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:Different treatment eras for relapsed and refractory primary mediastinal B-cell lymphoma patients: accessibility to CAR T cells is associated with a better prognosis in a pooled analysis of the REPRIME-FIL and the CART-SIE studies.
共纳入191例患者,其中87例接受CAR T细胞治疗,104例接受其他挽救治疗。
靶向CD19的嵌合抗原受体(CAR)T细胞疗法已证明作为复发/难治性(R/R)原发性纵隔B细胞淋巴瘤(PMBCL)患者的挽救治疗具有疗效,然而,此前尚未进行CAR T细胞活性与其他挽救治疗之间的直接比较。本研究旨在比较在不同时代接受治疗的R/R PMBCL患者的总生存期(OS),这些时代反映了2019年后R/R患者对CAR T细胞的可及性以及此前年份接受其他挽救方案治疗的情况。我们进行了一项汇总分析,纳入正在进行的多中心前瞻性观察性研究CART-SIE和回顾性REPRIME-FIL研究中所有受R/R PMBCL影响的患者。共纳入191例患者,87例接受CAR T细胞治疗,104例接受其他挽救治疗。
Chimeric Antigen Receptor (CAR) T-cell therapy targeting CD19 has demonstrated efficacy as salvage treatment for patients with relapsed/refractory (R/R) primary mediastinal B-cell lymphoma (PMBCL), however, a direct comparison between CAR T activity and other salvage treatments has not previously been performed. This study aims to compare overall survival (OS) in R/R PMBCL patients treated in different eras who reflect accessibility to CAR T-cells in R/R patient treated after 2019 and treatment with other salvage programs in the years before. We performed a pooled analysis including all pts affected by R/R PMBCL enrolled in the ongoing multicenter prospective observational study CART-SIE and in the retrospective REPRIME-FIL study. A total of 191 patients were included, 87 receiving CAR T cells and 104 treated with other salvage therapies. The 3-year OS from failure of first line treatment for the entire cohort was 62% (95% CI 55-69). The 6-months landmark analysis showed that patients treated with CAR T cells had a significantly reduced risk of death and a superior OS compared with those receiving other regimens (adjusted HR 0.34; 95%CI 0.17-0.66, p=0.001). Patients treated with CAR T cells also had superior OS compared with the subgroup of REPRIME patients who underwent ASCT (adjusted HR 0.27; 95%CI 0.13-0.66, p=0.001). Within the limitations inherent to a pooled analysis, administration of CAR T cells during salvage of R/R PMBCL patients appears to be associated with a longer OS with a risk of death approximately one-third of that observed in patients managed without CAR T.
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