Laura Samples, Hossein Sadrzadeh, Matthew J Frigault, Caron A Jacobson, Mehdi Hamadani, Ashwath Gurumurthi, Paolo Strati, Roni Shouval, Ariela Noy, Peter A Riedell, Saurabh Dahiya, David G Maloney, Brian G Till, Alexandre V Hirayama, Jordan Gauthier, Ajay K Gopal, Stephen D Smith, Christina Poh, Ryan Lynch, Chaitra Ujjani, Mengyang Di, Vikram Raghunathan, Mehrdad Shakib-Azar, Kikkeri N Naresh, Ted A Gooley, Jean Yared, Michael D Jain, Frederick L Locke, Lori Ann Leslie, Narendranath Epperla, Monalisa Ghosh, Alan Skarbnik, Brian T Hill, Manali K Kamdar, Valentin Ortiz-Maldonado, Nuria Martinez-Cibrian, Leyla Shune, Mazyar Shadman
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This multicenter, retrospective study evaluated real-world CD19 chimeric antigen receptor (CAR) T-cell therapy outcomes in patients with relapsed/refractory BL using data abstracted from the medical records. In total, 31 patients received CAR T cells after a median of 3 previous therapies (range, 1-6). Patients received axicabtagene ciloleucel (n = 19), lisocabtagene maraleucel (n = 4), tisagenlecleucel (n = 4), or other agents (n = 4). Grade 1 to 2 cytokine release syndrome occurred in 83.9% of patients (grade ≥3, 65%), and grade 1 to 2 immune effector cell-associated neurotoxicity syndrome (ICANS) occurred in 29% of patients (grade ≥3, 19.4%). The 28-day mortality rate was 16.1%, including 1 patient who died from grade 5 ICANS. The overall response rate at 1 month was 58.0% with a complete response (CR) rate of 41.9%; however, the 6-month CR rate was only 19.4%. The median progression-free survival was 2.3 months (95% confidence interval, 1.0-9.0), and the median overall survival was 6.0 months (95% confidence interval, 1.9-11.5). Three patients (9.7%) received consolidative allogeneic stem cell transplants, but all subsequently relapsed. In conclusion, CD19 CAR T-cell therapy infrequently delivers long-term disease control in BL. 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引用次数: 0
摘要
伯基特淋巴瘤(BL)是一种侵袭性b细胞淋巴瘤,复发/难治性疾病患者预后较差。这项多中心、回顾性研究使用从医疗记录中提取的数据,评估了复发/难治性BL患者的真实世界CD19 CAR - t细胞治疗结果。总共有31名患者接受了CAR - t细胞治疗,他们之前接受的治疗中位数为3次(范围1-6)。患者接受轴细胞(n = 19)、liso-cel (n = 4)、组织细胞(n = 4)或其他药物治疗(n = 4)。83.9%的患者发生1-2级CRS(分级≥3 6.5%),29%的患者发生1-2级ICANS(分级≥3 19.4%)。28天死亡率为16.1%,其中1例患者死于5级ICANS。1个月的总有效率为58.0%,完全缓解(CR)率为41.9%,而6个月的CR率仅为25.8%。中位无进展生存期为2.3个月(95% CI 1.0 - 9.0),中位总生存期为6.0个月(95% CI 1.9 - 11.5)。3例患者(9.7%)接受了巩固性异体干细胞移植,但随后均复发。总之,CD19 CAR - t细胞治疗很少能在BL中提供长期的疾病控制。需要进一步的研究来确定这些患者最有效的替代治疗方法。
Outcomes among adult recipients of CAR T-cell therapy for Burkitt lymphoma.
Abstract: Burkitt lymphoma (BL) is an aggressive B-cell lymphoma that is associated with poor outcomes in patients with relapsed/refractory disease. This multicenter, retrospective study evaluated real-world CD19 chimeric antigen receptor (CAR) T-cell therapy outcomes in patients with relapsed/refractory BL using data abstracted from the medical records. In total, 31 patients received CAR T cells after a median of 3 previous therapies (range, 1-6). Patients received axicabtagene ciloleucel (n = 19), lisocabtagene maraleucel (n = 4), tisagenlecleucel (n = 4), or other agents (n = 4). Grade 1 to 2 cytokine release syndrome occurred in 83.9% of patients (grade ≥3, 65%), and grade 1 to 2 immune effector cell-associated neurotoxicity syndrome (ICANS) occurred in 29% of patients (grade ≥3, 19.4%). The 28-day mortality rate was 16.1%, including 1 patient who died from grade 5 ICANS. The overall response rate at 1 month was 58.0% with a complete response (CR) rate of 41.9%; however, the 6-month CR rate was only 19.4%. The median progression-free survival was 2.3 months (95% confidence interval, 1.0-9.0), and the median overall survival was 6.0 months (95% confidence interval, 1.9-11.5). Three patients (9.7%) received consolidative allogeneic stem cell transplants, but all subsequently relapsed. In conclusion, CD19 CAR T-cell therapy infrequently delivers long-term disease control in BL. Further investigation is needed to determine the most effective alternative management strategy for these patients.
期刊介绍:
Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.