| Literature DB >> 33813229 |
Xiaoqian Liu1, Yuanfeng Zhang1, Kaimin Li1, Yinghui Liu1, Junqing Xu1, Junjie Ma1, Licai An1, Hui Wang1, Xiaoxia Chu2.
Abstract
Refractory/relapsed B cell lymphoma patients who received the available anti-CD19 chimeric antigen receptor (CAR) T cells may still experience a short duration of remission. Here in this study, we evaluated the safety and efficacy of a novel dominant-negative programmed cell death-1 (PD-1) armored anti-CD19 CAR T cells. A total of 9 patients (including 4 diffuse large B cell lymphomas, DLBCL, 2 transformed follicular lymphomas, TFL, and 3 follicular lymphomas, FL) received the novel CAR T cells infusion at a dose of more than 1 × 106/kg. Grade ≥ 3 cytokine release syndrome (CRS) and neurotoxicity were observed in 11.1% (n = 1/9) and 11.1% (n = 1/9) of patients, respectively. The overall response rate (ORR) was 77.8% (n = 7/9) and complete response (CR) rate was 55.6% (n = 5/9). Two patients have ongoing CR (all at 20+ months). CAR T cells expanded after infusion and continued to be detectable at 12+ months in patients with ongoing CR. This novel CD19-CAR T cell was safe and effective with durable remissions in patients with refractory/relapsed B cell lymphoma.Entities:
Keywords: Chimeric antigen receptor T cell (CAR T cell); Clinical trial; Lymphoma; Programmed cell death-1(PD-1)
Year: 2021 PMID: 33813229 DOI: 10.1016/j.tranon.2021.101085
Source DB: PubMed Journal: Transl Oncol ISSN: 1936-5233 Impact factor: 4.243