自体移植后 CD19/CD22 CAR-T 细胞鸡尾酒疗法是治疗复发/难治性中枢神经系统淋巴瘤的优化策略

Relapsed/refractory (R/R) primary and secondary central nervous system lymphomas (PCNSL, SCNSL) are associated with short survival and represent an unmet need, requiring novel effective strategies.

We retrospectively compared the safety and efficacy of CD19/22 CAR-T-cell therapy following ASCT (ASCT + CAR-T group), CD19/22 CAR-T-cell cocktail therapy (CAR-T group) and chemoimmunotherapy (CIT group) in treating R/R CNSL patients. Analysis of the differences in clinical characteristics among the three groups revealed that the median age in the CIT group was older than that in the ASCT + CAR-T group and CAR-T group, and the median number of prior lines of therapy in the CIT group was less than that in the other groups. Patients in the two CAR-T-therapy groups exhibited comparable incidences and severities of CRS and ICANS. Grade 4-5 CRS and ICANS were not observed in either CAR-T-cell therapy group.

The incidence of Grade 3/4 hematological toxicity in the ASCT + CAR-T and CAR-T groups was greater than that in the CIT group. The ORR was 82. 75% in the ASCT + CAR-T group, 60. 00% in the CAR-T group and 58. 83% in the CIT group. As of December 31, 2022, the median follow-up after therapy was 16. 73 months (range, 0. 67-42. 00 months). The median durations of PFS and OS were not reached in the ASCT + CAR-T group.

The median PFS in the CAR-T group was 4. 72 months, and OS was not reached. In the CIT group, the median PFS and OS were 6. 63 months and 16. 77 months, respectively. The 2-year PFS rate of patients in the ASCT + CAR-T group (65. 52%) was significantly greater than that of patients in the CAR-T group (30. 00%, P = 0. 0321) and CIT group (23. 53%, P = 0. 0043).

Our results support the development of CAR-T-cell therapy for R/R CNSL. With the durability of remission and low toxicity, ASCT combined with CAR-T-cell therapy appears to be a more effective and safer treatment option for primary and secondary R/R CNS lymphoma.