Skip to main content
. 2021 Oct 26;9(10):e003428. doi: 10.1136/jitc-2021-003428

Table 1.

Baseline clinical characteristics and immunologic findings of the pre- and post-CAR-T-cell therapy cohorts

Demographics Diagnosis and treatments prior to CAR-T-cell therapy CAR-T-cell therapy and vaccine Baseline immunologic findings*
Study ID Age group, years Sex Underlying diagnosis† Prior HCT, months to vaccine mAb within prior 6 months before vaccine‡ CAR-Tx target§ Months, CAR-Tx to vaccine Vaccine type¶ IgG, mg/dL CD19+ B cells /µL CD4+ T cells /µL
Pre-CAR-T cohort
Individuals with an antibody response to ≥1 vaccine strain
Pre-4 18–60 F MM yes BCMA IIV4 21 21.0 470
Pre-5 61–75 M MM Auto, 43 yes BCMA IIV4 591 87.2 436
Individuals without antibody responses
Pre-1 18–60 M ALL yes CD19 IIV4 376 4.7 236
Pre-2 18–60 M NHL Auto, 19 CD20 IIV4 552 <0.1 103
Pre-3 18–60 M MM Auto, 32 BCMA IIV4 46 47.2 433
Post-CAR-T cohort
Individuals with an antibody response to ≥1 vaccine strain
Post-1 18–60 M ALL Allo, 50 CD19 16 IIV4 823 401.2 392
Post-4 18–60 F CLL CD19 50 ccIIV4 334 14.4 488
Post-11 61–75 M NHL CD19 50 ccIIV4 189 0 501
Post-13 61–75 M MM Auto, 86 BCMA 14 aIIV3 290 164.7 317
Individuals without antibody responses
Post-2 18–60 F ALL Allo, 31 CD19 13 ccIIV4 371 0 176
Post-3 18–60 F ALL Allo, 60 CD19 57 IIV4 310 <0.1 152
Post-5 61–75 M CLL CD19 54 IIV4 217 <0.1 480
Post-6 61–75 F CLL CD19 21 IIV3-HD 286 2.8 332
Post-7 18–60 M NHL CD19 19 IIV4** 527 <0.1 394
Post-8 18–60 M NHL CD19 19 IIV4 416 0.9 353
Post-9 18–60 F NHL Auto, 48 CD19 34 IIV4 447 94.7 504
Post-10 61–75 M NHL CD19 24 IIV4 364 207.3 303
Post-12 61–75 M NHL CD19 20 IIV 324 0.3 304

Additional information is provided in online supplemental tables 1 and 2. Blank fields indicate not applicable. Baseline is defined as the day of the baseline blood sample prior to vaccination.

*Lower limit of normal; IgG, 610 mg/dL; CD19+ B cells, 100 cells/µL; CD4+ T cells, 500 cells/µL.

†All individuals in the pre-CAR-T cohort had relapsed/refractory disease at baseline. All individuals in the post-CAR-T cohort had complete remission or very good partial remission at baseline.

‡Monoclonal antibodies were: ‘pre-1’, blinatumomab; ‘pre-4’ and ‘pre-5’, daratumumab.

§CAR-T-cell protocols are depicted in online supplemental table S1.

¶Vaccine strains were: A/Brisbane/02/2018 (H1N1)pdm09-like virus, A/Kansas/14/2017 (H3N2)-like virus, B/Colorado/06/2017-like virus (B/Victoria/2/87 lineage) for IIV3, with the addition of a B/Phuket/3073/2013-like virus (B/Yamagata/16/88 lineage) for IIV4.

**One of the 13 individuals in the post-CAR-T cohort did not receive an influenza vaccine in the prior season.

aIIV3, adjuvant trivalent inactivated influenza vaccine; ALL, acute lymphoblastic leukemia; Allo, allogeneic; Auto, autologous; BCMA, B cell maturation antigen; CAR-T-cell, chimeric antigen receptor-modified T cell; CAR-Tx, CAR-T-cell therapy; cc, cell culture based; CLL, chronic lymphocytic leukemia; F, female; HCT, hematopoietic cell transplant; HD, high dose; IIV3, trivalent inactivated influenza vaccine; IIV4, quadrivalent inactivated influenza vaccine; M, male; mAb, B cell lineage targeted monoclonal antibody; MM, multiple myeloma; NHL, non-Hodgkin's lymphoma.