决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Tandem CD19/CD22 CAR T-cells as potential therapy for children and young adults with high-risk r/r B-ALL.
串联 anti-CD19/CD22 CAR T 细胞输注联合巩固性 HSCT 是一种有前景的治疗方法,但桥接治疗的管理以及输注前降低 TB 仍是关键挑战(REALL_CART 试验,NCT06709469,EudraCT 2023-509723-41-01)。
靶向 CD19 的嵌合抗原受体(CAR)T 细胞在难治/复发 B 细胞急性淋巴细胞白血病(r/r B-ALL)中显示出令人瞩目的疗效;然而,频繁复发要求采用多靶点策略。
我们报告了西班牙临床数据,关于以同情用药方式给予的串联抗CD19/CD22 CAR T细胞在一组10例重度经治的儿童、青少年和年轻成人(AYA)r/r B-ALL患者中的安全性和有效性。
大多数(9/10)患者为复发性 B-ALL,其中 7 例既往接受过抗 CD19 CAR T 细胞治疗,6 例接受过造血干细胞移植(HSCT)。2 例患者患有唐氏综合征。高级别 CRS/ICANS 增加以及促炎标志物(IL-6、LDH 和铁蛋白)升高与淋巴细胞清除前高肿瘤负荷(TB)的患者相关。输注后第 +28 天,8/10 例患者获得完全缓解(7 例为 MRD-),5/7 例患者在输注后三个月内接受 HSCT 作为巩固治疗。2 例在串联 anti-CD19/CD22 CAR 治疗后早期复发的患者接受了挽救治疗和 HSCT。在 18 个月随访时,总生存率(OS)为 70%(95% CI,47%-100%)。
BACKGROUND: Chimeric antigen receptor (CAR) T-cells targeting CD19 have shown impressive outcomes in refractory/relapsed B-cell acute lymphoblastic leukaemia (r/r B-ALL); however, frequent relapse demands multi-targeted approaches. METHODS: We report Spanish clinical data on the safety and efficacy of tandem anti-CD19/CD22 CAR T-cells administered on a compassionate use basis in a cohort of 10 heavily pretreated paediatric, adolescent, and young adult (AYA) patients with r/r B-ALL. FINDINGS: Most (9/10) of the patients had relapsed B-ALL, 7 having received previous anti-CD19 CAR T-cell therapy and 6 haematopoietic stem cell transplantation (HSCT). Two patients had Down syndrome. Increased high-grade CRS/ICANS and proinflammatory markers (IL-6, LDH and ferritin) correlated with patients with a high tumour burden (TB) before lymphodepletion. Complete remission on day +28 post-infusion was achieved in 8/10 patients (7 with MRD-), and 5/7 patients received HSCT as consolidative therapy within three months post-infusion. Two patients with early relapse after tandem anti-CD19/CD22 CAR received rescue therapy and HSCT. At the 18-month follow up, overall survival (OS) was 70% (95% CI, 47%-100%). INTERPRETATION: Tandem anti-CD19/CD22 CAR T-cell administration combined with consolidative HSCT is a promising therapeutic approach, though managing bridging therapy and reducing the TB prior to infusion remain key challenges (REALL_CART trial, NCT06709469, EudraCT 2023-509723-41-01). FUNDING: This work was supported by a grant from the Instituto de Salud Carlos III to APM PI22/01226, two grants from CRIS Cancer Foundation to Beat Cancer as part of the projects "Advanced Cell Therapy Unit Hospital Universitario La Paz" and JM "Proyecto Mateo: CAR T-cell therapy for juvenile myelomonocytic leukaemia" and "Terapia avanzada CAR-T CD19/CD22", Ayuda Nominativa de la Consejer a de Investigaci n, Comunidad de Madrid, Spain. Work in MI lab was funded by a grant from the Spanish Ministry of Science and Innovation (PID2020-114148RB-I00). VGG was granted with R o Hortega (AES 2022 exp. N . CM22/00078) and Juan Rod s (AES 2024 exp. N . JR24/00003) contracts from the Carlos III Health Institute (ISCIII) through the European Funds of the Recovery, Transformation and Resilience Plan and financed by the European Union NextGenerationEU.
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