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Bendamustine is safe and effective for lymphodepletion before tisagenlecleucel in patients with refractory or relapsed large B-cell lymphomas

氟达拉滨 医学 细胞因子释放综合征 苯达莫司汀 内科学 环磷酰胺 阿勒姆图祖马 美罗华 肿瘤科 免疫学 移植 化疗 淋巴瘤 嵌合抗原受体 免疫疗法 癌症
作者
Guido Ghilardi,Elise A. Chong,Jakub Svoboda,Philipp Wohlfarth,Sunita Nasta,Staci Williamson,J.D. Landsburg,James N. Gerson,Stefan K. Barta,Raymone Pajarillo,Jessie Myers,A.I. Chen,Levanto Schachter,Rebecca Yelton,Hatcher J. Ballard,Alexandria Hodges Dwinal,Shannon Gier,Danielle Victoriano,Elizabeth Weber,Ellen Napier,Alfred L. Garfall,David L. Porter,Ulrich Jäger,Richard T. Maziarz,Marco Ruella,Stephen J. Schuster
出处
期刊:Annals of Oncology [Elsevier]
卷期号:33 (9): 916-928 被引量:26
标识
DOI:10.1016/j.annonc.2022.05.521
摘要

Anti-CD19 chimeric antigen receptor T-cell immunotherapy (CAR-T) is now a standard treatment of relapsed or refractory B-cell non-Hodgkin lymphomas; however, a significant portion of patients do not respond to CAR-T and/or experience toxicities. Lymphodepleting chemotherapy is a critical component of CAR-T that enhances CAR-T-cell engraftment, expansion, cytotoxicity, and persistence. We hypothesized that the lymphodepletion regimen might affect the safety and efficacy of CAR-T.We compared the safety and efficacy of lymphodepletion using either fludarabine/cyclophosphamide (n = 42) or bendamustine (n = 90) before tisagenlecleucel in two cohorts of patients with relapsed or refractory large B-cell lymphomas treated consecutively at three academic institutions in the United States (University of Pennsylvania, n = 90; Oregon Health & Science University, n = 35) and Europe (University of Vienna, n = 7). Response was assessed using the Lugano 2014 criteria and toxicities were assessed by the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 and, when possible, the American Society for Transplantation and Cellular Therapy (ASTCT) consensus grading.Fludarabine/cyclophosphamide led to more profound lymphocytopenia after tisagenlecleucel infusion compared with bendamustine, although the efficacy of tisagenlecleucel was similar between the two groups. We observed significant differences, however, in the frequency and severity of adverse events. In particular, patients treated with bendamustine had lower rates of cytokine release syndrome and neurotoxicity. In addition, higher rates of hematological toxicities were observed in patients receiving fludarabine/cyclophosphamide. Bendamustine-treated patients had higher nadir neutrophil counts, hemoglobin levels, and platelet counts, as well as a shorter time to blood count recovery, and received fewer platelet and red cell transfusions. Fewer episodes of infection, neutropenic fever, and post-infusion hospitalization were observed in the bendamustine cohort compared with patients receiving fludarabine/cyclophosphamide.Bendamustine for lymphodepletion before tisagenlecleucel has efficacy similar to fludarabine/cyclophosphamide with reduced toxicities, including cytokine release syndrome, neurotoxicity, infectious and hematological toxicities, as well as reduced hospital utilization.

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