Iqbal Madiha, Bansal Radhika, Yassine Farah, Gandhi Sangeetha, Rosenthal Allison, Moustafa Muhamad Alhaj, Li Zhuo, Craver Emily C, Mohty Razan, Murthy Hemant, Ayala Ernesto, Tun Han, Munoz Javier, Castro Januario, Lin Yi, Kharfan-Dabaja Mohamed A
Division of Hematology-Oncology and Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, Florida.
Division Hematology-Oncology and Blood and Marrow Transplantation Program, Mayo Clinic, Rochester, Minnesota.
Transplant Cell Ther. 2022 Oct;28(10):668.e1-668.e6. doi: 10.1016/j.jtct.2022.07.009. Epub 2022 Jul 14.
Chimeric antigen receptor (CAR) T cell therapy represents a significant advancement in the treatment of patients with relapsed/refractory B cell lymphoid malignancies. Cytokine release syndrome and immune effector cell-associated neurotoxicity represent the most acute serious adverse events post CAR T cell therapy but the occurrence and persistence of cytopenias post CAR T cell therapy represent a significant adverse event and a management challenge. While most patients typically recover blood counts by 30 days, a significant subset of patients have persistent or late cytopenias beyond 30 days. Patients receiving CAR T cell are heavily pre-treated and the impact of prior therapies on late cytopenias is not well understood. In this study, we found an association between increased number of rituximab infusions and/or cumulative rituximab dose received prior to CAR T cell infusion and persistent anemia and thrombocytopenia at 90 and 180 days afterwards. An overall increased number of prior lines of therapy was also associated with persistent lymphopenia and anemia at 90 days while receiving a prior autologous hematopoietic cell transplant was associated with a greater risk of neutropenia and lymphopenia.
嵌合抗原受体(CAR)T细胞疗法是复发/难治性B细胞淋巴瘤患者治疗中的一项重大进展。细胞因子释放综合征和免疫效应细胞相关神经毒性是CAR T细胞治疗后最严重的急性不良事件,但CAR T细胞治疗后血细胞减少的发生和持续存在是一个重大不良事件及管理挑战。虽然大多数患者通常在30天内恢复血细胞计数,但相当一部分患者在30天后仍有持续性或迟发性血细胞减少。接受CAR T细胞治疗的患者接受了大量的前期治疗,而先前治疗对迟发性血细胞减少的影响尚不清楚。在本研究中,我们发现CAR T细胞输注前利妥昔单抗输注次数增加和/或累积利妥昔单抗剂量与输注后90天和180天的持续性贫血和血小板减少之间存在关联。总体而言,先前治疗线数增加也与90天时的持续性淋巴细胞减少和贫血有关,而先前接受自体造血细胞移植则与中性粒细胞减少和淋巴细胞减少的风险增加有关。