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:Bridging With Chimeric Antigen Receptor T-Cell Therapy or Chemotherapy to Allo-HSCT in B-ALL: A Comparison of Treatment Complications and Survival.
Bridging With Chimeric Antigen Receptor T-Cell Therapy or Chemotherapy to Allo-HSCT in B-ALL: A Comparison of Treatment Complications and Survival.
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我们的数据表明,在 B-ALL 患者中,CAR-T 细胞治疗与化疗后行 allo-HSCT 在大多数治疗相关并发症和生存方面相当。
对于B细胞急性淋巴细胞白血病(B-ALL)患者,CAR-T(CAR-T)细胞疗法或化疗达到完全缓解(CR)后再接受异基因造血干细胞移植(allo-HSCT),两者的安全性和疗效尚未得到充分比较。
我们比较了443例连续B-ALL患者的移植结局,其中50例通过CAR-T 治疗达到CR,393例通过化疗达到CR后接受allo-HSCT。中位随访时间为30个月(范围1–62个月)。
CAR-T 组慢性移植物抗宿主病发生率较低(30.9%比44.0%,P=0.020)。CAR-T 组肝静脉闭塞病发生率高于化疗组(4%比0.5%,P=0.003)。两组总生存率(90.9%比94.6%,P=0.158)和复发率(9.1%比8.4%,P=0.513)相近。然而,CAR-T 组移植后非复发死亡率较高(10.9%比4.3%,P=0.016),无白血病生存率较化疗组低(80.0%比86.8%,P=0.040)。
我们的数据表明,在B-ALL患者中,CAR-T 细胞疗法或化疗后再接受allo-HSCT,两组大多数治疗相关并发症和生存结局相近。
Comparisons of safety and efficacy of Allogeneic hematopoietic stem cell transplantation (allo-HSCT) following complete remission (CR) achieved by Chimeric antigen receptor T (CAR-T) cell therapy versus chemotherapy for B-cell acute lymphoblastic leukemia (B-ALL) have not been fully discussed.
We performed a comparison of transplant outcomes in 443 consecutive B-ALL patients who received allo-HSCT after achieving CR with CAR-T therapy (n = 50) or with chemotherapy (n = 393). The median follow-up time was 30 months (range: 1-62 months).
The CAR-T group had a lower incidence of chronic graft-versus-host disease (30.9% vs. 44.0%, p = 0.020). We also found that the incidence of veno-occlusive disease was higher in the CAR-T group compared to the chemotherapy group (4% vs. 0.5%; p = 0.003). The study revealed that both the CAR-T and chemotherapy groups exhibited comparable overall survival (90.9% vs. 94.6%, p = 0.158) and relapse incidences (9.1% vs. 8.4%, p = 0.513). However, incidences of non-relapse mortality after transplantation were higher in the CAR-T group (10.9% vs. 4.3%, p = 0.016), and leukemia-free survival was lower in the CAR-T group compared to the chemotherapy group (80.0% vs. 86.8%, p = 0.040).
Our data indicate that, in B-ALL patients, most treatment-related complications and survival were comparable between CAR T-cell therapy and chemotherapy followed by allo-HSCT.
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