Department of Pediatrics, Bass Center for Childhood Cancer and Blood Disorders, Center for Cancer Cell Therapy, Stanford, USA.
Stanford Cancer Institute, Stanford University, Stanford, USA.
Expert Opin Biol Ther. 2020 May;20(5):503-516. doi: 10.1080/14712598.2020.1738378. Epub 2020 Mar 12.
: Chimeric antigen receptor (CAR) T cell therapy has provided patients with relapsed/refractory B cell malignancies a new therapeutic option, but this class of therapeutics has not demonstrated consistent therapeutic benefit in solid tumors.: Here we review the literature to identify numerous factors that contribute to this discrepancy, using pediatric cancers as a platform to understand these limitations. We discuss an inability to target highly and homogenously expressed lineage-associated antigens due to risks of on-target off-tumor toxicity, T cell dysfunction related to T cell exhaustion and the suppressive tumor microenvironment (TME), and inefficient CAR T cell trafficking into solid tumors. As our understanding of the biology of CAR T cells improves and innovations in engineering CAR platforms emerge, next generation CAR T cell therapeutics designed to overcome these challenges will enter the clinic for testing.: New approaches to address the challenges that have limited the efficacy of CAR T cell therapeutics in solid tumors are emerging. These approaches include next-generation CAR T cell engineering to overcome antigen heterogeneity, to mitigate T cell exhaustion and to prevent suppression by the TME, as well as novel approaches for regional delivery to facilitate tumor T cell trafficking.
嵌合抗原受体 (CAR) T 细胞疗法为复发/难治性 B 细胞恶性肿瘤患者提供了一种新的治疗选择,但这类疗法在实体瘤中并未显示出一致的治疗益处。在这里,我们回顾了文献,以确定导致这种差异的众多因素,并以儿科癌症为平台来了解这些局限性。我们讨论了由于靶向脱靶毒性风险而无法靶向高度和均匀表达的谱系相关抗原、与 T 细胞耗竭和抑制性肿瘤微环境 (TME) 相关的 T 细胞功能障碍,以及 CAR T 细胞向实体瘤的有效转移。随着我们对 CAR T 细胞生物学的理解不断提高,CAR 平台工程方面的创新不断涌现,旨在克服这些挑战的下一代 CAR T 细胞疗法将进入临床测试。为了解决限制 CAR T 细胞疗法在实体瘤中疗效的挑战,新的方法正在出现。这些方法包括下一代 CAR T 细胞工程,以克服抗原异质性、减轻 T 细胞耗竭和防止 TME 抑制,以及用于促进肿瘤 T 细胞迁移的新型区域递送方法。