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:Thiotepa and Busulfan Combined With Cyclophosphamide Conditioning Regimen Plus Maintenance Therapy Improved the Disease-Free Survival of Patients With Relapsed/Refractory Hematologic Malignancies After Undergoing Allogeneic Transplantation.
Thiotepa and Busulfan Combined With Cyclophosphamide Conditioning Regimen Plus Maintenance Therapy Improved the Disease-Free Survival of Patients With Relapsed/Refractory Hematologic Malignancies After Undergoing Allogeneic Transplantation.
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预处理方案对复发/难治性(R/R)恶性血液病患者至关重要。噻替哌是一种具有优异细胞毒性和血脑屏障通透性的烷化剂,已广泛用于淋巴瘤的预处理方案,近期也用于伴有中枢神经系统受累的急性白血病患者。本回顾性研究旨在观察由噻替哌、白消安和环磷酰胺(TBC)组成的预处理方案用于R/R血液病患者异基因造血干细胞移植(allo-HSCT)的疗效和安全性。2022年7月至2023年12月期间,共入选27例患者。中位随访时间为609(243-954)天,1年和估计2年总生存期(OS)率分别为85.2% 6.8%和76.5% 8.5%。1年和估计2年无病生存期(DFS)率分别为81.5% 7.5%和62.8% 12.2%。6例患者出现复发,1年和估计2年累积复发率(CIR)分别为14.8% 6.8%和31.0% 12.6%。2例患者死于移植物抗宿主病(GVHD)或感染。1年和估计2年非复发死亡率(NRM)分别为4.2% 4.1%和8.5% 5.8%。14例(51.9%)患者在allo-HSCT后接受了维持治疗。方案相关毒性大多耐受良好。多因素分析显示,HSCT前未达到首次完全缓解(CR1)和既往接受过CAR-T 细胞治疗是DFS不良的预测因素。
本研究表明,TBC预处理方案可能是接受allo-HSCT的R/R血液病患者的一种有前景的选择。
Conditioning regimens are critical for patients with relapsed/refractory (R/R) malignant hematologic diseases. Thiotepa, an alkylating agent with excellent cytotoxicity and blood brain barrier permeability, has been widely used in conditioning regimens for lymphoma and has recently been used in patients with acute leukemia with central nervous system involvement. The aim of this retrospective study was to observe the efficacy and safety of a conditioning regimen comprising thiotepa, busulfan, and cyclophosphamide (TBC) for allogeneic hematopoietic stem cell transplantation (allo-HSCT) in patients with R/R hematologic diseases. Between July 2022 and December 2023, 27 patients were selected. With a median follow-up of 609 (243-954) days, the 1-year and estimated 2-year overall survival (OS) rates were 85.
2% 6. 8% and 76. 5% 8. 5%, respectively. The 1-year and estimated 2-year disease-free survival (DFS) rates were 81. 5% 7. 5% and 62. 8% 12. 2%, respectively. Six patients experienced relapse, and the 1-year and estimated 2-year cumulative incidence of relapse (CIR) rates were 14. 8% 6. 8% and 31. 0% 12. 6%, respectively. Two patients died from graft-versus-host disease (GVHD) or infection.
The 1-year and estimated 2-year nonrelapse mortality (NRM) rates were 4. 2% 4. 1% and 8. 5% 5. 8%, respectively. 14 (51. 9%) patients received maintenance therapy after allo-HSCT. Regimen-related toxicities were mostly well tolerated. Multivariate analysis revealed that failure to achieve first complete remission (CR1) before HSCT and previous treatment with CAR-T cell were predictors of poor DFS.
This study suggests that the TBC conditioning regimen may be a promising option for patients with R/R hematologic diseases undergoing allo-HSCT.
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