作者
Xinfeng Chen,Xin Li,Yanfen Liu,Zhen Zhang,Shouxin Zhang,Jianmin Huang,Hong Li,Feng Li,Lei Zhang,Ling Li,Xiaolong Wu,Wang Ma,Zhenchang Sun,Hui Yu,Zhi-Yuan Zhou,Xiaoyan Feng,Kang Cui,Zhaoming Li,Hongling Zhang,Ying Zeng,Xiaochun Wan,Youhai H. Chen,Mingzhi Zhang,Yi Zhang
摘要
Aim: CD19 chimeric antigen receptor (CAR) T cells have been approved by the US FDA for treatment of relapsed and refractory (R/R) B-cell malignancies. Patients & methods: This study investigated the safety and efficacy of autologous 4-1BB costimulatory domain-engineered CD19 CAR-T cells in R/R B-cell lymphoma. Results: After CD19 CAR-T-cell infusion, severe cytokine release syndrome occurred in 28.6% (4/14) of the patients. The overall response rate was 77% with complete remission observed in 6/14 patients at 3 months. A higher tumor burden and grade 3-4 of myelosuppression after chemotherapy were associated with severe cytokine-release syndrome. Notably, combining CD19 CAR-T cells and PD-1 blockade, but not CD19 CAR-T cells alone, reduced intracranial tumor burden in a patient with central invasion of lymphoma. Conclusion: CD19 CAR-T cells could effectively induce tumor remission and PD-1 blockade might improve the efficacy in Chinese patients with R/R B-cell lymphoma.