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:Long-term follow-up of CD19 chimeric antigen receptor T cell therapy in acute lymphoblastic leukemia patients relapsed after allogeneic hematopoietic stem cell transplantation.
Long-term follow-up of CD19 chimeric antigen receptor T cell therapy in acute lymphoblastic leukemia patients relapsed after allogeneic hematopoietic stem cell transplantation.
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。
B-ALL患者在接受allo-HSCT后复发与不良预后相关。尽管CD19 CAR-T 细胞疗法在这一人群中显示出前景,但其长期疗效和安全性仍不明确。为解决这一问题,我们开展了一项回顾性多中心研究,评估自体与异体CD19 CAR-T 细胞疗法在55例allo-HSCT后复发的B-ALL患者中的长期生存结局。CAR-T 细胞输注后,37例患者(67.3%)达到CR。CR患者的3年无白血病生存率为37.8%。CR和未缓解患者的3年OS率为36.2%。细胞因子释放综合征是最常见的不良事件,发生于74.5%的患者中。自体与异体CAR-T 细胞组之间在疗效或安全性方面未发现显著差异(均P > 0.05)。
本研究表明,自体与异体CD19 CAR-T 细胞疗法均具有令人鼓舞的3年生存率和安全性特征,并进一步支持CD19 CAR-T 细胞疗法作为allo-HSCT后复发B-ALL患者的一种有价值的治疗选择。
Relapse after allogeneic hematopoietic stem cell transplantation (allo-HSCT) in patients with B-cell acute lymphoblastic leukemia (B-ALL) is associated with a poor prognosis. Although CD19 chimeric antigen receptor T (CAR-T) cell therapy has shown promise in this population, its long-term efficacy and safety remain unclear. To address this, we conducted a retrospective multicenter study to evaluate the long-term survival outcomes of autologous and allogeneic CD19 CAR-T cell therapies in 55 B-ALL patients who relapsed after allo-HSCT.
Following CAR-T cell infusion, 37 patients (67. 3%) achieved complete remission (CR). The 3-year leukemia-free survival rate among CR patients was 37. 8%. The 3-year overall survival rate for both CR and non-remission patients was 36. 2%. Cytokine release syndrome was the most common adverse event, occurring in 74. 5% of patients. No significant differences in efficacy or safety were found between autologous and allogeneic CAR-T cell groups (all P > 0. 05).
This study demonstrates the promising 3-year survival and safety profile of both autologous and allogeneic CD19 CAR-T cell therapies, and further supports CD19 CAR-T cell therapy as a valuable treatment for patients with relapsed B-ALL after allo-HSCT.
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