Current Challenges in Chimeric Antigen Receptor T-cell Therapy in Patients With B-cell Lymphoid Malignancies

被引:6
作者
Kim, Seok Jin [1 ,2 ,3 ,4 ]
Yoon, Sang Eun [1 ,3 ]
Kim, Won Seog [1 ,3 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Hematol Oncol,Dept Med, Seoul, South Korea
[2] Sungkyunkwan Univ, Samsung Adv Inst Hlth Sci & Technol, Dept Hlth Sci & Technol, Sch Med, Seoul, South Korea
[3] Samsung Comprehens Canc Ctr, CAR T cell Therapy Ctr, Seoul, South Korea
[4] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Hematol Oncol,Dept Med, 81 Irwon Ro, Seoul 06351, South Korea
基金
新加坡国家研究基金会;
关键词
Key Words; Chimeric antigen receptor; Cytokine toxicity; Efficacy; Lymphoma; Multiple myeloma; CYTOKINE RELEASE SYNDROME; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; MANAGEMENT; NEUROTOXICITY; IMMUNOTHERAPY; TOXICITIES; ACTIVATION;
D O I
10.3343/alm.2023.0388
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Chimeric antigen receptor (CAR) T-cell therapy is a promising immunotherapy based on genetically engineered T cells derived from patients. The introduction of CAR T-cell therapy has changed the treatment paradigm of patients with B-cell lymphoid malignancies. However, challenging issues including managing life-threatening toxicities related to CAR T-cell infusion and resistance to CAR T-cell therapy, leading to progression or relapse, remain. This review summarizes the issues with currently approved CAR T-cell therapies for patients with relapsed or refractory B-cell lymphoid malignancies, including lymphoma and myeloma. We focus on unique toxicities after CAR T-cell therapy, such as cytokine-related events and hematological toxicities, and the mechanisms underlying post -CAR T-cell failure.
引用
收藏
页码:210 / 221
页数:12
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