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阿加糖酶α注射用浓溶液:美国首次批准

Afamitresgene Autoleucel: First Approval.

机构信息

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

出版信息

Mol Diagn Ther. 2024 Nov;28(6):861-866. doi: 10.1007/s40291-024-00749-3. Epub 2024 Oct 15.

Abstract

Afamitresgene autoleucel (TECELRA), a genetically modified human leukocyte antigen (HLA)-restricted autologous melanoma-associated antigen 4 (MAGE-A4)-directed T cell immunotherapy, is being developed by Adaptimmune Therapeutics plc, for the treatment of solid tumours expressing the MAGE-A4 antigen. In August 2024, afamitresgene autoleucel was approved in the USA under accelerated approval for the treatment of adults with unresectable or metastatic synovial sarcoma who have received prior chemotherapy, are HLA-A02:01P, -A02:02P, -A02:03P or -A02:06P positive and whose tumour expresses the MAGE-A4 antigen as determined by FDA-approved or cleared companion diagnostic devices. This article summarizes the milestones in the development of afamitresgene autoleucel leading to this first approval for the treatment of advanced synovial sarcoma.

摘要

阿法美替基因自体细胞注射液(TECELRA)是一种经过基因修饰的人白细胞抗原(HLA)限制性自体黑色素瘤相关抗原 4(MAGE-A4)定向 T 细胞免疫疗法,由 Adaptimmune Therapeutics plc 开发,用于治疗表达 MAGE-A4 抗原的实体瘤。2024 年 8 月,阿法美替基因自体细胞注射液在美国获得加速批准,用于治疗先前接受过化疗、HLA-A02:01P、-A02:02P、-A02:03P 或 -A02:06P 阳性且肿瘤表达 MAGE-A4 抗原的不可切除或转移性滑膜肉瘤成人患者,该抗原的表达由 FDA 批准或清除的伴随诊断设备确定。本文总结了阿法美替基因自体细胞注射液开发过程中的重要里程碑,最终该药获得了首个用于治疗晚期滑膜肉瘤的批准。

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