TY - JOUR
T1 - Effect of priming with granulocyte-macrophage colony-stimulating factor in younger adults with newly diagnosed acute myeloid leukemia
T2 - A trial by the Acute Leukemia French Association (ALFA) Group
AU - Thomas, X.
AU - Raffoux, E.
AU - de Botton, S.
AU - Pautas, C.
AU - Arnaud, P.
AU - de Revel, T.
AU - Reman, O.
AU - Terré, C.
AU - Corront, B.
AU - Gardin, C.
AU - Le, Q. H.
AU - Quesnel, B.
AU - Cordonnier, C.
AU - Bourhis, J. H.
AU - Elhamri, M.
AU - Fenaux, P.
AU - Preudhomme, C.
AU - Michallet, M.
AU - Castaigne, S.
AU - Dombret, H.
N1 - Funding Information:
This work was supported in part by Schering Plough (Kenilworth, NJ, USA) and Amgen (Neuilly sur Seine, France) which provided grants to the Edouard Herriot Hospital (Department of Hematology) for central data management. Schering Plough provided molgramostim (GM-CSF) free of charge.
PY - 2007/1/1
Y1 - 2007/1/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=33847202969&partnerID=8YFLogxK
U2 - 10.1038/sj.leu.2404521
DO - 10.1038/sj.leu.2404521
M3 - Article
C2 - 17252021
AN - SCOPUS:33847202969
SN - 0887-6924
VL - 21
SP - 453
EP - 461
JO - Leukemia
JF - Leukemia
IS - 3
ER -