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: Different outcomes of two cases of relapsed/refractory T cell acute lymphoblastic leukemia treated with anti-CD7 chimeric antigen receptor T cells bridging to allogeneic hematopoietic stem cell transplantation: from curative promise to fatal risk.
Case report: Different outcomes of two cases of relapsed/refractory T cell acute lymphoblastic leukemia treated with anti-CD7 chimeric antigen receptor T cells bridging to allogeneic hematopoietic stem cell transplantation: from curative promise to fatal risk.
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CAR-T 细胞治疗后进行巩固性异基因造血干细胞移植(allo-HSCT)是血液系统恶性肿瘤的新兴治疗方式,但CAR-T 与allo-HSCT之间的最佳间隔和预处理方案尚缺乏充分认识。本文报告两例确诊复发/难治性(R/R)T细胞急性淋巴细胞白血病(T-ALL)患者,先接受自体抗CD7 CAR-T 输注作为桥接,再接受allo-HSCT。病例1预后不佳,出现3级细胞因子释放综合征(CRS)、感染、药物相关器官毒性、超急性移植物抗宿主病(GVHD)及移植相关血栓性微血管病(TA-TMA)。相较之下,病例2病程较好,表现为炎症控制有效、CAR-T 治疗后完全康复并及时接受移植。这两例提示抗CD7 CAR-T 是治疗R/R T-ALL的有前景策略,但与allo-HSCT整合属于高危临床方案,需要谨慎且个体化管理。
Consolidative allogeneic hematopoietic stem cell transplantation (allo-HSCT) after chimeric antigen receptor (CAR) T-cell therapy is an emerging modality in hematologic malignancies. Knowledge regarding the optimal interval and pretreatment regimen between CAR T-cell therapy and allo-HSCT remains limited.
Here, we report two cases of confirmed relapsed/refractory (R/R) T-cell acute lymphoblastic leukemia (T-ALL) treated with autologous anti-CD7 CAR T cells infusion bridging to allo-HSCT. Case 1 had a poor prognosis due to grade 3 cytokine release syndrome (CRS), infection, drug-related organ toxicity, hyperacute graft-versus-host disease (GVHD), and transplant-associated thrombotic microangiopathy (TA-TMA).
In contrast, case 2 demonstrated a favorable course, marked by effective inflammation control, complete recovery following CAR T-cell therapy, and timely transplantation. These cases indicate that anti-CD7 CAR T-cell therapy represents a promising therapeutic strategy for R/R T-ALL.
However, its integration with allo-HSCT constitutes a high-risk clinical approach that requires careful and individualized management.
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