Burns Ian, Gwynne William D, Suk Yujin, Custers Stefan, Chaudhry Iqra, Venugopal Chitra, Singh Sheila K
Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada.
Department of Surgery, McMaster University, Hamilton, ON, Canada.
Front Oncol. 2022 Jan 27;12:815726. doi: 10.3389/fonc.2022.815726. eCollection 2022.
Pediatric central nervous system (CNS) tumors are the most common solid tumors diagnosed in children and are the leading cause of pediatric cancer-related death. Those who do survive are faced with the long-term adverse effects of the current standard of care treatments of chemotherapy, radiation, and surgery. There is a pressing need for novel therapeutic strategies to treat pediatric CNS tumors more effectively while reducing toxicity - one of these novel modalities is chimeric antigen receptor (CAR) T-cell therapy. Currently approved for use in several hematological malignancies, there are promising pre-clinical and early clinical data that suggest CAR-T cells could transform the treatment of pediatric CNS tumors. There are, however, several challenges that must be overcome to develop safe and effective CAR T-cell therapies for CNS tumors. Herein, we detail these challenges, focusing on those unique to pediatric patients including antigen selection, tumor immunogenicity and toxicity. We also discuss our perspective on future avenues for CAR T-cell therapies and potential combinatorial treatment approaches.
小儿中枢神经系统(CNS)肿瘤是儿童期诊断出的最常见实体瘤,也是小儿癌症相关死亡的主要原因。那些存活下来的患儿面临着当前化疗、放疗和手术等标准治疗方法带来的长期不良影响。迫切需要新的治疗策略,以便更有效地治疗小儿CNS肿瘤,同时降低毒性——嵌合抗原受体(CAR)T细胞疗法就是这些新方法之一。目前已批准用于多种血液系统恶性肿瘤,有前景的临床前和早期临床数据表明,CAR-T细胞可能改变小儿CNS肿瘤的治疗方式。然而,要开发出用于CNS肿瘤的安全有效的CAR-T细胞疗法,必须克服几个挑战。在此,我们详细阐述这些挑战,重点关注小儿患者所特有的挑战,包括抗原选择、肿瘤免疫原性和毒性。我们还讨论了对CAR-T细胞疗法未来途径和潜在联合治疗方法的看法。