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:Case Report: autologous stem cell boost enables hematopoietic recovery after severe cytopenia induced by BCMA-targeted bispecific antibody therapy in multiple myeloma.
Case Report: autologous stem cell boost enables hematopoietic recovery after severe cytopenia induced by BCMA-targeted bispecific antibody therapy in multiple myeloma.
Elranatamab 是一种靶向 B 细胞成熟抗原(BCMA)和 CD3 的双特异性抗体,在复发/难治性多发性骨髓瘤(RRMM)中显示出显著疗效。
Elranatamab是一种靶向B细胞成熟抗原(BCMA)和CD3的双特异性抗体,在复发或难治性多发性骨髓瘤(RRMM)中显示出显著疗效,但其治疗也存在血液学毒性风险。干细胞加量(SCB)是回输既往采集的自体CD34⁺造血干细胞,已被探索作为CAR-T 细胞治疗相关血细胞减少后的挽救策略;但其在双特异性抗体治疗后的作用尚不明确。我们报告一例59岁RRMM男性患者在接受elranatamab治疗后发生持续性全血细胞减少,并通过自体SCB成功挽救。患者于第+10天恢复中性粒细胞,于第+19天摆脱输血依赖,造血恢复后重新开始elranatamab治疗,未再出现严重血细胞减少。本病例显示,SCB可能有助于管理T细胞重定向疗法后的持续性血细胞减少,并支持尽早采集干细胞的重要性。
Elranatamab, a bispecific antibody targeting B-cell maturation antigen (BCMA) and CD3, has shown significant efficacy in relapsed or refractory multiple myeloma (RRMM). However, elranatamab therapy also carries a risk of hematologic toxicity. Stem cell boost (SCB), involving reinfusion of previously collected autologous CD34 + hematopoietic stem cells, has been explored as a salvage strategy after Chimeric Antigen Receptor T-cell (CAR T-cell) therapy-related cytopenias. To date, its role following bispecific antibody treatment remains unclear. We report the case of a 59-year-old man with RRMM who developed prolonged pancytopenia after elranatamab therapy, successfully rescued with autologous SCB. Neutrophil recovery occurred by day +10, transfusion independence by day +19, and hematologic recovery allowed elranatamab resumption without recurrence of severe cytopenia. This case demonstrates the potential utility of SCB for managing persistent cytopenias after T-cell-redirecting therapies and supports the importance of early stem cell collection.
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