帕纳替尼
嵌合抗原受体
医学
CD19
费城染色体
内科学
突变
Blinatumoab公司
抗原
肿瘤科
免疫学
T细胞
免疫系统
染色体易位
受体
生物
酪氨酸激酶
达沙替尼
遗传学
基因
作者
Fei Yang,Xiaodong Yang,Xiebing Bao,Liqing Kang,Lili Zhou,Xiaoxia Wu,Xiaowen Tang,Zhengzheng Fu,Xiao Ma,Aining Sun,Jian Zhang,Huiying Qiu,Deipei Wu
标识
DOI:10.1080/10428194.2019.1663417
摘要
Effective treatments for relapsed Ph+ALL with T315I mutation are few; CD19 CAR T-cell therapy are a potential therapy for this condition. We reported 7 patients with relapsed Ph+ALL with T315I mutation, who were treated pre- or post-allo-HSCT with CD19-specific CAR T-cells. Of the 7 cases, 6 were in CR or CRp within 1 month after the first infusion of CAR T-cells. MRD revealed a rapid decline in 6 patients. BCR/ABL fusion transcripts were negative in 4/5 cases (not performed in 2). Three patients maintained remission without evidence of MRD by QPCR until the final follow-up, of which 2 received anti-CD19 CAR T-cells and ponatinib at the same time. Our study confirmed the efficacy of anti-CD19 CAR T-cell therapy in treatment of relapsed Ph+ALL with T315I mutation pre- or post-allo-HSCT and the concurrent applicability of this therapy with ponatinib.
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