| Literature DB >> 33708205 |
Zhiling Yan1,2, Huanxin Zhang1,2, Jiang Cao1,2, Cheng Zhang3, Hui Liu4, Hongming Huang5, Hai Cheng1,2, Jianlin Qiao2, Ying Wang1,2, Yan Wang6, Lei Gao3, Ming Shi7,8,9, Wei Sang1,2, Feng Zhu1,2, Depeng Li1,2, Haiying Sun1,2, Qingyun Wu2, Yuekun Qi1,2, Hujun Li1,2, Xiangmin Wang1,2, Zhenyu Li1,2, Hong Liu6, Junnian Zheng7,8,9, Wenbin Qian4, Xi Zhang3, Kailin Xu1,2.
Abstract
Clinical trials have confirmed that chimeric antigen receptor (CAR) T cell therapies are revolutionizing approaches for treating several relapsed or refractory hematological tumors. Cytokine release syndrome (CRS) is an adverse event with high incidence during CAR-T treatment. A further understanding of the characteristics and related risk factors of CRS is important for effective management. A total of 142 patients with relapsed or refractory acute lymphocyte leukemia (ALL), lymphoma, or multiple myeloma (MM) received lymphodepletion chemotherapy followed by infusion of CAR-T cells. The characteristics of CRS at different time points after treatment were monitored and risk factors were analyzed. The incidence of CRS for ALL, lymphoma, and multiple myeloma were 82%, 90%, and 90% respectively. Fever was observed on a median of day 3 for ALL, day 1 for lymphoma, and day 8.5 for MM after CAR-T cell infusion, and the duration was different between grade 1-2 CRS and grade 3-5 CRS. Disease types, peak concentration of IL-6, and CRP were associated with CRS. For patients with ALL, numbers of lymphoblast in bone marrow before lymphodepletion, peak concentration of IL-6, and CRP were independent risk factors of CRS. Clinical stage of lymphoma patients and high tumor burden in marrow of MM patients were independent risk factors of CRS. In conclusion, the characteristics and risk factors of CRS in different B-cell hematological tumors are different and should be managed individually during CAR-T cell therapy.Entities:
Keywords: acute lymphocyte leukemia; chimeric antigen receptor T cell; cytokine release syndrome; lymphoma; multiple myeloma
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Year: 2021 PMID: 33708205 PMCID: PMC7940756 DOI: 10.3389/fimmu.2021.611366
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561