Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies

被引:88
作者
Liu, Jun [1 ]
Zhong, Jiang F. [2 ]
Zhang, Xi [1 ]
Zhang, Cheng [1 ]
机构
[1] Third Mil Med Univ, Xinqiao Hosp, Dept Hematol, Chongqing 400037, Peoples R China
[2] Univ Southern Calif, Herman Ostrow Sch Dent, Div Periodontol Diagnost Sci & Dent Hyg, Div Biomed Sci, Los Angeles, CA USA
基金
美国国家科学基金会;
关键词
CAR-T cells; Allogeneic hematopoietic stem cell transplantation; Lymphoid malignancies; CHIMERIC ANTIGEN RECEPTOR; ACUTE LYMPHOBLASTIC-LEUKEMIA; MINIMAL RESIDUAL DISEASE; DONOR LYMPHOCYTE INFUSION; CD19-TARGETED T-CELLS; VERSUS-HOST-DISEASE; BLINATUMOMAB; THERAPY; CHEMOTHERAPY; REMISSIONS;
D O I
10.1186/s13045-017-0405-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered the cornerstone in treatment of hematological malignancies. However, relapse of the hematological disease after allo-HSCT remains a challenge and is associated with poor long-term survival. Chimeric antigen receptor redirected T cells (CAR-T cells) can lead to disease remission in patients with relapsed/refractory hematological malignancies. However, the therapeutic window for infusion of CAR-T cells post allo-HSCT and its efficacy are debatable. Main body: In this review, we first discuss the use of CAR-T cells for relapsed cases after allo-HSCT. We then review the toxicities and the occurrence of graft-versus-host disease in relapsed patients who received CAR-T cells post allo-HSCT. Finally, we review clinical trial registrations and the therapeutic time window for infusion of CAR-T cells post allo-HSCT. Conclusions: The treatment of allogeneic CAR-T cells is beneficial for patients with relapsed B cell malignancies after allo-HSCT with low toxicities and complications. However, multicenter clinical trials with larger sample sizes should be performed to select the optimal therapeutic window and confirm its efficacy.
引用
收藏
页码:1 / 8
页数:8
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