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:Sequenced, Not Stirred: Positioning CAR T and Bispecific Antibody Therapy in Multiple Myeloma.
在本期《Blood Cancer Discovery》中,Merz及其同事研究了600多名接受CAR-T 细胞(CAR T)和/或双特异性抗体治疗的多发性骨髓瘤患者,重点关注序贯接受两种疗法的患者。
在本期《Blood Cancer Discovery》中,Merz及其同事研究了600多名多发性骨髓瘤患者,这些患者接受了CAR-T 细胞和/或双特异性抗体治疗;研究重点是先后接受这两种治疗的患者。研究发现,先采用CAR-T治疗可显著延长无进展生存期。值得注意的是,在先接受另一种治疗后疾病进展的患者中,两种治疗的结局相近,因此这一优势源于CAR-T治疗作为初始治疗时带来的获益。见Merz等人的相关文章,第697页。
In this issue of Blood Cancer Discovery, Merz and colleagues study more than 600 recipients of chimeric antigen receptor T-cell (CAR T) and/or bispecific antibody therapy in multiple myeloma with an emphasis on patients who received both modalities sequentially. They find a clear progression-free survival advantage when CAR T therapy was used first; importantly, because outcomes with both modalities were similar when following progression after the converse modality, this advantage was driven by CAR T therapy's up-front benefits. See related article by Merz et al, p. 697.
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