| Literature DB >> 17252021 |
X Thomas1, E Raffoux, S de Botton, C Pautas, P Arnaud, T de Revel, O Reman, C Terré, B Corront, C Gardin, Q-H Le, B Quesnel, C Cordonnier, J-H Bourhis, M Elhamri, P Fenaux, C Preudhomme, M Michallet, S Castaigne, H Dombret.
Abstract
In a multicenter trial, 259 young adults (15-49 years) with newly diagnosed acute myeloid leukemia (AML) were first randomized to receive a timed-sequential induction regimen given either alone (135 patients) or concomitantly with granulocyte-macrophage colony-stimulating factor (GM-CSF) (124 patients). Patients reaching complete remission (CR) were then randomized to compare a timed-sequential consolidation to a postremission chemotherapy including four cycles of high-dose cytarabine followed by maintenance courses. In the appropriate arm, GM-CSF was given concurrently with chemotherapy during all cycles of consolidation. CR rates were significantly better in the GM-CSF arm (88 vs 78%, P<0.04), but did not differ after salvage. Patients receiving GM-CSF had a higher 3-year event-free survival (EFS) estimate (42 vs 34%), but GM-CSF did not impact on overall survival. Patients with intermediate-risk cytogenetics benefited more from GM-CSF therapy (P=0.05) in terms of EFS than patients with other cytogenetics. This was also confirmed when considering only patients following the second randomization, or subgroups defined by a prognostic index based on cytogenetics and the number of courses required for achieving CR. Priming of leukemic cells with hematopoietic growth factors is a means of enhancing the efficacy of chemotherapy in younger adults with AML.Entities:
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Year: 2007 PMID: 17252021 DOI: 10.1038/sj.leu.2404521
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528