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. 2023 Aug 3;13:1229655. doi: 10.3389/fonc.2023.1229655

Table 1.

Demographics of immunocompromised pediatric patients who received T-C.

Variables n=24
Age (median [range]) 16.50 [12 – 21]
Gender (%) Female 14 (58.3)
Male 10 (41.7)
Race (%) Black or African American 7 (29.2)
Other 2 (8.3)
White 15 (62.5)
Ethnicity (%) Hispanic 7 (29.2)
Not Hispanic 17 (70.8)
Diagnosis (%) Mixed phenotype leukemia 1 (4.2)
ALL 6 (25.0)
AML 7 (29.2)
Hematologic Disease 10 (41.7)
Reason to receive T-C < 100 days from allogenic HCT
Graft versus host disease
Post CAR-T therapy
Chemotherapy
Other*
13 (54.2)
4 (16.7)
3 (12.5)
2 (8.3)
2 (8.3)
SARS-CoV-2 Vaccination Received
Pfizer-BioNTech (%) No 4 (16.7)
Yes 20 (83.3)
Moderna (%) No 15 (62.5)
Yes 9 (37.5)
Janssen (%) No 20 (83.3)
Yes 4 (16.7)
Received > 2 doses of vaccine (%) No 7 (29.2)
Yes 17 (70.8)
Number of vaccine doses/patient before T-C (median [range]) 2 [0 – 3]
SARS-CoV-2 infection before T-C dose infection, no. (%) No 22 (91.7)
Yes 2 (8.3)
Time between SARS-CoV-2 infection and first dose T-C (median [range]) 63.50 [6–121]
Platelet count prior to any T-C dose (median [range] 103/ mm3) 170 [25-561]
SARS-CoV-2 infection <=180 days from any T-C dose No 17 (70.8)
Yes 7 (29.2)
Time between any dose T-C and SARS-CoV-2 infection (median [range]) 102 [28–135]

*Other: Lupus on immunosuppressive therapy (n=1); Kidney transplant recipient on immunosuppressive therapy ^ Hematologic diseases: Aplastic Anemia (n=4), Sickle Cell Disease (n=4), Acquired Factor II deficiency (n=1), Myelodysplastic Syndrome (n=1).