TY - JOUR
T1 - Tacrolimus (FK506) and methotrexate as prophylaxis for acute graft-versus-host disease in pediatric allogeneic stem cell transplantation
AU - Yanik, G.
AU - Levine, J. E.
AU - Ratanatharathorn, V.
AU - Dunn, R.
AU - Ferrara, J.
AU - Hutchinson, R. J.
PY - 2000
Y1 - 2000
N2 - Currently, limited data exist on the role of tacrolimus (FK506) in pediatric allogeneic marrow transplantation. Forty-one patients who received tacrolimus as prophylaxis were reviewed, with a median age of 9 years (range 0.2-16 years). Twenty-one patients underwent related donor transplants and 20 underwent unrelated donor transplants. All patients received tacrolimus beginning the day prior to transplant at a dose of 0.03 mg/kg/day by continuous i.v. infusion. When clinically possible, patients were switched to oral therapy in two divided doses, at four times the intravenous dose. Tacrolimus levels were monitored twice a week, and dosages adjusted to maintain serum levels 5-15 ng/ml. Common adverse effects included hypomagnesemia (98%), hypertension (49%), nephrotoxicity (34%), and tremors (32%). Less common side-effects (< 10% cases) included seizures and hyperglycemia. The median time to ANC recovery (ANC > 500 x 106/l) was 15 days. For the related donor group, the incidence of grade II-IV acute GVHD was 33%, and grade III-IV GVHD 19%. For the unrelated donor group, the incidence of grade II-IV acute GVHD was 55%, and grade III-IV GVHD 30%. Overall, tacrolimus therapy was well tolerated as prophylaxis for acute GVHD in pediatric patients undergoing allogeneic transplantation.
AB - Currently, limited data exist on the role of tacrolimus (FK506) in pediatric allogeneic marrow transplantation. Forty-one patients who received tacrolimus as prophylaxis were reviewed, with a median age of 9 years (range 0.2-16 years). Twenty-one patients underwent related donor transplants and 20 underwent unrelated donor transplants. All patients received tacrolimus beginning the day prior to transplant at a dose of 0.03 mg/kg/day by continuous i.v. infusion. When clinically possible, patients were switched to oral therapy in two divided doses, at four times the intravenous dose. Tacrolimus levels were monitored twice a week, and dosages adjusted to maintain serum levels 5-15 ng/ml. Common adverse effects included hypomagnesemia (98%), hypertension (49%), nephrotoxicity (34%), and tremors (32%). Less common side-effects (< 10% cases) included seizures and hyperglycemia. The median time to ANC recovery (ANC > 500 x 106/l) was 15 days. For the related donor group, the incidence of grade II-IV acute GVHD was 33%, and grade III-IV GVHD 19%. For the unrelated donor group, the incidence of grade II-IV acute GVHD was 55%, and grade III-IV GVHD 30%. Overall, tacrolimus therapy was well tolerated as prophylaxis for acute GVHD in pediatric patients undergoing allogeneic transplantation.
KW - Allogeneic bone marrow transplant
KW - Children
KW - FK506
KW - Graft-versus-host disease
KW - Peripheral blood stem cell transplant
KW - Tacrolimus
UR - http://www.scopus.com/inward/record.url?scp=0033916073&partnerID=8YFLogxK
U2 - 10.1038/sj.bmt.1702472
DO - 10.1038/sj.bmt.1702472
M3 - Article
C2 - 10918426
AN - SCOPUS:0033916073
SN - 0268-3369
VL - 26
SP - 161
EP - 167
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 2
ER -