Vitale Candida, Strati Paolo
University Division of Hematology, A.O.U. Città della Salute e della Scienza di Torino and Department of Molecular Biotechnology and Health Sciences, University of Torino, Turin, Italy.
Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Front Oncol. 2020 May 27;10:849. doi: 10.3389/fonc.2020.00849. eCollection 2020.
Chimeric antigen receptor-modified (CAR) T cells targeting CD19 have revolutionized the treatment of relapsed or refractory aggressive B-cell lymphomas, and their use has increased the cure rate for these cancers from 10 to 40%. Two second-generation anti-CD19 CAR T-cell products, axicabtagene ciloleucel and tisagenlecleucel, have been approved for use in patients, and the approval of a third product, lisocabtagene maraleucel, is expected in 2020. The commercial availability of the first two products has facilitated the development of real-world experience in treating relapsed or refractory aggressive B-cell lymphomas, shed light on anti-CD19 CAR T-cell products' feasibility in trial-ineligible patients, and raised the need for strategies to mitigate the adverse effects associated with anti-CD19 CAR T-cell therapy, such as cytokine release syndrome, neurotoxicity, and cytopenia. In addition, promising clinical data supporting the use of anti-CD19 CAR T-cell therapy in patients with indolent B-cell lymphomas or chronic lymphocytic leukemia have recently become available, breaking the paradigm that these conditions are not curable. Multiple clinical CAR T-cell therapy-based trials are ongoing. These include studies comparing CAR T-cell therapy to autologous stem cell transplantation or investigating their use at earlier stages of disease, novel combinations, and novel constructs. Here we provide a thorough review on the use of the anti-CD19 CAR T-cell products axicabtagene ciloleucel, tisagenlecleucel and lisocabtagene maraleucel in patients with indolent or aggressive B-cell lymphoma or with chronic lymphocytic leukemia, and present novel CAR T cell-based approaches currently under investigation in these disease settings.
靶向CD19的嵌合抗原受体修饰(CAR)T细胞彻底改变了复发或难治性侵袭性B细胞淋巴瘤的治疗方式,其应用使这些癌症的治愈率从10%提高到了40%。两种第二代抗CD19 CAR T细胞产品,axi-cabtagene ciloleucel和tisagenlecleucel,已被批准用于患者,第三种产品lisocabtagene maraleucel预计在2020年获批。前两种产品的商业可用性促进了在治疗复发或难治性侵袭性B细胞淋巴瘤方面的真实世界经验的积累,阐明了抗CD19 CAR T细胞产品在不符合试验条件的患者中的可行性,并增加了对减轻与抗CD19 CAR T细胞疗法相关的不良反应(如细胞因子释放综合征、神经毒性和血细胞减少症)的策略的需求。此外,最近有支持在惰性B细胞淋巴瘤或慢性淋巴细胞白血病患者中使用抗CD19 CAR T细胞疗法的有前景的临床数据,打破了这些病症无法治愈的范式。多项基于CAR T细胞疗法的临床试验正在进行中。这些试验包括比较CAR T细胞疗法与自体干细胞移植的研究,或研究其在疾病早期阶段、新组合和新构建体中的应用。在此,我们全面综述了抗CD19 CAR T细胞产品axi-cabtagene ciloleucel、tisagenlecleucel和lisocabtagene maraleucel在惰性或侵袭性B细胞淋巴瘤或慢性淋巴细胞白血病患者中的应用,并介绍了目前在这些疾病背景下正在研究的基于CAR T细胞的新方法。