Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY 14642, USA.
Future Oncol. 2021 Apr;17(11):1269-1283. doi: 10.2217/fon-2020-0291. Epub 2021 Jan 15.
Axicabtagene ciloleucel and brexucabtagene autoleucel are anti-CD19 T-cell therapies that utilize the same second-generation chimeric antigen receptor with a CD28 costimulatory subunit. They have demonstrated high rates of response in high-risk patients with relapsed and refractory B-cell malignancies in multicenter clinical trials, including diffuse large B-cell and mantle cell lymphomas. The high clinical activity has led to the US FDA approval of axicabtagene ciloleucel for diffuse large B-cell lymphoma, and brexucabtagene autoleucel for mantle cell lymphoma. While they are highly effective, they have significant toxicities, including cytokine release syndrome and neurologic toxicities, which can be severe and require specialized management. This review will discuss the development, efficacy and safety of axicabtagene ciloleucel and brexucabtagene autoleucel in B-cell lymphomas.
阿基仑赛和瑞基仑赛都是抗 CD19 T 细胞疗法,利用相同的第二代嵌合抗原受体,带有 CD28 共刺激亚基。在包括弥漫性大 B 细胞淋巴瘤和套细胞淋巴瘤在内的多中心临床试验中,它们在复发/难治性 B 细胞恶性肿瘤的高危患者中表现出了高缓解率。高临床活性导致美国 FDA 批准阿基仑赛用于弥漫性大 B 细胞淋巴瘤,批准瑞基仑赛用于套细胞淋巴瘤。虽然它们非常有效,但也有显著的毒性,包括细胞因子释放综合征和神经毒性,这些毒性可能很严重,需要专门的管理。这篇综述将讨论阿基仑赛和瑞基仑赛在 B 细胞淋巴瘤中的开发、疗效和安全性。