Department of Oncology/Hematology, A.O.U. Città della Salute e della Scienza di Torino, Turin, Italy.
Department of Molecular Biotechnology and Health Sciences, University of Torino, Turin, Italy.
Front Immunol. 2020 May 12;11:888. doi: 10.3389/fimmu.2020.00888. eCollection 2020.
Research on CAR T cells has achieved enormous progress in recent years. After the impressive results obtained in relapsed and refractory B-cell acute lymphoblastic leukemia and aggressive B-cell lymphomas, two constructs, tisagenlecleucel and axicabtagene ciloleucel, were approved by FDA. The role of CAR T cells in the treatment of B-cell disorders, however, is rapidly evolving. Ongoing clinical trials aim at comparing CAR T cells with standard treatment options and at evaluating their efficacy earlier in the disease course. The use of CAR T cells is still limited by the risk of relevant toxicities, most commonly cytokine release syndrome and neurotoxicity, whose management has nonetheless significantly improved. Some patients do not respond or relapse after treatment, either because of poor CAR T-cell expansion, lack of anti-tumor effects or after the loss of the target antigen on tumor cells. Investigators are trying to overcome these hurdles in many ways: by testing constructs which target different and/or multiple antigens or by improving CAR T-cell structure with additional functions and synergistic molecules. Alternative cell sources including allogeneic products ( CAR T cells), NK cells, and T cells obtained from induced pluripotent stem cells are also considered. Several trials are exploring the curative potential of CAR T cells in other malignancies, and recent data on multiple myeloma and chronic lymphocytic leukemia are encouraging. Given the likely expansion of CAR T-cell indications and their wider availability over time, more and more highly specialized clinical centers, with dedicated clinical units, will be required. Overall, the costs of these cell therapies will also play a role in the sustainability of many health care systems. This review will focus on the major clinical trials of CAR T cells in B-cell malignancies, including those leading to the first FDA approvals, and on the new settings in which these constructs are being tested. Besides, the most promising approaches to improve CAR T-cell efficacy and early data on alternative cell sources will be reviewed. Finally, we will discuss the challenges and the opportunities that are emerging with the advent of CAR T cells into clinical routine.
嵌合抗原受体 T 细胞(CAR T 细胞)的研究近年来取得了巨大进展。在复发/难治性 B 细胞急性淋巴细胞白血病和侵袭性 B 细胞淋巴瘤中取得令人瞩目的结果后,两款 CAR T 产品,tisagenlecleucel 和 axicabtagene ciloleucel,先后获得 FDA 批准。然而,CAR T 细胞在 B 细胞疾病治疗中的作用正在迅速发展。正在进行的临床试验旨在比较 CAR T 细胞与标准治疗方案,并在疾病早期评估其疗效。CAR T 细胞的使用仍然受到相关毒性的限制,最常见的是细胞因子释放综合征和神经毒性,但这些毒性的管理已经有了显著改善。一些患者在治疗后没有反应或复发,要么是因为 CAR T 细胞扩增不佳,要么是因为缺乏抗肿瘤作用,要么是因为肿瘤细胞上靶抗原的丢失。研究人员正在尝试通过测试靶向不同和/或多个抗原的构建体,或通过用额外的功能和协同分子来改进 CAR T 细胞结构,以克服这些障碍。还考虑了替代细胞来源,包括同种异体产品(CAR T 细胞)、NK 细胞和诱导多能干细胞来源的 T 细胞。几项临床试验正在探索 CAR T 细胞在其他恶性肿瘤中的治疗潜力,最近多发性骨髓瘤和慢性淋巴细胞白血病的数据令人鼓舞。鉴于 CAR T 细胞适应证的可能扩展及其随着时间的推移更广泛的应用,需要越来越多的高度专业化的临床中心,配备专门的临床单位。总的来说,这些细胞疗法的成本也将在许多医疗保健系统的可持续性方面发挥作用。本综述将重点介绍 CAR T 细胞在 B 细胞恶性肿瘤中的主要临床试验,包括导致首次 FDA 批准的临床试验,以及正在测试这些构建体的新环境。此外,还将回顾提高 CAR T 细胞疗效的最有前途的方法和替代细胞来源的早期数据。最后,我们将讨论随着 CAR T 细胞进入临床常规带来的挑战和机遇。