Table 3.

Incidence of hematological toxicities on bispecifics for multiple myeloma published trials

ReferencePopulationDrug/targetN*Anemia&Neutropenia&Thrombocytopenia&Febrile Neutropenia&Lymphopenia&Low IgG&HLH&DIC&
Usmani et al. (2021)27  Adult R/R MM Teclistamab BCMA × CD3 40 20(50%)/ 11(28%) 26(65%)/ 16(40%) 18(45%)/8(20%) NA/NA 7(9.6%)/ 7(9.6%) 14(9%)/NA NA/NA NA/NA 
Moreau et al. (2022)28 ¥ Adult R/R MM Teclistamab BCMA × CD3 165 86(52.1%)/ 61(37%) 117(70.9%)/ 106(64%) 66(40%)/35(21%) 4(2.4%)/NA 57(34.5%)/ 54(32.7%) 123(74.5%)/NA NA/NA NA/NA 
D'Souza et al. (2022)31  Adult R/R MM ABBV-383
BCMA × CD3 
124 36(29%)/ 20(16%) 46(37%)/ 42(34%) 29(23%)/15(12%) NA/NA 19(15%)/16(13%) 17(14%)/NA NA/NA NA/NA 
Chari et al. (2022)33 # Adult R/R MM Talquetamab GPRC5D × CD3 130 63(48.5%)/ 36(27.7%) 67(51.5%)/ 59(45.4%) 39(30%)/26(20%) NA/3(2.3%) 42(32.3%)/ 42(32.3%) NA/NA NA/NA NA/NA 
ReferencePopulationDrug/targetN*Anemia&Neutropenia&Thrombocytopenia&Febrile Neutropenia&Lymphopenia&Low IgG&HLH&DIC&
Usmani et al. (2021)27  Adult R/R MM Teclistamab BCMA × CD3 40 20(50%)/ 11(28%) 26(65%)/ 16(40%) 18(45%)/8(20%) NA/NA 7(9.6%)/ 7(9.6%) 14(9%)/NA NA/NA NA/NA 
Moreau et al. (2022)28 ¥ Adult R/R MM Teclistamab BCMA × CD3 165 86(52.1%)/ 61(37%) 117(70.9%)/ 106(64%) 66(40%)/35(21%) 4(2.4%)/NA 57(34.5%)/ 54(32.7%) 123(74.5%)/NA NA/NA NA/NA 
D'Souza et al. (2022)31  Adult R/R MM ABBV-383
BCMA × CD3 
124 36(29%)/ 20(16%) 46(37%)/ 42(34%) 29(23%)/15(12%) NA/NA 19(15%)/16(13%) 17(14%)/NA NA/NA NA/NA 
Chari et al. (2022)33 # Adult R/R MM Talquetamab GPRC5D × CD3 130 63(48.5%)/ 36(27.7%) 67(51.5%)/ 59(45.4%) 39(30%)/26(20%) NA/3(2.3%) 42(32.3%)/ 42(32.3%) NA/NA NA/NA NA/NA 

DIC, disseminated intravascular coagulation; HLH, hemophagocytic lymphohystiocytosis; MM, multiple myeloma; NA, not available; R/R, relapsed/refractory; RP2P, recommended phase 2 dose.

*

N is the population considered for that extracted data, which may be the whole cohort or a subpopulation.

&

Adverse event, any grade(%)/grade ≥3(/%).

¥

Data from cohort of phase 1 and cohort of phase 2 that used the RP2D; N  =  165.

#

Data from all subcutaneous cohorts (supplement material); N  =  130.

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