CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Robust CAR T-cell expansion and superior outcomes in DLBCL patients in complete response at infusion.
Robust CAR T-cell expansion and superior outcomes in DLBCL patients in complete response at infusion.
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历来认为,存在可测量病灶是刺激CAR-T 细胞扩增和持久性的必要条件。然而,输注前已达到完全缓解(CR)的患者中,CAR-T 细胞动力学仍知之甚少。
本研究旨在评估按输注前疾病状态分层的复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)患者结局及CAR-T 细胞动力学。在这项单中心回顾性分析中,纳入87例患者,其中23例(26.4%)CAR-T 细胞输注前处于CR,64例(73.6%)未达到CR。CR患者的无进展生存期(PFS)和总生存期均显著优于未达CR患者。外周血CAR-T 细胞动力学指标,包括CAR-T 细胞、CD4+ CAR-T 细胞和CD8+ CAR-T 细胞的比例及绝对计数,CR组与非CR组之间均无显著差异。无论CAR-T 细胞产品基于4-1BB还是CD28,这些发现均一致。
此外,对通过PET-CT达到完全代谢缓解(CMR)患者的分析证实,CMR与非CMR患者的CAR-T 细胞扩增和持久性相近。
我们的发现表明,即使没有可测量病灶,CAR-T 细胞疗法仍能使CR患者获得强劲扩增和良好生存结局。
Historically, the presence of measurable disease has been considered essential to stimulate CAR T-cell expansion and persistence.
However, the kinetics of CAR T cells in patients achieving complete response (CR) before infusion remain poorly understood.
This study aimed to evaluate the outcomes and CAR T-cell kinetics in relapsed/refractory diffuse large B-cell lymphoma (DLBCL) patients stratified by pre-infusion disease status. In this retrospective analysis of 87 patients treated at a single institution, 23 (26. 4%) were in CR and 64 (73. 6%) were in non-CR prior to CAR T-cell infusion.
Patients in CR exhibited significantly better progression-free survival (PFS) and overall survival compared to non-CR patients. Peripheral blood CAR T-cell kinetics, including the proportion and absolute counts of CAR T cells, CD4+ CAR T cells and CD8+ CART cells, showed no significant differences between CR and non-CR groups.
These findings were consistent across different CAR T-cell products, whether 4-1BB- or CD28-based.
Moreover, an analysis of patients achieving complete metabolic response (CMR) by PET-CT confirmed comparable CAR T-cell expansion and persistence in both CMR and non-CMR patients.
Our findings demonstrate that CAR T-cell therapy achieves robust expansion and favourable survival outcomes in CR patients, even in the absence of measurable disease.
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