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