2022 Chinese expert consensus and guidelines on clinical management of toxicity in anti-CD19 chimeric antigen receptor T-cell therapy for B-cell non-Hodgkin lymphoma

嵌合抗原受体 医学 细胞因子释放综合征 淋巴瘤 CD19 免疫疗法 B细胞 免疫学 T细胞 肿瘤科 Blinatumoab公司 抗原 癌症研究 内科学 癌症 免疫系统 抗体
作者
Ping Li,Yang Liu,Yun Liang,Jian Bo,Sujun Gao,Yongxian Hu,Yu Hu,He Huang,Xiao‐Jun Huang,Hongmei Jing,Xiaoyan Ke,Jianyong Li,Yuhua Li,Qifa Liu,Peihua Lu,Heng Mei,Ting Niu,Yongping Song,Yuqin Song,Liping Su
出处
期刊:Cancer biology and medicine [Chinese Anti-Cancer Association]
卷期号:20 (2): 129-146 被引量:17
标识
DOI:10.20892/j.issn.2095-3941.2022.0585
摘要

Adoptive cellular immunotherapy with chimeric antigen receptor (CAR) T cells has emerged as a novel modality for treating relapsed and/or refractory B-cell non-Hodgkin lymphoma (B-NHL). With increasing approval of CAR T-cell products and advances in CAR T cell therapy, CAR T cells are expected to be used in a growing number of cases. However, CAR T-cell-associated toxicities can be severe or even fatal, thus compromising the survival benefit from this therapy. Standardizing and studying the clinical management of these toxicities are imperative. In contrast to other hematological malignancies, such as acute lymphoblastic leukemia and multiple myeloma, anti-CD19 CAR T-cell-associated toxicities in B-NHL have several distinctive features, most notably local cytokine-release syndrome (CRS). However, previously published guidelines have provided few specific recommendations for the grading and management of toxicities associated with CAR T-cell treatment for B-NHL. Consequently, we developed this consensus for the prevention, recognition, and management of these toxicities, on the basis of published literature regarding the management of anti-CD19 CAR T-cell-associated toxicities and the clinical experience of multiple Chinese institutions. This consensus refines a grading system and classification of CRS in B-NHL and corresponding measures for CRS management, and delineates comprehensive principles and exploratory recommendations for managing anti-CD19 CAR T-cell-associated toxicities in addition to CRS.
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