| Literature DB >> 24888273 |
K Koh1, D Tomizawa2, A Moriya Saito3, T Watanabe4, T Miyamura5, M Hirayama6, Y Takahashi7, A Ogawa8, K Kato9, K Sugita10, T Sato11, T Deguchi6, Y Hayashi12, J Takita13, Y Takeshita14, M Tsurusawa15, K Horibe3, S Mizutani2, E Ishii16.
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.Entities:
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Year: 2014 PMID: 24888273 DOI: 10.1038/leu.2014.172
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528