虑、挑战和未来方向

S. Eline, V. Jasper, Hulleman Esther
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摘要

中枢神经系统(CNS)肿瘤是儿童癌症相关死亡的主要原因。虽然在过去的几十年里,各种儿童癌症的存活率有所提高,但儿童脑肿瘤的治疗进展甚微。此外,目前的传统治疗方法会产生严重的长期毒性,因此迫切需要开发新的治疗方法。免疫疗法在成人实体瘤和儿童血液肿瘤中都是成功的,并且可能是儿童中枢神经系统恶性肿瘤的一种选择。然而,儿童脑肿瘤具有很强的免疫抑制微环境,这被认为是有效免疫治疗的主要障碍。这些肿瘤的低突变负担可能会进一步影响对该患者群体的免疫治疗。然而,直接将当前的免疫调节疗法直接应用于肿瘤的可能性,为这一人群的免疫治疗开辟了新的选择。本文综述了免疫治疗方法,包括免疫检查点抑制、嵌合抗原受体T (CAR-T)细胞治疗、治疗性癌症疫苗和溶瘤病毒治疗。我们回顾了它们对免疫抑制肿瘤微环境的影响,总结了目前的试验,并讨论了未来的发展方向。我们得出结论,免疫疗法对患有中枢神经系统恶性肿瘤的儿童有希望,特别是当与不同的(免疫)治疗策略相结合时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunotherapy in pediatric brain tumors: considerations, challenges and future directions
Tumors of the central nervous system (CNS) are the main cause of cancer-related death in children. While improvements in survival rates for various childhood cancers have been obtained over the last decades, little progress has been made for pediatric brain tumors. In addition, current conventional treatment gives rise to severe long term toxicity, which underpins the burning need for the development of novel therapeutic modalities. Immunotherapy was shown to be successful in both adult solid tumors and pediatric hemato-oncology, and may be an option for pediatric CNS malignancies. However, pediatric brain tumors have a strong immunosuppressive microenvironment, which is considered a major hurdle for effective immunotherapy. The low mutational burden of these tumors may compromise immunotherapy for this patient group even further. The possibility to directly apply the current immune modulating therapies directly into the tumor, however, opens new options for immunotherapy in this population. This review covers immunotherapeutic approaches including immune checkpoint inhibition, chimeric antigen receptor T (CAR-T) cell therapy, therapeutic cancer vaccines, and oncolytic virotherapy. We review their effect on the immunosuppressive tumor microenvironment, summarize current trials, and discuss future directions. We conclude that immunotherapy holds promise for children with CNS malignancies, especially when combined with different (immune) therapeutic strategies.
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