Xue Fei, Liu Rui, Fu Zhonghua, Zheng Peihao, Yang Fan, Feng Shaomei, Guo Yuelu, Shi Hui, Ma Lixia, Deng Biping, Ke Xiaoyan, Hu Kai
Department of Lymphoma and Myeloma Research Center, Beijing Gobroad Boren Hospital, Beijing, China.
Cytology Laboratory, Beijing Gobroad Boren Hospital, Beijing, China.
Cytotherapy. 2025 Aug;27(8):910-916. doi: 10.1016/j.jcyt.2025.04.063. Epub 2025 Apr 17.
Loss or mutation of antigen and limited chimeric antigen receptor (CAR) T-cell persistence in vivo are essential determinants of recurrence in relapsed/refractory diffuse large B-cell lymphoma (r/r DLBCL). Sequential infusion of CD19 and CD20 CAR Tcells (sequential CD19-20 CAR T-cell therapy) have been proposed as a potential solution. From March 2019 to January 2022 in Beijing Gobroad Boren Hospital, a total of 21 patients with r/r DLBCL received the CD19-20 CAR T-cell therapy in the prospective study (Clinical Trials Number: ChiCTR1900020980).Grade ≥3 cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were observed in 9.5% (2/21) and 0% (0/21) of patients, respectively. The CD20 CAR T-cell infusion did not increase severe toxicity. There were no treatment-related deaths. Of 21 patients, 13 (61.9%) attained partial responses (PRs) and 8 (38.1%) attained complete responses (CRs) within 90 days after CD19 CAR T-cell infusion. Subsequent treatment with CD20 CAR T-cell infusion resulted in 10 of the 13 initial PR patients converting to CR, with a median time to achieving CR of 30 days (range, 30-90). With a median follow-up of 24.7 months (range, 11.6-45.86), 71.4% (15/21) of patients maintained ongoing responses at the data cutoff date. Overall, sequential CD19-CD20 CAR T-cell therapy demonstrated a favorable safety profile and might enhance long-term clinical outcomes.