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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Austrian Real-world Experience With Standard of Care Brexucabtagene Autoleucel in Patients With Relapsed or Refractory Mantle-Cell Lymphoma.
Austrian Real-world Experience With Standard of Care Brexucabtagene Autoleucel in Patients With Relapsed or Refractory Mantle-Cell Lymphoma.
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套细胞淋巴瘤(MCL)是一种罕见的B细胞恶性肿瘤,在复发/难治性(r/r)疾病情况下治疗形势严峻。Brexu-cel作为首个获批的CAR-T 细胞疗法,彻底改变了r/r MCL患者的治疗格局和结局。本回顾性研究分析了奥地利CAR-T 项目中入组的r/r MCL患者的真实世界数据。2021年至2025年1月期间,奥地利共分析了33例患者。纳入标准包括确诊为r/r MCL、年龄≥18岁以及确认入组CAR-T 项目。主要终点为总缓解率(ORR)、总生存期(OS)和无进展生存期(PFS)。其他终点包括CAR-T 特异性不良事件(AE)的发生率和严重程度,如细胞因子释放综合征(CRS)和免疫效应细胞相关神经毒性综合征(ICANS)。
在入组CAR-T 项目的全部33例患者中,24例(72.7%)接受了brexu-cel治疗,而9例(27.3%)接受了替代治疗。替代治疗最常见的原因是疾病进展。Brexu-cel的ORR为95.9%,2年OS率和PFS率分别为76.8%和50.8%。在替代治疗组中,2年OS率和PFS率分别为13.9%和18.5%。≥2级CRS和ICANS的发生率分别为62.5%和37.5%。未发生与brexu-cel相关的5级不良事件。在淋巴细胞清除时白细胞计数>4.1 G/L的患者中,≥2级CRS的发生率显著更高,而在淋巴细胞清除时中性粒细胞计数≥4.75 G/L与≥2级ICANS的发生率更高相关。
我们的研究首次提供了奥地利接受brexu-cel治疗的r/r MCL患者真实世界治疗轨迹和结局的见解。本分析证实,Brexu-cel在MCL中即使在真实世界背景下也具有高ORR和OS率。探索性分析提示,淋巴细胞清除时白细胞和中性粒细胞计数升高可能分别与CRS和ICANS风险增加相关。
Mantle-cell lymphoma (MCL) represents a rare B cell malignancy with a challenging treatment situation in the case of relapsed or refractory (r/r) disease. Brexu-cel as first approved chimeric antigen receptor T cell (CART) therapy revolutionized the therapeutic landscape and outcome in r/r MCL patients. This retrospective study analyzes the real-world data of patients with r/r MCL enrolled into the CART program in Austria.
In total, 33 patients in Austria were analyzed from 2021 to January 2025. Inclusion criteria comprised confirmed diagnosis of r/r MCL, an age ≥18 years and a confirmed enrollment into the CART program. Primary endpoints were the overall response rate (ORR), overall survival (OS) and progression-free survival (PFS).
Further endpoints included the incidence and severity of CART-specific adverse events (AE) such as the cytokine-release-syndrome (CRS) and the immune effector cell-associated neurotoxicity syndrome (ICANS). Of all 33 patients enrolled into the CART program, 24 patients (72. 7%) were treated with brexu-cel whereas 9 patients (27. 3%) received alternative treatments. Most common cause for alternative treatment was disease progression. The ORR for brexu-cel was 95. 9%, with a 2-year OS- and PFS rate of 76.
8% and 50. 8%, respectively. In the alternative treatment group, the 2-year OS and PFS rates were 13. 9% and 18. 5%. Grade ≥2 CRS and ICANS occurred in 62. 5% and 37. 5%, respectively. There were no Grade 5 adverse events related to brexu-cel. Patients with a leukocyte count >4. 1 G/L at the time point of lymphodepletion had a significantly higher incidence of CRS grade ≥2, whereas a neutrophil count ≥4. 75 G/L at the time point of lymphodepletion was associated with a higher incidence of ICANS grade ≥2.
Our study provides first insights into the real-world trajectories and outcomes of r/r MCL patients intended for brexu-cel treatment in Austria. This analysis confirms the high rates of ORR and OS of Brexu-cel in MCL also in the real-world setting. Exploratory analysis suggested that increased leukocyte and neutrophil counts at lymphodepletion may be associated with increased risk of CRS and ICANS, respectively.
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