Ghilardi Guido, Paruzzo Luca, Patel Vrutti, Svoboda Jakub, Chong Emeline R, Fardella Eugenio, Chong Elise A, Gabrielli Giulia, Nasta Sunita D, Landsburg Daniel J, Carter Jordan, Pajarillo Raymone, Barta Stefan K, White Griffin, Weber Elizabeth, Napier Ellen, Porter David L, Garfall Alfred L, Schuster Stephen J, Ruella Marco
Lymphoma Program, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.
Center for Cellular Immunotherapies and Cellular Therapy and Transplant, University of Pennsylvania, Philadelphia, PA, USA.
J Hematol Oncol. 2024 Apr 22;17(1):19. doi: 10.1186/s13045-024-01542-9.
Bendamustine has been retrospectively shown to be an effective and safe lymphodepletion regimen prior to the anti-CD19 chimeric antigen receptor T cell (CART) products tisagenlecleucel and axicabtagene ciloleucel, as well as the anti-BCMA CART products idecabtagene vicleucel and ciltacabtagene autoleucel. However, bendamustine as lymphodepletion prior to lisocabtagene maraleucel (liso-cel), a 4-1BB co-stimulated, fixed CD4:CD8 ratio anti-CD19 CART product, has not been described yet. Thus, we studied a cohort of sequentially-treated patients with large B-cell lymphomas who received bendamustine lymphodepletion before liso-cel at the University of Pennsylvania between 5/2021 and 12/2023 (n = 31). Patients were evaluated for toxicities and responses. Of note, 7 patients (22.6%) would have dnot met the inclusion criteria for the registrational liso-cel clinical trials, mostly due to older age. Overall and complete response rates were 76.9% and 73.1%, respectively. At a median follow-up of 6.3 months, the 6-month progression-free and overall survival were 59.9% and 91.1%, respectively. Rates of cytokine-release syndrome (CRS) and neurotoxicity (ICANS) of any grade were 9.7% and 9.7%, respectively, with no grade ≥ 3 events. No infections were reported during the first 30 days following liso-cel infusion. Neutropenia ≥ grade 3 was observed in 29.0% of patients; thrombocytopenia ≥ grade 3 occurred in 9.7%. In conclusion, bendamustine lymphodepletion before liso-cel appears to be a strategy that can drive tumor responses while ensuring a mild toxicity profile.
回顾性研究表明,苯达莫司汀是一种有效且安全的淋巴细胞清除方案,可用于在使用抗CD19嵌合抗原受体T细胞(CART)产品替萨罗宁和阿基仑赛之前,以及在使用抗BCMA CART产品伊德凯达仑赛和西达基奥仑赛之前。然而,苯达莫司汀作为4-1BB共刺激、固定CD4:CD8比例的抗CD19 CART产品利司扑兰(liso-cel)之前的淋巴细胞清除剂,尚未见相关描述。因此,我们研究了一组在宾夕法尼亚大学于2021年5月至2023年12月期间接受利司扑兰治疗前接受苯达莫司汀淋巴细胞清除的大B细胞淋巴瘤序贯治疗患者(n = 31)。对患者进行毒性和反应评估。值得注意的是,7名患者(22.6%)不符合利司扑兰注册临床试验的纳入标准,主要原因是年龄较大。总体缓解率和完全缓解率分别为76.9%和73.1%。在中位随访6.3个月时,6个月无进展生存率和总生存率分别为59.9%和91.1%。任何级别的细胞因子释放综合征(CRS)和神经毒性(ICANS)发生率分别为9.7%和9.7%,无≥3级事件。利司扑兰输注后的前30天内未报告感染。29.0%的患者观察到≥3级中性粒细胞减少;9.7%的患者发生≥3级血小板减少。总之,利司扑兰之前使用苯达莫司汀进行淋巴细胞清除似乎是一种既能驱动肿瘤反应又能确保毒性较轻的策略。