Outcome Parameters After Allogeneic BMT for AML
. | AML 1st CR (n = 31) . | AML 2nd CR (n = 8) . |
---|---|---|
Engraftment | ||
Median transplant cell dose ×107/kg (range) | 2.68 (0.69-7.44) | 2.9 (1.08-4.60) |
Median days to sustained* ANC ≥500 (range) | 13 (11-19)† | 14 (11-21)‡ |
Median days to sustained1-153 platelet count ≥20,000 (range) | 24 [12-93] | 25 (15-43) |
Posttransplant EBV-LPD | 3 | 0 |
GVHD | ||
Acute, grade I | 2 | 0 |
Acute, grade II-IV | 0 | 0 |
Chronic | 21-155 | 0 |
Causes of death | ||
Relapse | 1 | 1 |
Infectious causes | 2 CMV pneumonitis¶ | 1 CMV pneumonitis |
1 fungal pneumonia | 1 toxoplasmosis | |
1 P carinii pneumonia | ||
GVHD and secondary complications | 1 | |
Secondary complications related to treatment of EBV-LPD | 1 | |
Other | 1 late IP | |
Alive and no evidence of disease | 24 | 4 |
Sustained complete donor chimerism in bone marrow | 23 | 4 |
Median f/u months (range) | 56.2 (28.4-66.2) | 47.5 (37.9-47.5) |
. | AML 1st CR (n = 31) . | AML 2nd CR (n = 8) . |
---|---|---|
Engraftment | ||
Median transplant cell dose ×107/kg (range) | 2.68 (0.69-7.44) | 2.9 (1.08-4.60) |
Median days to sustained* ANC ≥500 (range) | 13 (11-19)† | 14 (11-21)‡ |
Median days to sustained1-153 platelet count ≥20,000 (range) | 24 [12-93] | 25 (15-43) |
Posttransplant EBV-LPD | 3 | 0 |
GVHD | ||
Acute, grade I | 2 | 0 |
Acute, grade II-IV | 0 | 0 |
Chronic | 21-155 | 0 |
Causes of death | ||
Relapse | 1 | 1 |
Infectious causes | 2 CMV pneumonitis¶ | 1 CMV pneumonitis |
1 fungal pneumonia | 1 toxoplasmosis | |
1 P carinii pneumonia | ||
GVHD and secondary complications | 1 | |
Secondary complications related to treatment of EBV-LPD | 1 | |
Other | 1 late IP | |
Alive and no evidence of disease | 24 | 4 |
Sustained complete donor chimerism in bone marrow | 23 | 4 |
Median f/u months (range) | 56.2 (28.4-66.2) | 47.5 (37.9-47.5) |
*Sustained denotes 3 consecutive days.
Eleven of 31 patients received G-CSF (see text).
Five of 8 patients received G-CSF (see text).
Sustained denotes 3 consecutive days and platelet transfusion independent.
One of these two cases occurred solely as a complication of treatment of EBV-LPD with donor leukocytes (see text).
¶One of these two patients also had hepatic veno-occlusive disease.