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:Prognostic Significance of Cytokine Release Syndrome in B Cell Hematological Malignancies Patients After Chimeric Antigen Receptor T Cell Therapy.
Prognostic Significance of Cytokine Release Syndrome in B Cell Hematological Malignancies Patients After Chimeric Antigen Receptor T Cell Therapy.
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细胞因子释放综合征(CRS)是嵌合抗原受体(CAR)T细胞治疗最常见的靶向毒性。然而,CRS的预后意义尚未得到充分阐明。我们研究的目的是在一个包含22例复发/难治性B细胞血液系统恶性肿瘤患者的回顾性队列中,评估抗CD19 CAR-T 治疗后CRS与疗效之间的关联。CAR-T 治疗后的完全缓解(CR)率为68%,无进展生存期(PFS)的中位值为6.8个月。22例患者中有8例(36.4%)表现为2级CRS。统计分析发现,2级CRS患者的CR率高于<2级CRS患者,PFS也更长。此外,桥接造血干细胞移植是PFS的另一项独立预测因素。这些数据提示,适当的CRS可能有利于CAR-T 治疗的疗效。临床试验注册号为NCT03110640、NCT03302403。
Cytokine release syndrome (CRS) is the most common on-target toxicity of chimeric antigen receptor (CAR) T cell therapy.
However, the prognostic significance of CRS has not been well elucidated. The aim of our study was to evaluate the association between CRS and efficacy after anti-CD19 CAR-T therapy in a retrospective cohort of 22 patients with relapsed/refractory B cell hematological malignancies.
The complete remission (CR) rates after CAR-T therapy were 68%, and median value for progression-free survival (PFS) was 6. 8 months. Eight of 22 (36. 4%) patients showed grade 2 CRS. Statistical analysis found that patients with grade 2 CRS had higher CR rates and longer PFS than those with < grade 2 CRS.
Moreover, bridging hematopoietic stem cell transplantation was another independent predictor for PFS. These data suggested that appropriate CRS may be beneficial to the efficacy of CAR-T therapy. The Clinical Trial Registration number is NCT03110640, NCT03302403.
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