Patient characteristics
. | T-cell–depleted SCT patients without EBV-LPD (n = 20) . | T-cell–depleted SCT patients with EBV-LPD (n = 6) . |
---|---|---|
Age, y | ||
Mean (range) | 7.3 (1-16) | 6.6 (1-13) |
Diagnosis, n | ||
ALL CR1 | 3 | |
ALL CR2 | 4 | 1 |
AML CR1 | 1 | 1 |
FEL | 2 | 1 |
SAA | 1 | 2 |
Fanconi | 1 | |
MLD | 1 | |
X-ALD | 2 | |
Hurler-Scheie | 1 | |
SCID | 1 | 1 |
JMML/CML | 2 | |
MDS | 1 | |
Donor type, n | ||
MUD | 12 | 4 |
Haplo | 8 | 2 |
Conditioning includes, n | ||
ATG | 3 | 1 |
Campath-1H | 2 | 1 |
ATG + anti-LFA-1 | 3 | 2 |
Campath-1H + anti-LFA-1 | 11 | 1 |
Positive EBV serology, n | ||
D/R | 20/14 | 6/3 |
Stem cell graft preparation, n | ||
CD34+ selection | 7 | 2 |
T and B immunorosetting | 12 | 3 |
Other* | 1 | 1 |
. | T-cell–depleted SCT patients without EBV-LPD (n = 20) . | T-cell–depleted SCT patients with EBV-LPD (n = 6) . |
---|---|---|
Age, y | ||
Mean (range) | 7.3 (1-16) | 6.6 (1-13) |
Diagnosis, n | ||
ALL CR1 | 3 | |
ALL CR2 | 4 | 1 |
AML CR1 | 1 | 1 |
FEL | 2 | 1 |
SAA | 1 | 2 |
Fanconi | 1 | |
MLD | 1 | |
X-ALD | 2 | |
Hurler-Scheie | 1 | |
SCID | 1 | 1 |
JMML/CML | 2 | |
MDS | 1 | |
Donor type, n | ||
MUD | 12 | 4 |
Haplo | 8 | 2 |
Conditioning includes, n | ||
ATG | 3 | 1 |
Campath-1H | 2 | 1 |
ATG + anti-LFA-1 | 3 | 2 |
Campath-1H + anti-LFA-1 | 11 | 1 |
Positive EBV serology, n | ||
D/R | 20/14 | 6/3 |
Stem cell graft preparation, n | ||
CD34+ selection | 7 | 2 |
T and B immunorosetting | 12 | 3 |
Other* | 1 | 1 |
ALL CR1 indicates acute lymphoblastic leukemia first remission; AML CR1, acute myeloblastic leukemia first remission; FEL, familial erythrophagocytic lymphhistiocytosis; SAA, severe aplastic leukemia; MLD, metachromatic leukodystrophy; X-ALD, X-linked adrenoleukodystrophy; JMML/CML, juvenile myelomonocytic leukemia/chronic myeloid leukemia; MDS, myelodysplastic syndrome; LFA-1, lymphocyte junction-associated antigen type 1; D/R, donor recipient.
Campath-1G in the bag and E-rosetting, respectively.