TY - JOUR
T1 - Methotrexate vs cyclosporin A as a single agent for graft-versus-host disease prophylaxis in pediatric patients with hematological malignancies undergoing allogeneic bone marrow transplantation from HLA-identical siblings
T2 - A single-center analysis in Japan
AU - Koga, Y.
AU - Nagatoshi, Y.
AU - Kawano, Y.
AU - Okamura, J.
PY - 2003/7
Y1 - 2003/7
N2 - The efficacy of methotrexate (MTX) as a single graft-versus-host disease (GVHD) prophylaxis agent was compared to that of cyclosporin A (CSA) in 62 pediatric patients (median age: 8 years) with hematological malignancies who had undergone bone marrow transplantation (BMT) from HLA-identical sibling donors at National Kyushu Cancer Center since 1977. In all, 30 patients received MTX by intravenous bolus injection, with a dose of 15 mg/m2 on day + 1, followed by 10 mg/m2 on days + 3, + 6, and + 11, and then once a week until day + 100. A total of 32 patients were treated with CSA, which was given intravenously in the early stages and orally thereafter until day + 100, and then gradually tapered and stopped 6 months after BMT. There were no differences between the groups in terms of rates of hematopoietic recovery after BMT. The probabilities of acute GVHD (grades II-V) and chronic GVHD were 29.6 vs 40.6% (P = 0.294) and 19 vs 20% (MTX vs CSA), respectively. Relapse rates and event-free survival were identical. These results suggest that MTX and CSA were equally effective when given after BMT in Japanese pediatric patients with hematological malignancies. Since MTX was given over a shorter time than CSA, it might be more practical in the management of such patients.
AB - The efficacy of methotrexate (MTX) as a single graft-versus-host disease (GVHD) prophylaxis agent was compared to that of cyclosporin A (CSA) in 62 pediatric patients (median age: 8 years) with hematological malignancies who had undergone bone marrow transplantation (BMT) from HLA-identical sibling donors at National Kyushu Cancer Center since 1977. In all, 30 patients received MTX by intravenous bolus injection, with a dose of 15 mg/m2 on day + 1, followed by 10 mg/m2 on days + 3, + 6, and + 11, and then once a week until day + 100. A total of 32 patients were treated with CSA, which was given intravenously in the early stages and orally thereafter until day + 100, and then gradually tapered and stopped 6 months after BMT. There were no differences between the groups in terms of rates of hematopoietic recovery after BMT. The probabilities of acute GVHD (grades II-V) and chronic GVHD were 29.6 vs 40.6% (P = 0.294) and 19 vs 20% (MTX vs CSA), respectively. Relapse rates and event-free survival were identical. These results suggest that MTX and CSA were equally effective when given after BMT in Japanese pediatric patients with hematological malignancies. Since MTX was given over a shorter time than CSA, it might be more practical in the management of such patients.
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U2 - 10.1038/sj.bmt.1704051
DO - 10.1038/sj.bmt.1704051
M3 - Article
C2 - 12838282
AN - SCOPUS:0041368373
SN - 0268-3369
VL - 32
SP - 171
EP - 176
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 2
ER -