决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Elranatamab: First Approval.
Elranatamab(elranatamab-bcmm;ELREXFIO™)是一种由辉瑞公司开发的靶向BCMA的双特异性CD3 T细胞衔接器,用于治疗多发性骨髓瘤(MM)。
Elranatamab(elranatamab-bcmm;ELREXFIO™)是一种由辉瑞公司开发的双特异性B细胞成熟抗原(BCMA)导向的CD3 T细胞衔接器,用于治疗多发性骨髓瘤(MM)。Elranatamab将T细胞上的CD3与多发性骨髓瘤细胞上表达的BCMA桥接,从而激活T细胞,诱导T细胞介导的对骨髓瘤细胞的细胞毒性。2023年8月,elranatamab在美国获得首次批准,用于治疗既往接受过至少四线治疗(包括蛋白酶体抑制剂、免疫调节剂和抗CD38单克隆抗体)的复发或难治性多发性骨髓瘤(RRMM)成人患者。Elranatamab基于缓解率和缓解持久性获得该适应症的加速批准,持续批准可能取决于确证性试验中临床获益的证明。Elranatamab在欧盟也获得了针对RRMM的积极意见,目前正在日本和全球其他几个国家接受监管审查。Elranatamab的临床研究也正在世界各国进行。本文总结了elranatamab开发过程中的里程碑事件,这些事件促成了其首次获批用于治疗RRMM。
Elranatamab (elranatamab-bcmm; ELREXFIO™) is a bispecific B-cell maturation antigen (BCMA)-directed CD3 T cell engager being developed by Pfizer for the treatment of multiple myeloma (MM). Elranatamab bridges CD3 on T cells with BCMA expressed on multiple myeloma cells, thereby activating T cells to induce T cell-mediated cytotoxicity against myeloma cells. In August 2023, elranatamab received its first approval in the USA for the treatment of adult patients with relapsed or refractory multiple myeloma (RRMM) who have received at least four prior lines of therapy including a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 monoclonal antibody. Elranatamab received accelerated approval for this indication based on response rate and durability of response, and continued approval may be contingent on the demonstration of clinical benefit in a confirmatory trial(s). Elranatamab has also received a positive opinion in the EU for RRMM and is under regulatory review in Japan and several other countries worldwide. Clinical studies of elranatamab are also underway in countries around the world. This article summarizes the milestones in the development of elranatamab leading to this first approval for the treatment of RRMM.
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