Patient characteristics (n = 30)
. | No. of patients/No. of evaluable patients . | Mean . | Range . |
---|---|---|---|
Age, y | |||
<10 | 13 | 14 | 0.5-45 |
10-20 | 11 | ||
21-40 | 4 | ||
>40 | 2 | ||
Body weight, kg | 39 | 5-83 | |
Karnofsky index, % | 65 | 20-100 | |
Diagnosis | |||
Acute lymphoblastic leukemia | 14 | ||
Acute myeloid leukemia | 4 | ||
Chronic myeloid leukemia | 1 | ||
Myelodysplastic syndrome | 1 | ||
Solid tumor | 1 | ||
Immunodeficiency | 7 | ||
Congenital bone marrow failure | 1 | ||
Non-Hodgkin lymphoma | 1 | ||
Graft | |||
Matched unrelated donor | 7 | ||
Matched sibling donor | 3 | ||
Mismatched unrelated donor (<9/10 matched) | 3 | ||
Haploidentical HSCT from parents or siblings | 17 | ||
T-cell depletion | |||
In vivo depletion (ATG) | 7 | ||
Graft manipulation (plus serotherapy) | 17 | ||
Alemtuzumab | 4 | ||
Antiviral drugs for treatment of AdV | |||
Cidofovir | |||
Before ACT | 28/29 | ||
After ACT | 20/27 | ||
Ribavirin | 19/26 | ||
Time of first positive AdV PCR in days after HSCT | |||
In stool (n = 30) | 29 | –80-275 | |
In blood (n = 28) | 36 | –71-305 | |
Days to ACT after HSCT (± SD)] | 56 ± 61 | ||
<50 | 25 | ||
50-100 | 7 | ||
>100 | 6 |
. | No. of patients/No. of evaluable patients . | Mean . | Range . |
---|---|---|---|
Age, y | |||
<10 | 13 | 14 | 0.5-45 |
10-20 | 11 | ||
21-40 | 4 | ||
>40 | 2 | ||
Body weight, kg | 39 | 5-83 | |
Karnofsky index, % | 65 | 20-100 | |
Diagnosis | |||
Acute lymphoblastic leukemia | 14 | ||
Acute myeloid leukemia | 4 | ||
Chronic myeloid leukemia | 1 | ||
Myelodysplastic syndrome | 1 | ||
Solid tumor | 1 | ||
Immunodeficiency | 7 | ||
Congenital bone marrow failure | 1 | ||
Non-Hodgkin lymphoma | 1 | ||
Graft | |||
Matched unrelated donor | 7 | ||
Matched sibling donor | 3 | ||
Mismatched unrelated donor (<9/10 matched) | 3 | ||
Haploidentical HSCT from parents or siblings | 17 | ||
T-cell depletion | |||
In vivo depletion (ATG) | 7 | ||
Graft manipulation (plus serotherapy) | 17 | ||
Alemtuzumab | 4 | ||
Antiviral drugs for treatment of AdV | |||
Cidofovir | |||
Before ACT | 28/29 | ||
After ACT | 20/27 | ||
Ribavirin | 19/26 | ||
Time of first positive AdV PCR in days after HSCT | |||
In stool (n = 30) | 29 | –80-275 | |
In blood (n = 28) | 36 | –71-305 | |
Days to ACT after HSCT (± SD)] | 56 ± 61 | ||
<50 | 25 | ||
50-100 | 7 | ||
>100 | 6 |