Immunotherapeutic and Targeted Approaches in Multiple Myeloma

被引:17
|
作者
Nadeem, Omar [1 ]
Tai, Yu-Tzu [1 ]
Anderson, Kenneth C. [1 ]
机构
[1] Harvard Med Sch, Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
关键词
immunotherapy multiple myeloma; chimeric antigen receptor T-cell therapy; CAR T-cell therapy; bispecific antibodies; immunomodulatory agents; IMID; monoclonal antibodies; MoAB; STEM-CELL TRANSPLANTATION; LOW-DOSE DEXAMETHASONE; TERM-FOLLOW-UP; MATURATION ANTIGEN; OPEN-LABEL; AUTOLOGOUS TRANSPLANTATION; LENALIDOMIDE MAINTENANCE; IMMUNOMODULATORY DRUGS; ANTITUMOR-ACTIVITY; PLUS POMALIDOMIDE;
D O I
10.2147/ITT.S240886
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The multiple myeloma (MM) therapeutic landscape has evolved significantly with the approval of numerous novel agents, including next generation proteasome inhibitors (PIs), immunomodulatory agents (IMIDs), and monoclonal antibodies (MoABs) targeting CD38 and SLAMF7. While these discoveries have led to an unprecedented improval in patient outcomes, the disease still remains incurable. Immunotherapeutic approaches have shown substantial promise in recent studies of chimeric antigen receptor T-cell (CAR T-cell) therapy, bispecific antibodies, and antibody drug conjugates targeting B-cell maturation antigen (BCMA). This review will highlight these novel and targeted therapies in MM, with particular focus on PIs, IMIDs, MoAb and BCMA-directed immunotherapy.
引用
收藏
页码:201 / 215
页数:15
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