TY - JOUR
T1 - Outcome of allogeneic bone marrow transplantation for children with advanced acute myeloid leukemia
AU - Nemecek, E. R.
AU - Gooley, T. A.
AU - Woolfrey, A. E.
AU - Carpenter, P. A.
AU - Matthews, D. C.
AU - Sanders, J. E.
N1 - Funding Information:
We thank Mr Paul Hoffmeister for his assistance in data collection. This work was supported in part by Grants CA100394 and CA18029 from the National Cancer Institute, National Institutes of Health.
PY - 2004/11
Y1 - 2004/11
N2 - Allogeneic bone marrow transplantation (BMT) may offer the only chance of cure for children with acute myeloid leukemia (AML) in second complete remission (CR2) or with relapsed disease, but the outcome of these patients has not been clearly defined. We conducted a retrospective study of 58 children, median age 7.4 years (range 0.8-17.3), who received matched related or unrelated BMT at our institution for AML in CR2 (n=12), in untreated first relapse (n=11) or with refractory disease (n=35), to identify risk factors associated with disease-free survival (DFS). Life threatening to fatal regimen-related toxicity was observed in 22% of patients. Estimates of DFS at 5 years (95% confidence interval) for patients in CR2, with untreated first relapse and refractory disease were 58% (27-80%), 36% (11-63%) and 9% (2-21%), respectively. Non-relapse mortality estimates were 0%, 27% (0-54%) and 17% (5-30%), and relapse estimates were 42% (14-70%), 36% (8-65%) and 74% (60-89%), respectively. Advanced disease phase and cytogenetic abnormalities at the time of transplantation were each associated with decreased DFS and increased relapse in multivariable regression models. Survival for children transplanted in CR2 or untreated first relapse is higher than that previously reported, but relapse remains the major cause of treatment failure regardless of disease stage.
AB - Allogeneic bone marrow transplantation (BMT) may offer the only chance of cure for children with acute myeloid leukemia (AML) in second complete remission (CR2) or with relapsed disease, but the outcome of these patients has not been clearly defined. We conducted a retrospective study of 58 children, median age 7.4 years (range 0.8-17.3), who received matched related or unrelated BMT at our institution for AML in CR2 (n=12), in untreated first relapse (n=11) or with refractory disease (n=35), to identify risk factors associated with disease-free survival (DFS). Life threatening to fatal regimen-related toxicity was observed in 22% of patients. Estimates of DFS at 5 years (95% confidence interval) for patients in CR2, with untreated first relapse and refractory disease were 58% (27-80%), 36% (11-63%) and 9% (2-21%), respectively. Non-relapse mortality estimates were 0%, 27% (0-54%) and 17% (5-30%), and relapse estimates were 42% (14-70%), 36% (8-65%) and 74% (60-89%), respectively. Advanced disease phase and cytogenetic abnormalities at the time of transplantation were each associated with decreased DFS and increased relapse in multivariable regression models. Survival for children transplanted in CR2 or untreated first relapse is higher than that previously reported, but relapse remains the major cause of treatment failure regardless of disease stage.
KW - Acute myeloid leukemia
KW - Childhood leukemia
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U2 - 10.1038/sj.bmt.1704689
DO - 10.1038/sj.bmt.1704689
M3 - Article
C2 - 15361903
AN - SCOPUS:7944220987
SN - 0268-3369
VL - 34
SP - 799
EP - 806
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 9
ER -