Effective anti-BCMA retreatment in multiple myeloma

被引:33
|
作者
Gazeau, Nicolas [1 ]
Beauvais, David [1 ]
Yakoub-Agha, Ibrahim [1 ,2 ]
Mitra, Suman [3 ,4 ]
Campbell, Timothy B. [5 ]
Facon, Thierry [1 ]
Manier, Salomon [1 ,3 ,4 ]
机构
[1] Lille Univ, Dept Hematol, CHU Lille, Lille, France
[2] Lille Univ, INSERM, Infinite, U1286, Lille, France
[3] Lille Univ, Canther, INSERM, UMR S1277, Lille, France
[4] Lille Univ, CNRS, UMR9020, Lille, France
[5] Bristol Myers Squibb, Princeton, NJ USA
关键词
BAFF; APRIL;
D O I
10.1182/bloodadvances.2021004176
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The recent emergence of anti-B-cell maturation antigen (BCMA) therapies holds great promise in multiple myeloma (MM). These include chimeric antigen receptor (CAR) T cells, bispecific antibodies, and antibody-drug conjugates. Their development in clinical trials and further approval are changing the strategy for treating MM. Considering that a cure has not been reached, a central question in the coming years will be the possibility of using these therapies sequentially. Here, we report 2 cases of the serial use of anti-BCMA therapies with parallel monitoring of BCMA expression and anti-CAR antibodies. We further discuss recent data from clinical studies that have informed us about the different mechanisms of resistance to anti-BCMA therapies, including antigen escape, BCMA shedding, anti-drug antibodies, T-cell exhaustion, and the emergence of an immunosup-pressive microenvironment. This knowledge will be essential to help guide the strategy of serial treatments with anti-BCMA therapies.
引用
收藏
页码:3016 / 3020
页数:5
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