Bispecific Antibodies in Multiple Myeloma: Present and Future

被引:61
|
作者
Lancman, Guido [1 ]
Sastow, Dahniel L. [2 ]
Cho, Hearn J. [1 ]
Jagannath, Sundar [1 ]
Madduri, Deepu [1 ]
Parekh, Samir S. [1 ]
Richard, Shambavi [1 ]
Richter, Joshua [1 ]
Sanchez, Larysa [1 ]
Chari, Ajai [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
来源
BLOOD CANCER DISCOVERY | 2021年 / 2卷 / 05期
关键词
CELL MATURATION ANTIGEN; OPEN-LABEL; DARATUMUMAB MONOTHERAPY; PRECLINICAL ACTIVITY; PLUS BORTEZOMIB; FAMILY-MEMBER; HUMAN CD38; DEXAMETHASONE; RECEPTOR; THERAPY;
D O I
10.1158/2643-3230.BCD-21-0028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite many recent advances in therapy, there is still no plateau in overall survival curves in multiple myeloma. Bispecific antibodies are a novel immunotherapeutic approach designed to bind antigens on malignant plasma cells and cytotoxic immune effector cells. Early-phase clinical trials targeting B-cell maturation antigen (BCMA), GPRC5D, and FcRH5 have demonstrated a favorable safety profile, with mainly low-grade cytokine release syndrome, cytopenias, and infections. Although dose escalation is ongoing in several studies, early efficacy data show response rates in the most active dose cohorts between 61% and 83% with many deep responses; however, durability remains to be established. Further clinical trial data are eagerly anticipated. Significance: Overall survival of triple-class refractory multiple myeloma remains poor. Bispecific antibodies are a novel immunotherapeutic modality with a favorable safety profile and impressive preliminary efficacy in heavily treated patients. Although more data are needed, bispecifics will likely become an integral part of the multiple myeloma treatment paradigm in the near future. Studies in earlier lines of therapy and in combination with other active anti-multiple myeloma agents will help further define the role of bispecifics in multiple myeloma.
引用
收藏
页码:423 / 433
页数:11
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