Blood · 2011 · 173 citations · 43 references
MedicineHematologyPediatricsPediatric HematologyPediatric OncologyStem Cell TransplantationAllogeneic Stem Cell TransplantationHematopoietic Stem Cell TransplantationPediatric LeukemiasPediatric TransplantationTransplant OutcomesAcute Myeloid Leukemia TransplantationBone Marrow Donor SelectionLeukemia RiskPediatric Donor SelectionSuccess Rate AnalysisTransplantation For Hematologic MalignanciesTransplantation Outcome Assessment
We evaluated 190 children with very high-risk leukemia, who underwent allogeneic hematopoietic cell transplantation in 2 sequential treatment eras, to determine whether those treated with contemporary protocols had a high risk of relapse or toxic death, and whether non-HLA-identical transplantations yielded poor outcomes. For the recent cohorts, the 5-year overall survival rates were 65% for the 37 patients with acute lymphoblastic leukemia and 74% for the 46 with acute myeloid leukemia; these rates compared favorably with those of earlier cohorts (28%, n = 57; and 34%, n = 50, respectively). Improvement in the recent cohorts was observed regardless of donor type (sibling, 70% vs 24%; unrelated, 61% vs 37%; and haploidentical, 88% vs 19%), attributable to less infection (hazard ratio [HR] = 0.12; P = .005), regimen-related toxicity (HR = 0.25; P = .002), and leukemia-related death (HR = 0.40; P = .01). Survival probability was dependent on leukemia status (first remission vs more advanced disease; HR = 0.63; P = .03) or minimal residual disease (positive vs negative; HR = 2.10; P = .01) at the time of transplantation. We concluded that transplantation has improved over time and should be considered for all children with very high-risk leukemia, regardless of matched donor availability.
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Reduced Mortality after Allogeneic Hematopoietic-Cell Transplantation
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