TY - JOUR
T1 - Bispecific Antibodies in Multiple Myeloma
T2 - Present and Future
AU - Lancman, Guido
AU - Sastow, Dahniel L.
AU - Cho, Hearn J.
AU - Jagannath, Sundar
AU - Madduri, Deepu
AU - Parekh, Samir S.
AU - Richard, Shambavi
AU - Richter, Joshua
AU - Sanchez, Larysa
AU - Chari, Ajai
N1 - Publisher Copyright:
©2021 American Association for Cancer Research.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85115605575&partnerID=8YFLogxK
U2 - 10.1158/2643-3230.BCD-21-0028
DO - 10.1158/2643-3230.BCD-21-0028
M3 - Review article
C2 - 34661161
AN - SCOPUS:85115605575
SN - 2643-3249
VL - 2
SP - 423
EP - 433
JO - Blood cancer discovery
JF - Blood cancer discovery
IS - 5
ER -