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:Case Report: Successful engraftment of allogeneic hematopoietic stem cells using CAR-T cell therapy as the conditioning regimen in R/R Ph(+) B cell acute lymphoblastic leukemia.
Case Report: Successful engraftment of allogeneic hematopoietic stem cells using CAR-T cell therapy as the conditioning regimen in R/R Ph(+) B cell acute lymphoblastic leukemia.
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我们报告了使用 CAR-T 细胞疗法作为 R/R B-ALL 患者预处理方案成功植入异基因 HSC。
在血液系统恶性肿瘤中,CAR-T 细胞治疗后进行巩固性异基因造血干细胞(allo-HSCs)移植是一种新兴的治疗模式。关于CAR-T 治疗后不进行预处理方案而直接进行异基因造血干细胞移植(allo-HSCT)成功与否的认识有限。病例介绍:我们报告一例复发/难治性(R/R)Ph+ B细胞急性淋巴细胞白血病(ALL)患者,接受了抗CD19 CAR-T 免疫治疗。治疗1个月后,骨髓增生仍然低下,造血功能无改善。据此,从HLA相合的同胞供者中提取异基因造血干细胞(HSCs),在CAR-T 细胞治疗后第33天输注给患者以支持造血。第40天,未成熟骨髓淋巴细胞水平为0%,微小残留病阴性,融合基因BCR/ABL 190阴性。嵌合体分析显示完全供者嵌合。CAR-T 细胞输注后3个月,患者仍处于完全缓解状态,伴完全供者嵌合。然而,观察到肝功能下降,伴有皮肤色素沉着和溃烂,提示急性移植物抗宿主病。由于经济原因,治疗中止。
Consolidative allogeneic hematopoietic stem cells (allo-HSCs) after chimeric antigen receptor T cells (CAR-T) therapy is an emerging modality in hematologic malignancies. Knowledge about the success of allogeneic hematopoietic stem cell transplantation (allo-HSCT) after CAR-T therapy without a conditioning regimen is limited. CASE PRESENTATION: We report a patient with relapsed/refractory (R/R) Ph + B-cell acute lymphoblastic leukemia (ALL) who underwent anti-CD19 CAR-T immunotherapy. After 1 month of treatment, bone marrow hyperplasia remained reduced with no hematopoietic improvements. In line with this, allogeneic hematopoietic stem cells (HSCs) were extracted from an HLA-matched sibling donor and administered to the patient on day 33 after CAR-T cell therapy to support hematopoiesis. On day 40, the level of immature bone marrow lymphocytes was at 0% and minimal residual disease-negative, and the fusion gene BCR/ABL 190 was negative. Chimerism analysis showed full donor chimerism. Three months after CAR-T cells infusion, the patient was still in complete remission with full donor chimerism. However, decreased liver function with skin pigmentation and festering, indicative of acute graft versus host disease, was noted. The treatment was halted owing to financial reasons.
We report the successful engraftment of allogeneic HSCs using CAR-T cell therapy as a conditioning regimen for R/R B-ALL patients.
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