Table 1.
Characteristic | N = 26 |
---|---|
Sex, n (%) | |
Male | 14 (54) |
Female | 12 (46) |
Median age, y (range) | 59.5 (14-76) |
Race, n (%) | |
Caucasian | 18 (69) |
Black or African American | 3 (12) |
Multiracial | 1 (4) |
Native Hawaiian or other Pacific Islander | 1 (4) |
Unknown or unspecified | 3 (12) |
Ethnicity, n (%) | |
Not Hispanic or Latino | 19 (73) |
Hispanic or Latino | 7 (27) |
Diagnosis, (%) | |
Acute myeloid leukemia | 8 (31) |
Acute lymphoblastic leukemia | 5 (19) |
Chronic myeloid leukemia | 2 (8) |
Chronic lymphocytic leukemia | 1 (4) |
Myelodysplasia/myeloproliferative | 3 (12) |
Sickle cell anemia | 2 (8) |
Multiple myeloma | 1 (4) |
Other∗ | 4 (15) |
Transplant type, n (%) | |
Haploidentical | 12 (46) |
Mismatched unrelated | 9 (35) |
Matched unrelated with T-cell depletion | 4 (15) |
Umbilical cord blood | 1 (4) |
Preconditioning type, n (%) | |
Myeloablative | 12 (46) |
Reduced intensity/nonmyeloablative | 14 (54) |
CMV donor (D)/recipient (R) serostatus, n (%) | |
D−/R+ | 7 (27) |
D+R+ | 9 (35) |
D+/R− | 3 (12) |
D−/R−† | 7 (27) |
Receiving letermovir at baseline, n (%) | 16 (62) |
GVHD prophylaxis, n (%) | |
ATG | 4 (15) |
PTCy | 21 (81) |
Viremia at study day 1, n (%)‡ | |
BKV | 8 (31) |
HHV-6 | 5 (19) |
EBV | 2 (8) |
AdV | 1 (4) |
None | 14 (54) |
Adrenoleukodystrophy, cutaneous γ-δ T-cell lymphoma, diffuse large B-cell lymphoma, T-cell prolymphocytic leukemia.
One patient was reported as CMV D−/R− but had CMV viremia. Upon investigation by the site, the patient was previously reported as R+ but was presumed to have lost their CMV antibody positivity in a prior chimeric antigen receptor T-cell process.
Eight patients had viremia with a single virus (BKV, n = 4; HHV-6, n = 3; and EBV, n = 1), and 4 had viremia with 2 viruses (BKV + HHV-6, n = 2; AdV + BKV, n = 1; and BKV + EBV, n = 1).