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:Anti-CLL1-based CAR T-cells with 4-1-BB or CD28/CD27 stimulatory domains in treating childhood refractory/relapsed acute myeloid leukemia.
Anti-CLL1-based CAR T-cells with 4-1-BB or CD28/CD27 stimulatory domains in treating childhood refractory/relapsed acute myeloid leukemia.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
在治疗儿童复发/难治性急性髓系白血病中,含 4-1BB 或 CD28/CD27 共刺激元件的抗 CLL1 CAR-T 细胞观察到初步相似的疗效/安全性指标。
已有少量报告显示抗C型凝集素样分子1(CLL1)CAR-T 可治疗复发/难治性急性髓系白血病(R/R AML),但尚未比较不同共刺激结构域的影响。
初步比较研究纳入7名接受抗CLL1 CAR-T 的R/R AML儿童,其中4名接受CD28/CD27型CAR-T,3名接受4-1BB型CAR-T。
CD28/CD27组和4-1BB组总体缓解率分别为75%和66.7%。所有患者均发生1至2级CRS,仅1例出现2级ICANS。CAR-T 最长持续时间在CD28/CD27组为156天,在4-1BB组为274天。1年OS率为57.1%。
在治疗儿童R/R AML方面,抗CLL1 CAR-T 采用4-1BB或CD28/CD27共刺激结构域的初步疗效和安全性指标相近。
Though the efficacy of anti C-type lectin-like molecule-1 (CLL1) CAR T-cells in refractory/relapsed acute myeloid leukemia (R/R-AML) have been occasionally reported, the influence of co-stimulatory domain CAR T-cells is not investigated so far. METHOD: Seven R/R-AML children treated with anti-CLL1 CAR T-cells were enrolled onto this preliminary comparison study. Among these seven patients, four received CD28/CD27-based CAR T-cells therapy, and three received 4-1BB-based CAR T-cells therapy. RESULT: The overall response rates were 75% and 66.7% in CD28/CD27 and 4-1BB group respectively. All patients experienced grade 1 to 2 cytokine release syndrome, with only one patient experiencing grade 2 immune effector cell-associated neurotoxicity syndrome. The maximum CAR T-cells durations were 156 and 274 days for CD28/CD27 group and 4-1BB group respectively. The 1-yr overall survival rate was 57.1%.
A preliminary similar efficacy/safety index was observed in anti-CLL1-based CAR T-cells with 4-1BB or CD28/CD27 co-stimulatory elements in treating pediatric R/R-AML.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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