Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Cancer Immunol Immunother. 2021 Aug;70(8):2379-2384. doi: 10.1007/s00262-021-02850-6. Epub 2021 Jan 18.
The treatment of refractory Burkitt's lymphoma (BL) is still a challenge. Although CAR-T cell therapy has achieved good responses in diffuse large B cell lymphoma, there is no case series report about the efficacy of CAR-T cell therapy in adult Burkitt's lymphoma. In this study, we evaluate the efficacy and safety of CAR19/22 T cell therapy in six refractory Burkitt's lymphoma cases with poor genetic prognostic factors. After CAR-T cell therapy, five cases had grade 1 and one had grade 3 cytokine release syndrome. Three patients achieved an objective response (3/6 50%), including two partial remission and one complete remission. One CR patient received allogeneic hematopoietic stem cell transplantation (HSCT) and one PR patient received CAR22/19-T cells following auto-HSCT, and they were still in remission at 37 and 22 months of follow-up, respectively. Interestingly, patients with bulky disease (case 2, 4 and 5) had higher levels of serum IL-2R, which was secreted by regulatory T cells, lower CAR lentiviral amplification and poorer prognosis with shorter survival time than cases with non-bulky disease. It is suggested that high tumor burden, more immune suppressive cells and limited CAR-T cell expansion might affect the efficacy of CAR-T cell therapy. CAR-T cell therapy in adult BL patients whose best response cannot achieve CR may need to bridge to other treatments (such as HSCT) early.
难治性伯基特淋巴瘤(BL)的治疗仍然是一个挑战。虽然 CAR-T 细胞疗法在弥漫性大 B 细胞淋巴瘤中已取得良好的反应,但尚无关于 CAR-T 细胞疗法在成人伯基特淋巴瘤中的疗效的病例系列报告。在这项研究中,我们评估了 CAR19/22 T 细胞疗法在 6 例具有不良遗传预后因素的难治性伯基特淋巴瘤中的疗效和安全性。在 CAR-T 细胞治疗后,5 例发生 1 级,1 例发生 3 级细胞因子释放综合征。3 例患者获得客观缓解(3/6,50%),包括 2 例部分缓解和 1 例完全缓解。1 例 CR 患者接受异基因造血干细胞移植(HSCT),1 例 PR 患者在自体 HSCT 后接受 CAR22/19-T 细胞治疗,随访 37 个月和 22 个月时仍处于缓解状态。有趣的是,肿块较大的患者(病例 2、4 和 5)具有更高水平的血清 IL-2R,这是由调节性 T 细胞分泌的,CAR 慢病毒扩增较低,预后较差,生存时间较短。这表明高肿瘤负荷、更多的免疫抑制细胞和有限的 CAR-T 细胞扩增可能会影响 CAR-T 细胞疗法的疗效。对于最佳反应不能达到完全缓解的成人 BL 患者,CAR-T 细胞治疗可能需要尽早桥接到其他治疗(如 HSCT)。