M. Puntous et al., TREATMENT OF RELAPSED ACUTE MYELOID-LEUKEMIA USING GM-CSF BEFORE INTENSIVE CHEMOTHERAPY, Leukemia & lymphoma, 12(1-2), 1993, pp. 95-102
Ten patients with acute myeloblastic leukemia (AML) in first relapse w
ere treated with high-dose cytosine-arabinoside (ara-C, 3 g/m2/12 hour
s x 4) and amsacrine (150 mg/m2/day x 5). In order to prime the cells,
the patients were given rh-GM-CSF (3 mug/kg/d) for four days, the fir
st infusion starting 48 hours before chemotherapy. Two patients died d
uring the aplastic phase, seven patients achieved a second complete re
mission (CR2) and one patient remained leukemic. The median duration o
f aplasia was 17 days (14-21). These results were comparable to those
obtained in our previous series of 27 patients treated for AML in firs
t relapse with the same chemotherapy but without GM-CSF (66% CR2). Aft
er 48 hours of GM-CSF infusion, (before chemotherapy was started), sev
en patients had an increase in the white blood cell count with an incr
ease in the absolute number of blast cells in five of these cases. Mar
row blast cells percentages increased in 3 of the 8 patients analysed.
Six of seven patients tested showed an increase in the percentage of
cells in S-phase (studied by flow cytometry using the bromodeoxyuridin
e (BrdU/DNA) labelling technique and BrdU incorporation). GM-CSF used
to prime leukemic cells may be safely administered but its clinical us
efulness needs to be further evaluated.