肿瘤细胞治疗研究
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T-Cell Engagers Targeting BCMA, GPRC5D, or FcRH5 in Relapsed/Refractory Multiple Myeloma: The Landscape Beyond CAR-T Cell Therapy-A Systematic Review
Beyond Remission: Risk-Adapted Maintenance and Mechanism-Guided Salvage After CAR T-Cell Therapy for Multiple Myeloma.
对于持续性 MRD 阴性、无髓外疾病且免疫功能正在恢复的许多患者，结构化观察是合适的。持续性或升高的 MRD、残留病灶、侵袭性疾病生物学特征或不利的 CAR-T 细胞动力学，应促使尽早转介临床试验，而非自动进行慢性治疗。挽救治疗可能涉及 BCMA 再靶向、转换为 GPRC5D 或 FcRH5、常规减瘤、放疗、抗体-药物偶联物、双特异性抗体或第二种细胞平台。未来试验应评估无进展生存期，同时评估无感染生存期、无治疗间期、免疫恢复、生活质量以
Bispecific antibodies in the treatment of multiple myeloma.
Just scratching the surface: novel treatment approaches for multiple myeloma targeting cell membrane proteins.
Poor outcomes with BCMA-targeting bispecific antibodies following early relapse from ide-cel: a real-world French study.
Chimeric antigen receptor T cells targeting FcRH5 provide robust tumour-specific responses in murine xenograft models of multiple myeloma.
Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient?
Bispecific antibodies in multiple myeloma: maximizing potential through rational combination therapies.
Endless possibilities and how to exploit them? What is the optimal treatment sequence?
Emerging T-Cell Engagers and Novel Immunotargets in Multiple Myeloma.
在血液系统恶性肿瘤中，基于免疫的疗法表现出实质性且具有临床意义的活性，其结果因疾病亚型、靶抗原和治疗平台而异。在多发性骨髓瘤中，BCMA 导向的双特异性抗体，包括 teclistamab 和 elranatamab，在经过大量预处理的人群中分别实现了约 63% 和 61% 的总体缓解率 (ORR)，在关键研究中中位无进展生存期 (PFS) 约为 11 至 17 个月。MonumenTAL-1 研究 (NCT03399799) 中他克他单
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