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:Single center, real-world retrospective study of CAR-T cell therapy for relapsed/refractory large B-cell lymphoma beyond second line: five-year results at the University Hospitals Leuven.
Single center, real-world retrospective study of CAR-T cell therapy for relapsed/refractory large B-cell lymphoma beyond second line: five-year results at the University Hospitals Leuven.
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我们的真实世界数据显示缓解率高且持久,与 tisa-cel 相比,axi-cel 在疗效更高、毒性更高方面的趋势不具统计学显著性。
11 例患者(14%)未能接受 CAR-T 输注。在接受输注的患者(n = 68)中,tisa-cel 的最佳总缓解率(ORR)/完全缓解率(CR)为 64%/49%,axi-cel 为 88%/66%(ORR 比较 p = 0.04)。中位随访 13.8 个月后,tisa-cel 组 1 年无进展生存期(PFS)和总生存期(OS)分别为 30% 和 43%,axi-cel 组分别为 48% 和 62%。tisa-cel 后细胞因子释放综合征(CRS)总发生率/3 级发生率为 82%/9%,axi-cel 后为 97%/0%。tisa-cel 后免疫效应细胞相关神经毒性综合征(ICANS)总发生率/3 级发生率为 24%/18%,axi-cel 后为 54%/40%。输注队列非复发死亡率为 13%。
真实世界数据显示两种疗法均有较高且持久的应答,axi-cel 疗效和毒性较 tisa-cel 均较高,但差异趋势未达显著性。结果与其他真实世界登记数据一致,但中位 OS 较短且高级别 ICANS 较多。
Eleven patients (14%) did not proceed to CAR-T cell infusion. For infused patients ( n = 68), the best overall response rate (ORR)/complete response (CR) rate was 64%/49% for tisa-cel and 88%/66% for axi-cel ( p = 0.04 for ORR). After a median follow-up of 13.8 months, progression-free survival (PFS) and overall survival (OS) at 1 year were 30% and 43% for tisa-cel and 48% and 62% for axi-cel. Cytokine release syndrome (CRS) (all grades/grade 3) occurred in 82%/9% after tisa-cel and in 97%/0% after axi-cel. Immune effector cell-associated neurotoxicity syndrome (ICANS) (all grades/grade 3) occurred in 24%/18% after tisa-cel and in 54%/40% after axi-cel. The non-relapse mortality in the infusion cohort was 13%.
Our real-world data show high and durable response rates, with a non-significant trend towards a higher efficacy and higher toxicity for axi-cel compared to tisa-cel. Our results are in line with other real-world registries except for a shorter median OS and more high-grade ICANS.
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