GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR ASSOCIATED WITH INDUCTION TREATMENT OF ACUTE MYELOGENOUS LEUKEMIA - A RANDOMIZED TRIAL BY THE -ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER LEUKEMIA COOPERATIVE GROUP
R. Zittoun et al., GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR ASSOCIATED WITH INDUCTION TREATMENT OF ACUTE MYELOGENOUS LEUKEMIA - A RANDOMIZED TRIAL BY THE -ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER LEUKEMIA COOPERATIVE GROUP, Journal of clinical oncology, 14(7), 1996, pp. 2150-2159
Purpose: To assess the value of granulocyte-macrophage colony-stimulat
ing factor (GM-CSF) for induction treatment of acute myeloid leukemia
(AML), both for priming of leukemic cells and for acceleration of hema
topoietic recovery. Patients and Methods: GM-CSF was administered 5 mu
g/kg/d by continuous intravenous (IV) infusion during induction thera
py with daunorubicin (DNR) (days 1 to 3) and cytarabine (ARA-C) (days
1 to 7). A total of 102 patients were randomized onto four arms, as fo
llows: (1) GM-CSF 24 hours before and during chemotherapy (arm +/-); (
2) GM-CSF after chemotherapy until day 28 or recovery of polymorphonuc
lear leukocytes (PMNs) (arm -/+); (3) GMCSF before, during, and after
chemotherapy (arm +/+); or (4) no GM-CSF (arm -/-). Stopping rules wer
e applied in case of an initial WBC count greater than 30 x 10(9)/L or
ct secondary increase of circulating blast cells, Analyses were perfo
rmed according to the intention-to-treat principle. Results: The compl
ete remission (CR) rates were 77% (arm -/-), 72% (arm +/-), 48% (arm -
/+), and 46% (arm +/+). patients randomized to receive GM-CSF after in
duction (arms -/+ and +/+) had a significantly lower CR rate (P = .008
) and a trend toward accelerated recovery of neutrophils, but no fewer
infections or induction deaths. The lower CR rate appeared to be rela
ted to an increased resistance rate, with persistent leukemia. The mai
n side effects of GM-CSF were fluid retention and hypotension. Conclus
ion: GM-CSF administered during induction treatment of AML with a DNR/
Ara-C combination did not provide any clinical benefit. Furthermore, t
here wets a significant decrease in the CR rate with more persistent l
eukemia when GM-CSF was administered during the hypoplastic phase afte
r the chemotherapy courses.