Table 4.

Response rates and key toxicities reported from pivotal BCMA-targeting trials and real-world data

Generic nameCommercial nameORR, %Median DORCRS rates: Any grade (≥3), %Neuro toxicity rates: Any grade (≥3), %FDA approvedReference
Idecabtagene vicleucel (ide-cel, also called bb2121) Abecma 73 10.7 mo 84 (5) 18 (3) Yes 58,61  
Real-World Consortium Data (ide-cel) Abecma 83 NR 82 (5) 15 (5) NA 116  
Ciltacabtagene autoleucel (cilta-cel) Carvikty 97 21.8 mo 95 (4) 21 (9) Yes 60,62  
Meta-analysis BCMA-directed CAR-T including those in trial phase NA 78-85 14 mo* NR (6.4-6.6)
 
NR (2.2-3.5) NA 117,118  
Teclistamab Tecvayli 63 18.4 mo 72.1 (0.6) 14.5 (0.6) Pending decision at time of writing 67  
DOR, duration of response; FDA, Food and Drug Administration; NA, not applicable. 
Generic nameCommercial nameORR, %Median DORCRS rates: Any grade (≥3), %Neuro toxicity rates: Any grade (≥3), %FDA approvedReference
Idecabtagene vicleucel (ide-cel, also called bb2121) Abecma 73 10.7 mo 84 (5) 18 (3) Yes 58,61  
Real-World Consortium Data (ide-cel) Abecma 83 NR 82 (5) 15 (5) NA 116  
Ciltacabtagene autoleucel (cilta-cel) Carvikty 97 21.8 mo 95 (4) 21 (9) Yes 60,62  
Meta-analysis BCMA-directed CAR-T including those in trial phase NA 78-85 14 mo* NR (6.4-6.6)
 
NR (2.2-3.5) NA 117,118  
Teclistamab Tecvayli 63 18.4 mo 72.1 (0.6) 14.5 (0.6) Pending decision at time of writing 67  
DOR, duration of response; FDA, Food and Drug Administration; NA, not applicable. 
*

Median PFS, not DOR reported.

or Create an Account

Close Modal
Close Modal