细胞因子释放综合征
硼替佐米
细胞因子
癌症研究
单克隆抗体
CD8型
多发性骨髓瘤
抗体
等离子体电池
T细胞
沙利度胺
单克隆
医学
来那度胺
CD3型
临床研究阶段
耐火材料(行星科学)
蛋白酶体抑制剂
浆细胞骨髓瘤
淋巴瘤
肿瘤科
内科学
浆细胞白血病
细胞毒性
免疫疗法
美罗华
自体干细胞移植
免疫系统
细胞毒性T细胞
进行性疾病
泊马度胺
白血病
免疫球蛋白G
药理学
化疗
无进展生存期
免疫学
作者
Peter T. Tan,Li Bao,Qingsong Yin,Chunrui Li,Sorab Jehangir Shavaksha,Henry Miles Prince,Zhen Cai,Shan Gao,Qian Wang,Di Wang,Yi Li,M. Zhang,Qiumei Deng,Qiaoyang Lu,Chengjun Jiang,Fang Ren,Danqing Wu,Shuqi Zeng,Yonghong Zhu,Tao Yi
摘要
To the Editor, Relapsed or refractory multiple myeloma (MM) remains a challenging disease to treat despite the introduction of immunomodulatory drugs (IMiDs), proteasome inhibitors (PIs), and anti-CD38 monoclonal antibodies (mAbs) which have substantially improved patient survival [1]. BCMA (B cell maturation antigen)—with high expression in plasmablasts (PBs) and mature plasma cells (PCs)—has emerged as a key therapeutic target in MM. In heavily pretreated patients with RRMM, BCMA-targeted CAR-T and bispecific TCEs therapies [2, 3] have demonstrated objective response rates (ORR) ranging from 61% to 97%. However, these treatments are associated with a high overall incidence of cytokine release syndrome (CRS) at 66.7%–94.8%, and immune effector cell-associated neurotoxicity syndrome (ICANS) at rates of 3%–18%.
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