Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Daejeon 34141, Korea.
College of Pharmacy, Chungnam National University, Yuseong-gu, Daejeon 34134, Korea.
Int J Mol Sci. 2021 Nov 9;22(22):12126. doi: 10.3390/ijms222212126.
Cancer immunotherapy is becoming more important in the clinical setting, especially for cancers resistant to conventional chemotherapy, including targeted therapy. Chimeric antigen receptor (CAR)-T cell therapy, which uses patient's autologous T cells, combined with engineered T cell receptors, has shown remarkable results, with five US Food and Drug Administration (FDA) approvals to date. CAR-T cells have been very effective in hematologic malignancies, such as diffuse large B cell lymphoma (DLBCL), B cell acute lymphoblastic leukemia (B-ALL), and multiple myeloma (MM); however, its effectiveness in treating solid tumors has not been evaluated clearly. Therefore, many studies and clinical investigations are emerging to improve the CAR-T cell efficacy in solid tumors. The novel therapeutic approaches include modifying CARs in multiple ways or developing a combination therapy with immune checkpoint inhibitors and chemotherapies. In this review, we focus on the challenges and recent advancements in CAR-T cell therapy for solid tumors.
癌症免疫疗法在临床环境中变得越来越重要,特别是对于对传统化疗(包括靶向治疗)耐药的癌症。嵌合抗原受体 (CAR)-T 细胞疗法利用患者自身的 T 细胞,并结合工程化的 T 细胞受体,已取得显著成果,迄今为止已有 5 项美国食品和药物管理局 (FDA) 批准。CAR-T 细胞在血液恶性肿瘤中非常有效,例如弥漫性大 B 细胞淋巴瘤 (DLBCL)、B 细胞急性淋巴细胞白血病 (B-ALL) 和多发性骨髓瘤 (MM);然而,其在治疗实体瘤方面的疗效尚未得到明确评估。因此,许多研究和临床调查正在涌现,以提高 CAR-T 细胞在实体瘤中的疗效。新的治疗方法包括以多种方式修饰 CAR 或与免疫检查点抑制剂和化疗联合治疗。在这篇综述中,我们重点介绍了 CAR-T 细胞治疗实体瘤所面临的挑战和最新进展。
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