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替西卡宾泰(talicabtagene autoleucel):首次批准。

Talicabtagene Autoleucel: First Approval.

机构信息

Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.

出版信息

Mol Diagn Ther. 2024 Jul;28(4):495-499. doi: 10.1007/s40291-024-00719-9. Epub 2024 May 23.

Abstract

Talicabtagene autoleucel (NexCAR19™) is a chimeric antigen receptor (CAR) T-cell therapy being developed by the Indian Institute of Technology, Bombay (IIT-B) and Immunoadoptive Cell Therapy (ImmunoACT) for the treatment of relapsed/refractory B-cell malignancies. Talicabtagene autoleucel contains autologous T cells from the patient, which have been modified to express a humanized anti-CD19 CAR that targets B cells. A single intravenous dose of talicabtagene autoleucel was associated with high response rates in pooled results from a phase I and phase II trial in patients with relapsed/refractory B-cell malignancies. Talicabtagene autoleucel was approved in India for the treatment of relapsed/refractory B-cell lymphomas and relapsed/refractory B-cell acute lymphoblastic leukaemia on 13 October 2023. This article summarizes the milestones in the development of talicabtagene autoleucel leading to this first approval for relapsed/refractory B-cell lymphomas and relapsed/refractory B-cell acute lymphoblastic leukaemia.

摘要

替卡利尤单抗(NexCAR19)是一种嵌合抗原受体(CAR)T 细胞疗法,由印度理工学院孟买分校(IIT-B)和免疫过继细胞疗法(ImmunoACT)研发,用于治疗复发/难治性 B 细胞恶性肿瘤。替卡利尤单抗包含来自患者的自体 T 细胞,这些细胞经过修饰,表达了一种靶向 B 细胞的人源化抗 CD19 CAR。在复发/难治性 B 细胞恶性肿瘤的 I 期和 II 期临床试验的汇总结果中,单次静脉注射替卡利尤单抗与高反应率相关。替卡利尤单抗于 2023 年 10 月 13 日在印度获批用于治疗复发/难治性 B 细胞淋巴瘤和复发/难治性 B 细胞急性淋巴细胞白血病。本文总结了导致替卡利尤单抗首次获批用于治疗复发/难治性 B 细胞淋巴瘤和复发/难治性 B 细胞急性淋巴细胞白血病的研发里程碑。

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