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依可卡替基因自体白细胞介素-2:首次获批。

Equecabtagene Autoleucel: First Approval.

作者信息

Keam Susan J

机构信息

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

出版信息

Mol Diagn Ther. 2023 Nov;27(6):781-787. doi: 10.1007/s40291-023-00673-y. Epub 2023 Sep 2.

Abstract

Equecabtagene autoleucel (Fucaso), an autologous anti-B cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR)-T cell therapy that uses lentivirus as a gene vector to transfect autologous T cells, is being developed by IASO Biotechnology and Innovent Biologics, Inc. for the treatment of multiple myeloma (MM) and autoimmune diseases of the nervous system, including neuromyelitis optica spectrum disorder (NMOSD). Equecabtagene autoleucel was granted conditional approval in China in June 2023 for the treatment of adults with relapsed or refractory MM (RRMM) who have progressed after ≥ 3 lines of therapy (≥ 1 proteasome inhibitor and an immunomodulator). This article summarizes the milestones in the development of equecabtagene autoleucel leading to this first approval in patients with RRMM who have progressed after multiple lines of therapy.

摘要

依可卡替基因自体白细胞介素(Fucaso)是一种自体抗B细胞成熟抗原(BCMA)导向的嵌合抗原受体(CAR)-T细胞疗法,它使用慢病毒作为基因载体转染自体T细胞,由IASO生物技术公司和信达生物制药集团股份有限公司联合开发,用于治疗多发性骨髓瘤(MM)和神经系统自身免疫性疾病,包括视神经脊髓炎谱系障碍(NMOSD)。依可卡替基因自体白细胞介素于2023年6月在中国获得有条件批准,用于治疗经过≥3线治疗(≥1种蛋白酶体抑制剂和1种免疫调节剂)后病情进展的复发或难治性成年MM(RRMM)患者。本文总结了依可卡替基因自体白细胞介素的研发历程中的重要节点,这些节点促成了其在多线治疗后病情进展的RRMM患者中的首次获批。

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