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:Routine Monitoring of CAR-T-Cells Expansion and Persistence in Patients With Aggressive Large B-Cell Lymphoma by Flow Cytometry: A Single-Center Experience.
Routine Monitoring of CAR-T-Cells Expansion and Persistence in Patients With Aggressive Large B-Cell Lymphoma by Flow Cytometry: A Single-Center Experience.
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这项回顾性单中心研究评估了45例侵袭性大B细胞淋巴瘤(LBCL)患者中常规流式细胞术(FC)监测CAR-T 细胞的应用。研究评估了第0天至第12个月CAR-T 细胞扩增情况。阿基仑赛(axi-cel)治疗后第7天达到扩增峰值(占总淋巴细胞中位数39.3%;87个细胞/mm³),替沙仑赛(tisa-cel)治疗后第10天达到峰值(中位数8.1%;33.2个细胞/mm³)。CAR-T 细胞扩增较多与免疫相关毒性有关:2级细胞因子释放综合征(CRS)患者的CAR-T 峰值中位水平为52.8%,无CRS患者为6.6%(P<.001);发生免疫效应细胞相关神经毒性综合征(ICANS)的患者为60.8%,未发生者为15.3%(P<.001)。65%的患者出现长期血细胞减少,且在CAR-T 扩增较多者中更常见。
本研究表明,FC是常规临床实践中监测CAR-T 细胞动态的实用工具,有望用于早期毒性风险评估和个体化支持治疗。
This retrospective, single-center study evaluated routine flow cytometry (FC) monitoring of CAR-T-cells in 45 patients with aggressive large B-cell lymphoma (LBCL). CAR-T-cells expansion was assessed from Day 0 to Month 12. Peak expansion occurred on Day 7 after axi-cel (median 39. 3% of total lymphocytes; 87 cells/mm 3 ) and Day 10 for tisa-cel (median 8. 1%; 33. 2 cells/mm 3 ).
Greater CAR-T-cells expansion was associated with immune-related toxicity, with median peak levels reaching 52. 8% in patients with grade 2 cytokine release syndrome (CRS) versus 6. 6% in those without (p < 0. 001) and 60. 8% in patients with immune effector cell-associated neurotoxicity syndrome (ICANS) versus 15. 3% in those without (p < 0. 001). Prolonged cytopenia was observed in 65% of patients and more frequently among those with greater CAR-T-cells expansion.
This study highlights FC as a practical tool for monitoring CAR-T-cells dynamics in routine practice, with potential implications for early toxicity risk assessment and personalized supportive care.
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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