[CAR T cell therapy in acute lymphoblastic leukemia].

Manik Chatterjee, Ralf C Bargou
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引用次数: 0

Abstract

Modern immunotherapy in the form of T‑cell-based CD19-targeted approaches, such as the approved bispecific T‑cell engager (BiTE antibody) blinatumomab and chimeric antigen receptor T cells (CAR T cells) with the approved products tisagenlecleucel and brexucabtagene autoleucel has revolutionized the treatment of B‑precursor acute lymphoblastic leukemia (ALL). The pivotal clinical trials for the approval, including follow-up studies as well as the now available real-world data outside of these trials, showed that CAR-T cell therapy provides an effective treatment option for patients with relapsed and refractory B‑precursor ALL after chemotherapy, improving an otherwise poor prognosis. In addition to the therapeutic response, side effects of CAR-T cell therapy and their clinical management are discussed. Furthermore, resistance mechanisms are discussed and an outlook on further development is given. The T‑precursor ALL remains a challenge due to its immunological complexity but new developments in CAR-T cell treatment approaches targeting CD5 and CD7 show that progress is also being made in this area.

CAR - T细胞治疗急性淋巴细胞白血病。
以T细胞为基础的cd19靶向方法的现代免疫疗法,如已批准的双特异性T细胞接触器(BiTE抗体)blinatumomab和嵌合抗原受体T细胞(CAR - T细胞)与已批准的产品tisagenlecleucel和brexucabtagene autoeucel,已经彻底改变了B前体急性淋巴细胞白血病(ALL)的治疗。该批准的关键临床试验,包括随访研究以及这些试验之外的现有真实数据,表明CAR-T细胞疗法为化疗后复发和难治性B前体ALL患者提供了有效的治疗选择,改善了预后不良的患者。除了治疗反应外,还讨论了CAR-T细胞治疗的副作用及其临床管理。讨论了耐药机理,并对今后的发展进行了展望。由于其免疫学复杂性,T前体ALL仍然是一个挑战,但靶向CD5和CD7的CAR-T细胞治疗方法的新发展表明,这一领域也正在取得进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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