Table 1 Baseline characteristics and most reported adverse events in BCMA directed immunotherapy in patients with relapsed and/or refractory multiple myeloma.

From: Adverse effects and non-relapse mortality of BCMA directed T cell therapies in multiple myeloma: an FAERS database study

Characteristic

Ide-cel

Cilta-cel

Teclistamab

Number of patients

584

477

723

Number of adverse events reported

2132

874

1363

Age- yrs. median (interquartile)

66 (58.5–71)

66 (57.8–71)

65 (57–72)

Female (%)a

225 (38.5)

117 (24.5)

229 (31.8)

Death (%)a

68 (11.6)

82 (17.2)

159 (22.1)

Life threatening (%)a

43 (7.4)

42 (8.8)

81 (11.3)

Hospitalization (%)a

208 (35.6)

226 (47.4)

385 (53.5)

CRS (%)a

344 (16.1)

90 (10.3)

130 (9.5)

ICANS (%)a

80 (3.8)

29 (3.3)

34 (2.5)

Non-ICANS neurotoxicity (%)a

215 (10.1)

56 (6.4)

52 (3.8)

Pneumonia (%)a

4 (0.2)

20 (2.3)

63 (4.6)

Sepsis (%)a

15 (0.7)

17 (2.0)

46 (3.4)

COVID-19 infection (%)a

4 (0.2)

24 (2.7)

69 (5.0)

Infection (%)a

4 (0.2)

2 (0.2)

19 (1.4)

  1. Per 21CFR314.80, Life threatening event are defined as any adverse drug experience that places the patient, in the view of the initial reporter, at immediate risk of death from the adverse drug experience as it occurred, i.e., it does not include an adverse drug experience that, had it occurred in a more severe form, might have caused death.
  2. aN (%)