Early use of allogeneic hematopoietic stem cell transplantation for infants with MLL gene-rearrangement-positive acute lymphoblastic leukemia

Leukemia. 2015 Feb;29(2):290-6. doi: 10.1038/leu.2014.172. Epub 2014 Jun 3.

Abstract

Sixty-two infants with MLL gene-rearrangement-positive acute lymphoblastic leukemia (MLL-r ALL) were treated with the MLL03 protocol of the Japanese Pediatric Leukemia/Lymphoma Study Group: short-course intensive chemotherapy followed by early allogeneic hematopoietic stem cell transplantation (HSCT) within 4 months of the initial induction. The 4-year event-free survival and overall survival rates were 43.2% (95% confidence interval (CI)=30.7-55.1%) and 67.2% (53.8-77.4%), respectively. A univariate analysis showed younger age (<90 days at diagnosis), central nervous system disease and poor response to initial prednisolone therapy significantly associated with poor prognosis (P<0.05). In a multivariate analysis, younger age at diagnosis tended to be associated with poor outcome (hazard ratio=1.969; 95% CI=0.903-4.291; P=0.088). Although the strategy of early use of HSCT effectively prevented early relapse and was feasible for infants with MLL-r ALL, the fact that substantial number of patients still relapsed even though transplanted in their first remission indicates the limited efficacy of allogeneic HSCT for infants with MLL-r ALL. Considering the risk of severe late effects, indications for HSCT should be restricted to specific subgroups with poor risk factors. An alternative approach incorporating molecular-targeted drugs should be established.

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Child, Preschool
  • Disease-Free Survival
  • Female
  • Gene Rearrangement*
  • Hematopoietic Stem Cell Transplantation*
  • Histone-Lysine N-Methyltransferase
  • Humans
  • Infant
  • Male
  • Multivariate Analysis
  • Myeloid-Lymphoid Leukemia Protein / genetics*
  • Neoplasm Recurrence, Local / therapy
  • Neoplasm, Residual
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / therapy*
  • Prednisolone / therapeutic use
  • Prognosis
  • Proportional Hazards Models
  • Recurrence
  • Risk Factors
  • Transplantation, Homologous
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • KMT2A protein, human
  • Myeloid-Lymphoid Leukemia Protein
  • Prednisolone
  • Histone-Lysine N-Methyltransferase