Table 8.

Incidence of infections with BCMA-directed CAR T-cell therapies as reported in clinical studies (A) and in retrospective real-world series (B) (Continued)

8B
Real-world cohortsNumber of patientsTime frameOverall grade (%)Bacterial (%)Viral (%)Fungal (%)Respiratory infection
Kambhampti76  55 12 mo 47 infections in 29 patients (53%) 40 53 68 
Logue77  52 100 d 46 infectious events in 28 patients (54%) 59 35 59 
Wang78  40 Until last FU; median FU 16 mo 44 infectious events in 23 patients (58%) 57 18 73 
Josyula79  32 180 d 23 infectious events in 17 patients (53%) 30 61 NR 
Mohan71  26 Median FU 9 mo 5 patients with infection (19%) NR NR NR NR 
Mikkilineni80  24 30 d 10 infectious events in 9 patients (38%) 90 10 NR 
Little81  99 365 d d 1-100; 42 infectious events in 26 patients (26%)
d 101-365; 22 infectious events in 15 patients (15%) 
69
27 
17
41 
7
a
b 
8B
Real-world cohortsNumber of patientsTime frameOverall grade (%)Bacterial (%)Viral (%)Fungal (%)Respiratory infection
Kambhampti76  55 12 mo 47 infections in 29 patients (53%) 40 53 68 
Logue77  52 100 d 46 infectious events in 28 patients (54%) 59 35 59 
Wang78  40 Until last FU; median FU 16 mo 44 infectious events in 23 patients (58%) 57 18 73 
Josyula79  32 180 d 23 infectious events in 17 patients (53%) 30 61 NR 
Mohan71  26 Median FU 9 mo 5 patients with infection (19%) NR NR NR NR 
Mikkilineni80  24 30 d 10 infectious events in 9 patients (38%) 90 10 NR 
Little81  99 365 d d 1-100; 42 infectious events in 26 patients (26%)
d 101-365; 22 infectious events in 15 patients (15%) 
69
27 
17
41 
7
a
b 
a

Plus 7% pneumonia not otherwise specified. Overall, 13 of 42 (31%) of early infectious events were respiratory infections involving the lungs, upper respiratory tract, or sinuses.

b

Plus 32% pneumonia not other specified. Overall 17 of 22 (77%) of late infectious events were composed of respiratory infections involving the lungs, upper respiratory tract, or sinuses.

FU, follow-up.

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