Novel CAR T cell therapies for patients with large B cell lymphoma

被引:0
作者
Goto, Hideki [1 ]
Onozawa, Masahiro [2 ]
Teshima, Takanori [1 ,2 ]
机构
[1] Hokkaido Univ Hosp, Div Lab & Transfus Med, W7,N15,Kita Ku, Sapporo, Hokkaido, Japan
[2] Hokkaido Univ, Fac Med, Dept Hematol, Sapporo, Japan
关键词
CAR T; Chimeric antigen receptor; Tisagenlecleucel; Axicabtagene ciloleucel; Lisocabtagene maraleucel; MULTIPLE-MYELOMA; BISPECIFIC ANTIBODIES; TUMOR BURDEN; EFFICACY; LANDSCAPE;
D O I
10.1007/s12185-024-03792-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Approximately 60-70% of patients with large B cell lymphoma (LBCL) achieve long-term remission or a cure after initial treatment. However, patients who relapse or are refractory to initial treatment have a poor prognosis. Chimeric antigen receptor (CAR) T cell therapy has recently attracted attention for its potential to provide a cure or long-term remission even for LBCL that has relapsed or is refractory to conventional chemotherapy. Currently, three CAR T cell products are clinically available for LBCL: tisagenlecleucel (tisa-cel), axicabtagene ciloleucel (axi-cel) and lisocabtagene maraleucel (liso-cel). These CAR T cell products were initially approved as third- or later-line therapies worldwide. Recently, axi-cel and liso-cel have become feasible as second-line therapies for patients with early relapsed or refractory disease after first-line chemotherapy. Although a large body of data on CAR T cell therapy has been accumulated, the clinical question of how to choose between these three available CAR T cell products has yet to be resolved. The appropriate approach to treatment selection for patients who relapse after CAR T cell therapy also remains unclear. This review discusses treatment strategies to maximize the benefits of CAR T cell therapy.
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收藏
页码:6 / 14
页数:9
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