多发性骨髓瘤患者接受 idecabtagene vicleucel 治疗后出现帕金森样迟发性神经毒性:临床病理、脑脊液及尸检分析
Parkinsonism-like delayed neurotoxicity after idecabtagene vicleucel therapy for multiple myeloma: clinicopathological, cerebrospinal fluid, and autop
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Parkinsonism-like delayed neurotoxicity after idecabtagene vicleucel therapy for multiple myeloma: clinicopathological, cerebrospinal fluid, and autop
JAK-STAT-activated, fratricide-resistant CAR-T cells targeting membrane-bound TNF effectively treat AML and solid tumors.
我们的研究强调 TNF-NTF 是一个有前景的细胞表面靶点,可用于 CAR-T 细胞疗法,不仅适用于 AML,也适用于实体瘤。
Elotuzumab enhances the anti-tumor activity of Vγ9Vδ2 T cells against primary effusion lymphoma.
我们的发现首次证明,Elo 可直接增强γδ T 细胞对 PEL 的抗肿瘤活性,为将 Elo 与γδ T 细胞疗法联合作为这种难治性淋巴瘤的潜在治疗策略提供了新的临床前证据。
Development and optimization of Eva1 (MPZL2) targeting chimeric antigen receptor T cells.
这些数据表明,人源化 Eva1CAR-T 在治疗多种 Eva1 阳性实体瘤方面具有有前景的治疗潜力。
Cost-effectiveness analysis of elranatamab versus physician's choice of treatment (non-BCMA-directed regimens) in patients with triple class exposed m
从医疗支付方角度来看,在基础案例和情景分析中,elranatamab 相较于 PCT 具有成本效益,其 ICER 始终低于日本通常接受的阈值;但鉴于非锚定 MAIC 和长期外推的不确定性,应谨慎解读这一结果。
Determinants of Efficacy and Optimization of Chimeric Antigen Receptor T-Cell Therapy for Treating Multiple Myeloma: Current Status and Future Perspec
嵌合抗原受体(CAR)T 细胞疗法已改变了复发/难治性多发性骨髓瘤(MM)的治疗格局,其中 BCMA 靶向产品在经多线治疗的患者中展现出前所未有的缓解率。
Reinforced antimyeloma therapy via dual-lymphoid activation mediated by a panel of antibodies armed with bridging-BiTE.
使用双特异性抗体(包括双特异性 T 细胞衔接器(BiTE))的免疫治疗有可能增强复发/难治性多发性骨髓瘤的治疗效果。
Flare of Pre-Existing Sarcoidosis After Anti-B-Cell Maturation Antigen CAR-T Therapy: Cutaneous Lesions Mimicking Extramedullary Myeloma Relapse.
Pre-CAR-HEMATOTOX at Leukapheresis Predicts Delayed Platelet Recovery After Idecabtagene Vicleucel in Multiple Myeloma.
在白细胞分离术时评估的 Pre-CAR-HEMATOTOX 可预测 ide-cel 后血小板恢复延迟,并可能支持 BT 选择前的早期风险分层。
Delayed-onset parkinsonism possibly associated with elranatamab treatment for relapsed/refractory multiple myeloma: a case report of a poorly characte
靶向 B 细胞成熟抗原(BCMA)的 T 细胞重定向疗法彻底改变了复发/难治性多发性骨髓瘤(MM)的治疗。
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