Skip to main content
letter
. 2022 Sep 15;7(9):1849–1853. doi: 10.1182/bloodadvances.2022008338

Table 1.

Baseline demographics and clinical characteristics of the pre– and post–CAR-Tx cohorts (N = 45)

Baseline characteristics Cohort
Pre–CAR-Tx (n = 21) Post–CAR-Tx (n = 24)
Age, y (range) 67 (41-84) 59 (39-81)
Sex, n (%)
 Male 14 (66.7) 15 (62.5)
Race, n (%)
 White 19 (90.5) 24 (100)
Disease, n (%)
 Lymphoma 16 (76.2) 15 (62.5)
 ALL 0 1 (4.2)
 CLL 0 2 (8.3)
 MM 3 (14.3) 6 (25.0)
 WM 2 (9.5) 0
Target, n (%)
 CD19 15 (71.4) 16 (66.7)
 CD20 3 (14.3) 2 (8.3)
 BCMA 3 (14.3) 6 (25.0)
CAR-Tx type, n (%)
 Commercial 16 (76.2) 6 (25.0)
 Investigational 5 (23.8) 18 (75.0)
Vaccine type, n (%)
 mRNA-1273 6 (28.6) 12 (50.0)
 BNT162b2 15 (71.4) 12 (50.0)
IgG level, median (IQR), mg/dL 458 (363-552)
CD-19+ B cells, median (IQR), cells/mL 17 (0-160)
CD-4+ T cells, median (IQR), cells/mL 345 (219-559)
Time from second vaccine to sample collection, mo, median (IQR) 4.1 (1.9-5.4) 2.0 (0.7-2.4)
Time from CAR-Tx to second vaccination, mo, median (IQR) −4.3 (−5.9 to −2.4) 19.0 (10.5-29.2)
Time interval between first and second vaccination, d, median (IQR) 21 (21-28) 28 (21-29)
Time interval between second and third vaccination, d, median (IQR) 142 (117-206)

ALL, acute lymphoblastic leukemia; BCMA, B-cell maturation antigen; CLL, chronic lymphocytic leukemia; IQR, interquartile range; MM, multiple myeloma; WM, Waldenström macroglobulinemia.

Obtained at the time of the first prevaccine blood draw.

Among 15 individuals who received a third dose.